Skip to main navigation Skip to main content
  • KSPTM
  • E-Submission

PHD : Parasites, Hosts and Diseases

OPEN ACCESS
ABOUT
BROWSE ARTICLES
FOR CONTRIBUTORS

Page Path

62
results for

"diagnosis"

Article category

Keywords

Publication year

Authors

Funded articles

"diagnosis"

Case Report

Amoebic enteritis: A clinicopathological analysis of 14 cases and literature review
Lining Wang, Linghong Kong, Yang Jiao, Jun Li, Xinpeng Zhang, Huizhong Xue, Xiaogang Liu
Parasites Hosts Dis 2025;63(2):168-173.
Published online May 26, 2025
DOI: https://doi.org/10.3347/PHD.24081
Amoebic enteritis is often misdiagnosed or overlooked due to its nonspecific clinical presentation. This study presents a comprehensive clinicopathological analysis of 14 confirmed cases of amoebic enteritis, examining their clinical manifestations, histopathological features, and responses to treatment. Periodic acid-Schiff and hexamine silver stains were employed to aid in diagnosis. A review of the relevant literature is also included to improve recognition and diagnostic accuracy of this uncommon but clinically significant condition.
  • 1,926 View
  • 34 Download

Brief Communications

Prevalence of asymptomatic malaria in high- and low-transmission areas of Tanzania: The role of asymptomatic carriers in malaria persistence and the need for targeted surveillance and control efforts
Ernest Mazigo, Hojong Jun, Wang-Jong Lee, Johnsy Mary Louis, Fadhila Fitriana, Jadidan Hada Syahada, Fauzi Muh, Feng Lu, Md Atique Ahmed, Seok Ho Cha, Wanjoo Chun, Won Sun Park, Se Jin Lee, Sunghun Na, Joon-Hee Han, Nyalali Kija, Smart Geodfrey, Eun-Teak Han, Jim Todd, Alphaxard Manjurano, Winifrida Kidima, Jin-Hee Han
Parasites Hosts Dis 2025;63(1):57-65.
Published online February 25, 2025
DOI: https://doi.org/10.3347/PHD.24077
As many countries implement different programs aimed at eliminating malaria, attention should be given to asymptomatic carriers that may interrupt the progress. This was a community-based cross-sectional study conducted in Tanzania from December 2022 to July 2023 within 4 villages from each of the 3 regions, Geita and Kigoma, which are high malaria transmission, and Arusha, which is low transmission. Malaria was diagnosed in asymptomatic individuals aged 1 year and older using the malaria rapid diagnostic test and light microscope. A total of 2,365 of 3,489 (67.9%) participants were enrolled from high-transmission villages. The overall prevalence was 25.5% and 15.8% by malaria rapid diagnostic test and light microscope, respectively. Using the respective tools, the prevalence was significantly higher at 35.6% (confidence interval (CI)=23.6–49.9) and 23.1% (CI=16.2–35.1) in the high-transmission regions (Geita and Kigoma) compared with 2.9% (CI=1.1–3.5) and 1.1% (CI=0.7–1.8) in the low-transmission region (Arusha). Children younger than 15 years and males accounted for the greatest proportion of infections. In the study area, the prevalence of asymptomatic cases was higher than that of reported symptomatic cases in health facilities. We hypothesize that these parasite reservoirs may contribute to the persistence of malaria in the country. Therefore, to achieve comprehensive malaria control in the country, the surveillance and screening of asymptomatic malaria cases are vital.

Citations

Citations to this article as recorded by  Crossref logo
  • Hidden reservoirs of infection: prevalence and risk factors of asymptomatic malaria in a high-endemic region of Zambia
    Wisdom Silwamba, David Chisompola, John Nzobokela, Martin Chakulya, Lombe Kabwe, Kingsley Tembo
    Malaria Journal.2025;[Epub]     CrossRef
  • Emergence of chloroquine-sensitive Plasmodium falciparum and rising resistance to first-line artemisinin partner drugs in Malawi
    Ernest Mazigo, Hojong Jun, Wang-Jong Lee, Johnsy Mary Louis, Jadidan Hada Syahada, Fadhila Fitriana, Fauzi Muh, Md Atique Ahmed, Feng Lu, Joon-Hee Han, Tae-Hyung Kwon, Se Jin Lee, Sunghun Na, Wanjoo Chun, Won Sun Park, Eun-Taek Han, Winifrida Kidima, Jin-
    Emerging Microbes & Infections.2025;[Epub]     CrossRef
  • First report of pfhrp2 and pfhrp3 gene deletions compromising HRP2-based malaria rapid diagnostic tests in Malawi
    Johnsy Mary Louis, Ernest Mazigo, Hojong Jun, Wang-Jong Lee, Jadidan Hada Syahada, Fadhila Fitriana, Fauzi Muh, Wanjoo Chun, Won Sun Park, Se Jin Lee, Sunghun Na, Feng Lu, Eun-Teak Han, Jin-Hee Han
    Infectious Diseases of Poverty.2025;[Epub]     CrossRef
  • Micro-geographic variation in antigenic diversity of PfEBA-175 region II in asymptomatic Plasmodium falciparum infections in Tanzania
    Jadidan Hada Syahada, Wang-Jong Lee, Hojong Jun, Johnsy Mary Louis, Fadhila Fitriana, Fauzi Muh, Feng Lu, Md Atique Ahmed, Sunghun Na, Wanjoo Chun, Won Sun Park, Bo-Young Jeon, Eun-Teak Han, Jim Todd, Alphaxard Manjurano, Winifrida Kidima, Ernest Mazigo,
    Frontiers in Immunology.2025;[Epub]     CrossRef
  • 3,622 View
  • 127 Download
  • 4 Web of Science
  • Crossref
Lophomonas blattarum-like organism in bronchoalveolar lavage from a pneumonia patient: current diagnostic scheme and polymerase chain reaction can lead to false-positive results
Moses Lee, Sang Mee Hwang, Jong Sun Park, Jae Hyeon Park, Jeong Su Park
Parasites Hosts Dis 2023;61(2):202-209.
Published online May 23, 2023
DOI: https://doi.org/10.3347/PHD.22107
Lophomonas blattarum is an anaerobic protozoan living in the intestine of cockroaches and house dust mites, with ultramicroscopic characteristics such as the presence of a parabasal body, axial filament, and absence of mitochondria. More than 200 cases of Lophomonas infection of the respiratory tract have been reported worldwide. However, the current diagnosis of such infection depends only on light microscopic morphological findings from respiratory secretions. In this study, we attempted to provide more robust evidence of protozoal infection in an immunocompromised patient with atypical pneumonia, positive for Lophomonas-like protozoal cell forms. A direct search of bronchoalveolar lavage fluid via polymerase chain reaction (PCR), transmission electron microscopy (TEM), and metagenomic next-generation sequencing did not prove the presence of protozoal infection. PCR results were not validated with sufficient rigor, while de novo assembly and taxonomic classification results did not confirm the presence of an unidentified pathogen. The TEM results implied that such protozoal forms in light microscopy are actually non-detached ciliated epithelial cells. After ruling out infectious causes, the patient’s final diagnosis was drug-induced pneumonitis. These findings underscore the lack of validation in the previously utilized diagnostic methods, and more evidence in the presence of L. blattarum is required to further prove its pathogenicity.

Citations

Citations to this article as recorded by  Crossref logo
  • Pulmonary infection by Lophomonas spp. and Aspergillus spp. in a B-cell acute lymphocytic leukemia patient from Chile
    Isabel Iturrieta-González, Enzo Moenen-Locoz, Alejandro Hidalgo, Fernando Vega, Johanna Cabrera, Carla Concha, Carolina Chahin, Javier Briones, Flery Fonseca-Salamanca
    Parasitology International.2025; 104: 102971.     CrossRef
  • A Reação em Cadeia da Polimerase (PCR) como estratégia de diagnóstico e monitoramento nas protozooses: uma revisão integrativa
    Luiza Valente Breda Libardi, Juliana Gouveia da Silva, Danieli Perini Alvares, Clara Fagundes Marely, Bruno Serafini Venturini, Guilherme Frinhani Bernardineli, Filipe Salume Lima Nogueira, Adelson Luiz Ferreira, Rodrigo Moraes, Priscila Pinto e Silva do
    Clinics Biopsychosocial.2025; 3(1): 58.     CrossRef
  • First Report of the Pulmonary Parasite Lophomonas blattarum in Ahvaz Province, Khuzestan: Case Report and Literature Review
    Mojtaba Aghaei, Hanieh Raji, Seyed Sobhan Bahreiny, Mohammad Amin Vahid, Najmaldin Saki
    Advanced Biomedical Research.2025;[Epub]     CrossRef
  • The diagnostic ambiguity for Polymerase Chain Reaction in the detection of Lophomonas blattarum
    Canan Doğu Tok, Funda Dogruman Al
    Middle Black Sea Journal of Health Science.2025; 11(4): 356.     CrossRef
  • First Molecular Evidence of Emerging Lophomonas Pathogen Among Patients Suspected of Having Pulmonary Tuberculosis in Mazandaran Province, Northern Iran
    Hossein Veisi, Abdollah Malakian, Mahdi Fakhar, Ali Sharifpour, Maryam Nakhaei, Mostafa Soleymani, Seyed Reza Mosave, Nader Ahangar, Seyed Hosien Seyedpour
    Acta Parasitologica.2024; 69(1): 1041.     CrossRef
  • Imaging patterns of Lophomonas blattarum infection in the respiratory tract: a registry-based analysis
    Amirmasoud Taheri, Mahdi Fakhar, Ali Sharifpour, Elhamsadat Banimostafavi, Sepideh SafaNavaei, Siavash Abedi, Hossein Mehravaran, Masoud Aliyali, Ahmad Shafahi, Asieh Delpzir
    BMC Infectious Diseases.2024;[Epub]     CrossRef
  • Case series of complicated bronchopulmonary lophomoniasis. Differential diagnosis of tuberculosis?
    Cristian Morán-Mariños, Juan Salas López, Felix Llanos-Tejada, Renato Casanova-Mendoza, Renzo Villanueva-Villegas, Antonella Chavez-Huamani, Kenneth G. Vargas-Ponce, Margaret Condori-Zevallos
    European Clinical Respiratory Journal.2024;[Epub]     CrossRef
  • Infliximab

    Reactions Weekly.2023; 1969(1): 197.     CrossRef
  • 4,323 View
  • 255 Download
  • 6 Web of Science
  • Crossref

Case Report

Imaging Manifestations and Misdiagnosis Analysis of Six Cases of Bone Hydatid Disease
Yanqiu Sun, Chunlong Yan, Dengfeng Tian, Chenhong Zhang, Qiang Zhang
Korean J Parasitol 2022;60(6):413-417.
Published online December 22, 2022
DOI: https://doi.org/10.3347/kjp.2022.60.6.413
We retrospectively evaluated the clinical and imaging features of 6 patients with bone hydatid disease confirmed by surgery and pathological examination. Among the 6 patients, 2 were infected with Echinococcosis granulosus metacestode and 4 were infected with E. multilocularis metacestode. The 2 cases with cystic echinococcosis were diagnosed by computed tomographic (CT) examination, and other 4 cases were diagnosed by magnetic resonance (MR) imaging. On the initial evaluation, 1 case each was misdiagnosed as a giant cell tumor or neurogenic tumor, and 2 were misdiagnosed as tuberculosis. The imaging manifestations of bone hydatid disease are complex, but most common findings include expansive osteolytic bone destruction, which may be associated with sclerosing edges or dead bone formation, localized soft tissue masses, and vertebral lesions with wedge-shaped changes and spinal stenosis. Combining imaging findings with the patient’s epidemiological history and immunological examinations is of great help in improving the diagnosis and differential diagnosis of bone hydatid disease.

Citations

Citations to this article as recorded by  Crossref logo
  • Spinal Echinococcosis in a Japanese Woman Living in Tokyo: Diagnostic Challenges in Non-endemic Areas and Public Health Implications
    Takashi Katsuno, Yuriko Sugiura, Momoko Morishita, Shuhei Osaki, Manabu Suzuki, Jin Takasaki, Motoyasu Iikura, Shinyu Izumi, Masayuki Hojo, Haruhito Sugiyama
    Internal Medicine.2025; 64(6): 971.     CrossRef
  • Dynamic evaluation of vertebral alveolar echinococcosis using MR T2 mapping
    Jinhuan Han, Yushan Chang, Hui Guo
    Journal of Orthopaedic Surgery.2025;[Epub]     CrossRef
  • Echinococcosis of the humerus with soft tissue and muscle involvement: A case report
    Weikai Chen, Yanan Zhang, Yin Wang, Gaosheng Yang
    Asian Journal of Surgery.2025; 48(6): 3870.     CrossRef
  • Pathological Fracture of the Tibia Due to Lytic Bone Lesion Caused by Hydatidosis with Absence of Systemic Involvement: A Case Report and Review of Literature
    Nashwah Samir AlHariry, Enas A. El Saftawy, Wesam Gamal Abousenna, Mansour A. Alghamdi, Basma Emad Aboulhoda
    Acta Parasitologica.2025;[Epub]     CrossRef
  • Current Perspectives on Cystic Echinococcosis: A Systematic Review
    Hawkar A. Nasralla, Berun A. Abdalla, Hiwa O. Abdullah, Sasan M. Ahmed, Fahmi H. Kakamad, Shvan H. Mohammed, Rawezh Q. Salih, Dahat A. Hussein, Tomas M. Mikael, Marwan N. Hassan, Hunar A. Hassan, Suhaib H. Kakamad, Kayhan A. Najar, Karukh K.
    Judi Clinical Journal.2025; 1(1): 12.     CrossRef
  • Mechanistic role of the IL-1β/c-Fos/NFATc1 signaling axis in echinococcal infection-promoted osteoclast differentiation and activation in pathological osteolysis: a prospective controlled trial
    Yelinaer Ayiheng, Wuluhan Mahan, Zengru Xie
    Journal of Orthopaedic Surgery and Research.2025;[Epub]     CrossRef
  • Complicated Hydatid Cyst Presentation: A Case Study on the Intersection of Cystobiliary Fistula, Bile Duct Obstruction, and Cholangitis: A Case Report
    Nasrin Razavianzadeh, Reza Dabiri, Aref Arminfar, Hessamedin Babaei, Faeze Gholipour, Farbod Noorbini, Soheil Shahramirad
    Clinical Case Reports.2025;[Epub]     CrossRef
  • Surgical Management of Cystic Pelvic Hydatid Bone Disease Using Additively Manufactured Customized Implants for Salvage Reconstruction: A Report of Two Cases
    Rodica Marinescu, Carmen Michaela Cretu, Stefan Ciumeica, Laptoiu Dan Constantin
    Cureus.2024;[Epub]     CrossRef
  • Hydatid cyst of the humerus presenting as a suspicious lesion: A rare case report and review of literature
    Chaymae Faraj, Khadija Laasri, Sara Essetti, Yahya El Harras, Nazik Allali, Siham El Haddad, Latifa Chat, Loubna Aqqaoui, Sarah Hosni, Fouad Ettayebi
    Radiology Case Reports.2024; 19(10): 4526.     CrossRef
  • Diagnostic Approach and Differences between Spinal Infections and Tumors
    Domenico Compagnone, Riccardo Cecchinato, Andrea Pezzi, Francesco Langella, Marco Damilano, Andrea Redaelli, Daniele Vanni, Claudio Lamartina, Pedro Berjano, Stefano Boriani
    Diagnostics.2023; 13(17): 2737.     CrossRef
  • Echinococcus granulosus promotes bone resorption by increasing osteoclasts differentiation
    Haohao Sun, Sibo Wang, Wenbo Tan, Ye Li, Qian Ren, Yaqing Liu, Yiping Huang, Chenhui Shi, Jing Li
    Acta Tropica.2023; 248: 107027.     CrossRef
  • 3,360 View
  • 110 Download
  • 8 Web of Science
  • Crossref

Original Articles

Characterization of a Peptide Antibody Specific to the Adenylyl Cyclase-Associated Protein of Acanthamoeba castellanii
Min-Jeong Kim, Hae-Ahm Lee, Fu-Shi Quan, Hyun-Hee Kong, Eun-Kyung Moon
Korean J Parasitol 2022;60(1):7-14.
Published online February 23, 2022
DOI: https://doi.org/10.3347/kjp.2022.60.1.7
Acanthamoeba keratitis (AK) is a rare infectious disease and accurate diagnosis has remained arduous as clinical manifestations of AK were similar to keratitis of viral, bacterial, or fungal origins. In this study, we described the production of a polyclonal peptide antibody against the adenylyl cyclase-associated protein (ACAP) of A. castellanii, and evaluated its differential diagnostic potential. Enzyme-linked immunosorbent assay revealed high titers of A. castellanii-specific IgG and IgA antibodies being present in low dilutions of immunized rabbit serum. Western blot analysis revealed that the ACAP antibody specifically interacted with A. castellanii, while not interacting with human corneal epithelial (HCE) cells and other causes of keratitis such as Fusarium solani, Pseudomonas aeruginosa, and Staphylococcus aureus. Immunocytochemistry (ICC) results confirmed the specific detection of trophozoites and cysts of A. castellanii co-cultured with HCE cells. The ACAP antibody also specifically interacted with the trophozoites and cysts of 5 other Acanthamoeba species. These results indicate that the ACAP antibody of A. castellanii can specifically detect multiple AK-causing members belonging to the genus Acanthamoeba and may be useful for differentially diagnosing Acanthamoeba infections.

Citations

Citations to this article as recorded by  Crossref logo
  • The pathogenesis, risk factors, diagnosis and treatment of Acanthamoeba keratitis
    Mingliang Bao, Hai Bao, Shuqing Wang, Hongyan Zhou
    Frontiers in Medicine.2025;[Epub]     CrossRef
  • A chorismate mutase-targeted, core-shell nanoassembly-activated SERS immunoassay platform for rapid non-invasive detection of Acanthamoeba infection
    Hyerin Lee, Min-Jeong Kim, Junkyu Chung, Wansun Kim, Hye-Jeong Jo, Tae Gi Kim, Jae-Ho Shin, Gi-Ja Lee, Fu-Shi Quan, Hyun-Hee Kong, Sang Woong Moon, Eun-Kyung Moon, Samjin Choi
    Nano Today.2024; 59: 102506.     CrossRef
  • Evaluating the Diagnostic Potential of Chorismate Mutase Poly-Clonal Peptide Antibody for the Acanthamoeba Keratitis in an Animal Model
    Min-Jeong Kim, Hye-Jeong Jo, Hae-Jin Sohn, Ho-Joon Shin, Fu-Shi Quan, Hyun-Hee Kong, Eun-Kyung Moon
    Pathogens.2023; 12(4): 526.     CrossRef
  • New Frontiers in Acanthamoeba Keratitis Diagnosis and Management
    Omar Shareef, Sana Shareef, Hajirah N. Saeed
    Biology.2023; 12(12): 1489.     CrossRef
  • Detection of Acanthamoeba from Acanthamoeba Keratitis Mouse Model Using Acanthamoeba-Specific Antibodies
    Min-Jeong Kim, A-Jeong Ham, A-Young Park, Hae-Jin Sohn, Ho-Joon Shin, Fu-Shi Quan, Hyun-Hee Kong, Eun-Kyung Moon
    Microorganisms.2022; 10(9): 1711.     CrossRef
  • 4,763 View
  • 179 Download
  • 5 Web of Science
  • Crossref
Echinococcus granulosus Protoscolex DM9 Protein Shows High Potential for Serodiagnosis of Alveolar Echinococcosis
Jeong-Geun Kim, Xiumin Han, Yoon Kong
Korean J Parasitol 2022;60(1):25-34.
Published online February 23, 2022
DOI: https://doi.org/10.3347/kjp.2022.60.1.25
Alveolar echinococcosis (AE) caused by infection with E. multilocularis metacestode, represents one of the most fatal helminthic diseases. AE is principally manifested with infiltrative, proliferating hepatic mass, resembling primary hepatocellular carcinoma. Sometimes metastatic lesions are found in nearby or remote tissue. AE diagnosis largely depends on imaging studies, but atypical findings of imaging features frequently require differential diagnosis from other hepatic lesions. Serological tests may provide further evidence, while obtaining reliable AE materials is not easy. In this study, alternative antigens, specific to AE were identified by analyzing E. granulosus protoscolex proteins. An immunoblot analysis of E. granulosus protoscolex showed that a group of low-molecular-weight proteins in the range from 14 kDa to 16 kDa exhibited a sensitive and specific immune response to AE patient sera. Partial purification and proteomic analysis indicated that this protein group contained myosin, tubulin polymerization promoting protein, fatty-acid binding protein, uncharacterized DM9, heat shock protein 90 cochaperone tebp P-23, and antigen S. When the serological applicability of recombinant forms of these proteins was assessed using enzyme-linked immunosorbent assay, DM9 protein (rEgDM9) showed 90.1% sensitivity (73/81 sera tested) and 94.5% specificity (172/181 sera tested), respectively. rEgDM9 showed weak cross-reactions with patient sera from the transitional and chronic stages of cystic echinococcosis (3 to 5 stages). rEgDM9 would serve as a useful alternative antigen for serodiagnosis of both early- and advanced-stage AE cases.
  • 4,620 View
  • 185 Download
Proteomic and Immunological Identification of Diagnostic Antigens from Spirometra erinaceieuropaei Plerocercoid
Yan Lu, Jia-Hui Sun, Li-Li Lu, Jia-Xu Chen, Peng Song, Lin Ai, Yu-Chun Cai, Lan-Hua Li, Shao-Hong Chen
Korean J Parasitol 2021;59(6):615-623.
Published online December 22, 2021
DOI: https://doi.org/10.3347/kjp.2021.59.6.615
Human sparganosis is a food-borne parasitic disease caused by the plerocercoids of Spirometra species. Clinical diagnosis of sparganosis is crucial for effective treatment, thus it is important to identify sensitive and specific antigens of plerocercoids. The aim of the current study was to identify and characterize the immunogenic proteins of Spirometra erinaceieuropaei plerocercoids that were recognized by patient sera. Crude soluble extract of the plerocercoids were separated using 2-dimensional gel electrophoresis coupled with immunoblot and mass spectrometry analysis. Based on immunoblotting patterns and mass spectrometry results, 8 antigenic proteins were identified from the plerocercoid. Among the proteins, cysteine protease protein might be developed as an antigen for diagnosis of sparganosis.

Citations

Citations to this article as recorded by  Crossref logo
  • Lysine acetylation in the spargana of Spirometra mansoni: Insights into glycolysis and EF-hand domain proteins
    Yuke Zeng, Asmaa M.I. Abuzeid, Qin Meng, Shuyu Chen, Xiaoruo Tan, Cuiqin Huang, Shiquan Lu, Teng Zhong, Yuanpeng Hu, Yisong Liu, Wei Liu
    Acta Tropica.2025; : 107932.     CrossRef
  • Establishment of Animal Infection Model of Spirometra Mansoni and Identification of Spirometra Mansoni by Enzyme-Linked Immunosorbent Assay
    Anqi Luo, Shuyu Chen, Mingye He, Xiaoruo Tan, Zhikang Li, Wei Liu, Yisong Liu
    Vector-Borne and Zoonotic Diseases.2024;[Epub]     CrossRef
  • Immunoproteomics: Approach to Diagnostic and Vaccine Development
    Virendra Supaji Gomase, Suchita Prabhakar Dhamane, Kiran Ramesh Kemkar, Pavan Ganpat Kakade, Abhay Dewappa Sakhare
    Protein & Peptide Letters.2024; 31(10): 773.     CrossRef
  • 4,385 View
  • 92 Download
  • 2 Web of Science
  • Crossref

Case Report

A Case of Human Hepatic Alveolar Echinococcosis Accompanied by Lung and Brain Metastases
Chuanchuan Liu, Haining Fan, Ri-li Ge
Korean J Parasitol 2021;59(3):291-296.
Published online June 21, 2021
DOI: https://doi.org/10.3347/kjp.2021.59.3.291
Alveolar echinococcosis (AE) is considered as a fatal zoonosis caused by the larvae of Echinococcus multilocularis. The lungs and brain are the most common metastatic organs. We report a human case of hepatic alveolar echinococcosis accompanied by lung and brain metastasis. In particular, the patient had a history of tuberculosis and the lung lesions were easily misdiagnosed as lung abscesses. The lesions of liver and lung underwent radical resection and confirmed as alveolar echinococcosis by pathological examination. The patient had no surgical complications after operation and was discharged after symptomatic treatment. Unfortunately, the patient later developed multiple intracerebral AE metastases. We required the patient to take albendazole orally for life and follow up.

Citations

Citations to this article as recorded by  Crossref logo
  • Alveolar Echinococcosis in 11-Month-Old Dog—Clinical Case
    Zuzana Šufliarska, Štefan Tóth, Michaela Gentil, Filip Humeník
    Pathogens.2025; 14(5): 450.     CrossRef
  • Surgical Approach in the Pulmonary Alveolar Echinococcus
    Yener Aydin, Ali Bilal Ulas, Nurhak Aksungur, Atilla Eroglu
    Archivos de Bronconeumología.2024; 60(6): 385.     CrossRef
  • Epididymal alveolar echinococcosis and tuberculosis co-infection: A case report
    Chuanchuan Liu, Hainin Fan
    IDCases.2024; 36: e01966.     CrossRef
  • Study on the mechanism of miRNAs on liver injury in the condition of Protoscocephalus alveolarus transhepatic portal vein infection
    Yazhou Zhu, Ming Li, Zihua Li, Jiahui Song, Wei Zhao
    Immunity, Inflammation and Disease.2024;[Epub]     CrossRef
  • Echinococcosis: An Uncommon Cause of Thoracic Pain
    Beatriz Sampaio, Felisbela Gomes, Mafalda Leal, Rita Bernardino
    Cureus.2024;[Epub]     CrossRef
  • Diagnosis and comparative analysis of surgical treatment of patients with liver alveococcosis
    V. S. Panteleev, M. A. Nartaylakov, I. Z. Salimgareev, A. S. Petrov
    Acta Biomedica Scientifica.2023; 8(2): 214.     CrossRef
  • A Surgically Resected Case of Multiple Pulmonary Metastases of Echinococcosis Presented with Bloody Phlegm
    Ryota NAGASHIMA, Yasushi CHO, Kenji WAKAYAMA, Shusaku TAKAHASHI, Hiroyuki ISHIZU, Shin ICHIHARA
    Nihon Rinsho Geka Gakkai Zasshi (Journal of Japan Surgical Association).2023; 84(9): 1442.     CrossRef
  • The Role of the Intestinal Epithelium in the “Weep and Sweep” Response during Gastro—Intestinal Helminth Infections
    Piotr Bąska, Luke James Norbury
    Animals.2022; 12(2): 175.     CrossRef
  • 4,878 View
  • 85 Download
  • 8 Web of Science
  • Crossref

Original Articles

Evaluation of Rapid IgG4 Test for Diagnosis of Gnathostomiasis
Yue Wang, An Ma, Xiao-Long Liu, Praphathip Eamsobhana, Xiao-Xian Gan
Korean J Parasitol 2021;59(3):257-263.
Published online June 21, 2021
DOI: https://doi.org/10.3347/kjp.2021.59.3.257
Human gnathostomiasis is a parasitic disease caused by Gnathostoma nematode infection. A rapid, reliable, and practical immunoassay, named dot immuno-gold filtration assay (DIGFA), was developed to supporting clinical diagnosis of gnathostomiasis. The practical tool detected anti-Gnathostoma-specific IgG4 in human serum using crude extract of third-stage larvae as antigen. The result of the test was shown by anti-human IgG4 monoclonal antibody conjugated colloidal gold. The sensitivity and specificity of the test were both 100% for detection in human sera from patients with gnathostomiasis (13/13) and from healthy negative controls (50/50), respectively. Cross-reactivity with heterogonous serum samples from patients with other helminthiases ranged from 0 (trichinosis, paragonimiasis, clonorchiasis, schistosomiasis, and cysticercosis) to 25.0% (sparganosis), with an average of 6.3% (7/112). Moreover, specific IgG4 antibodies diminished at 6 months after treatment. This study showed that DIGFA for the detection of specific IgG4 in human sera could be a promising tool for the diagnosis of gnathostomiasis and useful for evaluating therapeutic effects.

Citations

Citations to this article as recorded by  Crossref logo
  • Health Impact of Gnathostomiasis and its Integral Approach to Parasitic Infection: A Systematic Review
    Gisnella María Cedeño Cajas, José Andrés Zaporta Ramos, Andrea Stefannia Flores Villacrés, Cesar Guevara
    Salud, Ciencia y Tecnología.2024; 4: 1096.     CrossRef
  • 5,685 View
  • 118 Download
  • Crossref
Performance Evaluation of Biozentech Malaria Scanner in Plasmodium knowlesi and P. falciparum as a New Diagnostic Tool
Egy Rahman Firdaus, Ji-Hoon Park, Fauzi Muh, Seong-Kyun Lee, Jin-Hee Han, Chae-Seung Lim, Sung-Hun Na, Won Sun Park, Jeong-Hyun Park, Eun-Taek Han
Korean J Parasitol 2021;59(2):113-119.
Published online April 22, 2021
DOI: https://doi.org/10.3347/kjp.2021.59.2.113
The computer vision diagnostic approach currently generates several malaria diagnostic tools. It enhances the accessible and straightforward diagnostics that necessary for clinics and health centers in malaria-endemic areas. A new computer malaria diagnostics tool called the malaria scanner was used to investigate living malaria parasites with easy sample preparation, fast and user-friendly. The cultured Plasmodium parasites were used to confirm the sensitivity of this technique then compared to fluorescence-activated cell sorting (FACS) analysis and light microscopic examination. The measured percentage of parasitemia by the malaria scanner revealed higher precision than microscopy and was similar to FACS. The coefficients of variation of this technique were 1.2-6.7% for Plasmodium knowlesi and 0.3-4.8% for P. falciparum. It allowed determining parasitemia levels of 0.1% or higher, with coefficient of variation smaller than 10%. In terms of the precision range of parasitemia, both high and low ranges showed similar precision results. Pearson’s correlation test was used to evaluate the correlation data coming from all methods. A strong correlation of measured parasitemia (r2=0.99, P<0.05) was observed between each method. The parasitemia analysis using this new diagnostic tool needs technical improvement, particularly in the differentiation of malaria species.

Citations

Citations to this article as recorded by  Crossref logo
  • In-depth biological analysis of alteration in Plasmodium knowlesi-infected red blood cells using a noninvasive optical imaging technique
    Moh Egy Rahman Firdaus, Fauzi Muh, Ji-Hoon Park, Seong-Kyun Lee, Sung-Hun Na, Won-Sun Park, Kwon-Soo Ha, Jin-Hee Han, Eun-Taek Han
    Parasites & Vectors.2022;[Epub]     CrossRef
  • 5,870 View
  • 151 Download
  • 2 Web of Science
  • Crossref
Diagnostic Accuracy of Dermoscopy for Scabies
Feng-Zeng Li, Shuang Chen
Korean J Parasitol 2020;58(6):669-674.
Published online December 29, 2020
DOI: https://doi.org/10.3347/kjp.2020.58.6.669
The diagnostic accuracy of dermoscopy (DS) for scabies, a highly contagious parasitic disease, remains disputed. This study aimed to assess the diagnostic accuracy of DS in scabies, analyze the factors influencing DS, and explore its role in post-treatment evaluation. Patients with suspected scabies were randomly divided into 2 groups: 71 patients in the skin scraping (SS) group and 73 patients in the DS group. The diagnostic efficiencies of SS and DS in these groups were calculated. We also analyzed the influence of body part and investigator competence on the accuracy of DS. Then 16 body parts with typical signs of scabies were monitored by DS 2 and 4 day after sulfur ointment treatment. The sensitivity and specificity of DS were 98.3% and 88.5%, respectively. Hands, arms, and the abdomen had higher positivity rates than other body parts (P<0.001). The accuracy of dermatologists’ interpretations of images negative for scabies in the intermediate- and high-level groups was higher than that in the low-level group (P<0.001). At follow-up, the mites were still visible on 43.8% to 62.5% of the skin lesions 2 and 4 day after sulfur ointment treatment. These results showed that DS could significantly increase the accuracy of diagnosing scabies owing to its high sensitivity and specificity. Therefore, it may be useful for monitoring clinical responses to anti-parasitic treatment.

Citations

Citations to this article as recorded by  Crossref logo
  • Assessing the Accuracy of Dermoscopy for Scabies Diagnosis in Dark African Skin
    Nkechi Anne Enechukwu, Ikenna Akuakolam, Iloduba N Aghanya, Chetanna C Anaje, Ogochukwu I Ezejiofor, Enzo Errichetti
    Dermatology Practical & Conceptual.2025; 15(1): 4848.     CrossRef
  • Atypical Scabies Presenting as Annular Plaques: A Case Report and Review of the Literature
    Aimane Zaim, Hanane Baybay, Fatima Zahra Mernissi
    Cureus.2025;[Epub]     CrossRef
  • Dermoscopy-assisted localization of scabies mites on mineral oil preparations: a time-efficient diagnostic approach
    Kritin K. Verma, Helen Chen, Hannah Chaudhury, Denise C. Robson, Michelle B. Tarbox
    Baylor University Medical Center Proceedings.2025; 38(4): 582.     CrossRef
  • Scabies and other ectoparasitoses
    Cristina Galván-Casas, Carmen Salavastru, Juan Ortiz-Álvarez
    Clinical and Experimental Dermatology.2025;[Epub]     CrossRef
  • Identification of scabies by handheld microscopy
    Yat Fung Shea
    Oxford Medical Case Reports.2025;[Epub]     CrossRef
  • Rising scabies incidence in Spain: a retrospective observational analysis of four national data sources, 2011 to 2023
    Allegra Chatterjee, Álvaro Roy, Cristina García-Blázquez , Israel Cruz, Diana Gómez-Barroso, Miguel Ángel Descalzo, Rosario Planelló, Zaida Herrador
    Eurosurveillance.2025;[Epub]     CrossRef
  • Clinical Diagnosis and Dermatological Clues in Scabies
    Yasin Özdemir, Nağme Özdemir, İlteriş Oğuz Topal
    European Archives of Medical Research.2024; 40(1): 1.     CrossRef
  • Clinical practice guidelines for the diagnosis and treatment of scabies in Korea: Part 1. Epidemiology, clinical manifestations, and diagnosis — a secondary publication
    Jin Park, Soon-Hyo Kwon, Young Bok Lee, Hei Sung Kim, Jie Hyun Jeon, Gwang Seong Choi
    The Ewha Medical Journal.2024;[Epub]     CrossRef
  • Using ultraviolet dermoscopy in diagnosing scabies
    Aslan Yürekli, İlayda Muslu, Suzan Demir Pektaş, Emine Tuğba Alataş, Ceyda Tetik Aydoğdu, Dilek Daşgin
    Experimental Dermatology.2023; 32(11): 1996.     CrossRef
  • Scabies: Clinical Signs, Diagnosis and Current Treatment
    Huriye Aybüke KOÇ, Sezin ÜNLÜ AÇIKEL
    Archives of Current Medical Research.2023; 4(2): 62.     CrossRef
  • Dermoscopy of skin parasitoses, bites and stings: a systematic review of the literature
    P. Chauhan, R. Jindal, E. Errichetti
    Journal of the European Academy of Dermatology and Venereology.2022; 36(10): 1722.     CrossRef
  • Common pediatric infestations: update on diagnosis and treatment of scabies, head lice, and bed bugs
    Nonye Ogbuefi, Brandi Kenner-Bell
    Current Opinion in Pediatrics.2021; 33(4): 410.     CrossRef
  • Bedside Diagnostic Techniques in Dermatology
    Michael Goldenberg, Yi-Tin Liao, Karissa Libson, Stephanie Adame, Natalie Spaccarelli, Abraham Korman, Benjamin Kaffenberger, John C. L. Trinidad
    Current Dermatology Reports.2021; 10(3): 89.     CrossRef
  • Scabies: epidemiology, diagnosis, and treatment
    Cord Sunderkötter, Johannes Wohlrab, Henning Hamm
    Deutsches Ärzteblatt international.2021;[Epub]     CrossRef
  • 7,768 View
  • 169 Download
  • 13 Web of Science
  • Crossref
Morphological and Molecular Diagnosis of Necator americanus and Ancylostoma ceylanicum Recovered from Villagers in Northern Cambodia
Taehee Chang, Bong-Kwang Jung, Woon-Mok Sohn, Sooji Hong, Hyejoo Shin, Seungwan Ryoo, Jeonggyu Lee, Keon Hoon Lee, Virak Khieu, Rekol Huy, Jong-Yil Chai
Korean J Parasitol 2020;58(6):619-625.
Published online December 29, 2020
DOI: https://doi.org/10.3347/kjp.2020.58.6.619
Human hookworm infections caused by adult Ancylostoma spp. and Necator americanus are one of the most important tropical diseases. We performed a survey of intestinal helminths using the Kato-Katz fecal examination technique targeting 1,156 villagers residing in 2 northern provinces (Preah Vihear and Stung Treng) of Cambodia in 2018. The results revealed a high overall egg positive rate of intestinal helminths (61.9%), and the egg positive rate of hookworms was 11.6%. Nine of the hookworm egg positive cases in Preah Vihear Province were treated with 5-10 mg/kg pyrantel pamoate followed by purging with magnesium salts, and a total of 65 adult hookworms were expelled in diarrheic stools. The adult hookworms were analyzed morphologically and molecularly to confirm the species. The morphologies of the buccal cavity and dorsal rays on the costa were observed with a light microscope, and the nucleotide sequences of mitochondrial cytochrome c oxidase subunit 1 (cox1) gene were analyzed. The majority of the hookworm adults (90.7%) were N. americanus, whereas the remaining 9.3% were Ancylostoma ceylanicum, a rare hookworm species infecting humans. The results revealed a high prevalence of hookworm infections among people in a northern part of Cambodia, suggesting the necessity of a sustained survey combined with control measures against hookworm infections.

Citations

Citations to this article as recorded by  Crossref logo
  • The occurrence of cross-host species soil-transmitted helminth infections in humans and domestic/livestock animals: A systematic review
    Uniqueky Gratis Mawrie, Riviarynthia Kharkongor, María Martínez Valladares, Stella Kepha, Sitara S. R. Ajjampur, Rajiv Sarkar, Rachel Pullan, Muhammad Asaduzzaman
    PLOS Global Public Health.2025; 5(8): e0004614.     CrossRef
  • Hookworm infections in carnivores in Iran: a One Health concern
    Meysam Sharifdini, Aida Vafae Eslahi, Majid Pirestani, Ali Asghari, Giovanni Sgroi, Elham Hajialilo, Arian Ghannadi Karimi, Anastasia Diakou, Milad Badri
    BMC Veterinary Research.2025;[Epub]     CrossRef
  • Integrated Eco-Health approach significantly reduces helminth infections in endemic Khong islands with emphasis on Schistosoma mekongi
    Somphou Sayasone, Youthanavanh Vonghachack, Shang Xia, Shan Lv, Xiao-Nong Zhou, Peter Odermatt
    Infectious Diseases of Poverty.2024;[Epub]     CrossRef
  • Prevention of Ancylostomiasis Transmission in Livestock and Stockmen with Good Hygiene Behavior and Cage Sanitation
    Meiningtiyas Indriyanti, Sayono Sayono, Wahyu Handoyo, Tri Dewi Kristini, Didik Sumanto
    International Journal of Medical Parasitology and Epidemiology Sciences.2024; 5(1): 11.     CrossRef
  • High endemicity of Opisthorchis viverrini infection among people in northern Cambodia confirmed by adult worm expulsion
    Bong-Kwang Jung, Sooji Hong, Taehee Chang, Jaeeun Cho, Seungwan Ryoo, Keon Hoon Lee, Jeonggyu Lee, Woon-Mok Sohn, Sung-Jong Hong, Virak Khieu, Rekol Huy, Jong-Yil Chai
    Scientific Reports.2023;[Epub]     CrossRef
  • Hookworm infection in central China: morphological and molecular diagnosis
    Fang Fang Xu, Yu Fei Niu, Wen Qing Chen, Sha Sha Liu, Jing Ru Li, Peng Jiang, Zhong Quan Wang, Jing Cui, Xi Zhang
    Parasites & Vectors.2021;[Epub]     CrossRef
  • 8,418 View
  • 216 Download
  • 5 Web of Science
  • Crossref
Surveillance on the Vivax Malaria in Endemic Areas in the Republic of Korea Based on Molecular and Serological Analyses
Seong-Kyun Lee, Fengyue Hu, Egy Rahman Firdaus, Ji-Hoon Park, Jin-Hee Han, Sang-Eun Lee, Hyun-Il Shin, Shin Hyeong Cho, Won Sun Park, Feng Lu, Eun-Taek Han
Korean J Parasitol 2020;58(6):609-617.
Published online December 29, 2020
DOI: https://doi.org/10.3347/kjp.2020.58.6.609
Plasmodium vivax reemerged in 1993. It has been sustained for more than 25 years and become one of the important indigenous parasitic diseases in northern and western parts of the Republic of Korea near the demilitarized zone. In particular, relapse is a significant concern for the control of malaria, as short- and long-term incubation periods vary among those infected in Korea. In this study, the prevalence of asymptomatic carriers was examined among residents of high endemic areas of vivax malaria during nonseasonal transmission of mosquitoes. Blood samples from 3 endemic regions in northwestern Korea were evaluated by microscopic examination, rapid diagnostic testing, and nested PCR to identify asymptomatic patients carrying malaria parasites in the community. However, no positive malaria case among residents of endemic areas was detected. Additionally, serological analysis was carried out to measure antibodies against 3 antigenic recombinant proteins of P. vivax, merozoite surface protein 1-19, circumsporozoite surface protein-VK210, and liver-stage antigen (PvLSA-N), by the protein array method. Interestingly, seropositivity of sera between previous exposure and samples without exposure to malaria was significantly higher using the PvLSA-N antigen than the other antigens, suggesting that PvLSA-N can be used as a serological marker to analyze the degree of exposure for malaria transmission in endemic areas. This indicates a very low asymptomatic carrier prevalence during the nonmalaria season in the endemic areas of Korea.

Citations

Citations to this article as recorded by  Crossref logo
  • A region-structured model for early warning of Plasmodium vivax malaria transmission risk in the Republic of Korea
    Boyeon Kim, Jung Ho Kim, Jeehyun Lee, Joon-Sup Yeom
    Journal of Infection and Public Health.2025; 18(3): 102665.     CrossRef
  • Development of a Plasmodium vivax malaria model for evaluating the effects of control strategies on the malaria burden in Democratic People’s Republic of Korea
    Hye Seong, Jiyeon Suh, Jun Yong Choi, Jeehyun Lee, Joon-Sup Yeom
    Frontiers in Public Health.2024;[Epub]     CrossRef
  • Using Serological Markers for the Surveillance of Plasmodium vivax Malaria: A Scoping Review
    Lejla Kartal, Ivo Mueller, Rhea J. Longley
    Pathogens.2023; 12(6): 791.     CrossRef
  • Recent Spatial and Temporal Trends of Malaria in Korea
    Yeong Hoon Kim, Hye-Jin Ahn, Dongjae Kim, Sung-Jong Hong, Tong-Soo Kim, Ho-Woo Nam
    The Korean Journal of Parasitology.2021; 59(6): 585.     CrossRef
  • 5,393 View
  • 134 Download
  • 4 Web of Science
  • Crossref

Brief Communications

Evaluation of Rhophilin Associated Tail Protein (ROPN1L) in the Human Liver Fluke Opisthorchis viverrini for Diagnostic Approach
Amornrat Geadkaew-Krenc, Rudi Grams, Wansika Phadungsil, Wanlapa Chaibangyang, Nanthawat Kosa, Poom Adisakwattana, Paron Dekumyoy
Korean J Parasitol 2020;58(4):475-479.
Published online August 25, 2020
DOI: https://doi.org/10.3347/kjp.2020.58.4.475
Tegumental and excretory-secretory proteins are reported as diagnostic antigens for human opisthorchiasis. Rhophilin associated tail protein1-like (OvROPN1L) protein of Opisthorchis viverrini sperm tail showed potential as a diagnostic antigen. The OvROPN1L recombinant fragments were assayed for diagnostic antigenicity for human opisthorchiasis using indirect ELISA. The strongest antigenic region was a N-terminus peptide of M1 - P56. One synthetic peptide (P1, L3-Q13) of this region showed the highest antigenicity to opisthorchiasis. Sera from other parasitic infections including Strongyloides stercoralis, hookworm, Taenia spp, minute intestinal flukes, Paragonimus spp showed lower reactivity to P1. Peptide P1 is located in the disordered N-terminus of ROPN1L supporting its suitability as linear epitope. In the Platyhelminthes the N-terminal sequence of ROPN1L is diverging with taxonomic distance further suggesting that peptide P1 has potential as diagnostic tool in the genus Opisthorchis/Clonorchis. It should be further evaluated in combination with peptides derived from other O. viverrini antigens to increase its diagnostic power.

Citations

Citations to this article as recorded by  Crossref logo
  • Production and immunological characterization of the novel single-chain variable fragment (scFv) antibodies against the epitopes on Opisthorchis viverrini cathepsin F (OvCatF)
    Pongsakorn Martviset, Jeeraphong Thanongsaksrikul, Amornrat Geadkaew-Krenc, Salisa Chaimon, Kantaphon Glab-ampai, Wanlapa Chaibangyang, Phornphan Sornchuer, Potjanee Srimanote, Jittiporn Ruangtong, Parisa Prathaphan, Tonkla Taechadamrongtham, Nattaya Toru
    Acta Tropica.2024; 254: 107199.     CrossRef
  • Investigation of a Serine Protease Inhibitor Active in the Infectious Stage of the Human Liver Fluke Opisthorchis viverrini
    Rosnanee Salang, Wansika Phadungsil, Amornrat Geadkaew-Krenc, Rudi Grams
    Pathogens.2024; 13(8): 678.     CrossRef
  • Production and Immunological Characterization of scFv Specific to Epitope of Opisthorchis viverrini Rhophilin-Associated Tail Protein 1-like (OvROPN1L)
    Amornrat Geadkaew-Krenc, Dawid Krenc, Jeeraphong Thanongsaksrikul, Rudi Grams, Wansika Phadungsil, Kittirat Glab-ampai, Pathanin Chantree, Pongsakorn Martviset
    Tropical Medicine and Infectious Disease.2023; 8(3): 160.     CrossRef
  • Cystatins from the Human Liver Fluke Opisthorchis viverrini: Molecular Characterization and Functional Analysis
    Amornrat Geadkaew-Krenc, Rudi Grams, Sinee Siricoon, Nanthawat Kosa, Dawid Krenc, Wansika Phadungsil, Pongsakorn Martviset
    Pathogens.2023; 12(7): 949.     CrossRef
  • Novel recombinant proteins and peptides from Clonorchis sinensis and Opisthorchis viverrini for liver fluke exposure ELISA
    Sumathy Mohan, Mohan Natarajan, John G. Bruno
    Biochemistry and Biophysics Reports.2023; 35: 101516.     CrossRef
  • Screening of sperm antigen epitopes by phage display technique and its preliminary clinical application
    Jin-Chun Lu, Yan-Mei Ge, Yuan-Hua Xu, Shan-Shan Tang, Yuan-Jiao Liang
    Basic and Clinical Andrology.2022;[Epub]     CrossRef
  • 4,825 View
  • 93 Download
  • 6 Web of Science
  • Crossref
Molecular Diagnosis of Taenia saginata Tapeworms from Two Residents of Northern Cambodia
Taehee Chang, Bong-Kwang Jung, Woon-Mok Sohn, Sooji Hong, Hyejoo Shin, Seungwan Ryoo, Jeonggyu Lee, Keon Hoon Lee, Virak Khieu, Rekol Huy, Jong-Yil Chai
Korean J Parasitol 2020;58(2):201-204.
Published online April 30, 2020
DOI: https://doi.org/10.3347/kjp.2020.58.2.201
Taenia saginata infection has seldom been reported in Cambodia. In this study, we performed a survey of intestinal parasites in 1,156 residents of Preah Vihear and Stung Treng Provinces in 2018. The results revealed that 26 (2.4%) cases were positive for Taenia spp. eggs. In order to obtain the strobilae of the tapeworms, 2 patients in Preah Vihear were treated with praziquantel and purged with magnesium salts. The proglottids expelled after the medication were morphologically and molecularly analyzed to determine the species. The main uterine lateral braches in gravid proglottids were >15 in number suggesting that they are either T. saginata or Taenia asiatica. The sequences of the mitochondrial cytochrome c oxidase subunit 1 (cox1) gene and 2 nuclear loci, elongation factor-1 alpha (ef1) and ezrin-radixin-moesin-like protein (elp), were identical to the sequences of T. saginata available in GenBank but distant from Taenia solium, T. asiatica, and T. saginata-T. asiatica hybrid. This is the first report of the presence of T. saginata in the northern part of Cambodia bordering Lao PDR based on a molecular confirmation.

Citations

Citations to this article as recorded by  Crossref logo
  • High endemicity of Opisthorchis viverrini infection among people in northern Cambodia confirmed by adult worm expulsion
    Bong-Kwang Jung, Sooji Hong, Taehee Chang, Jaeeun Cho, Seungwan Ryoo, Keon Hoon Lee, Jeonggyu Lee, Woon-Mok Sohn, Sung-Jong Hong, Virak Khieu, Rekol Huy, Jong-Yil Chai
    Scientific Reports.2023;[Epub]     CrossRef
  • Occurrence of a Hybrid Between Taenia saginata and Taenia asiatica Tapeworms in Cambodia
    Taehee Chang, Bong-Kwang Jung, Sooji Hong, Hyejoo Shin, Seungwan Ryoo, Jeonggyu Lee, Keon Hoon Lee, Hansol Park, Keeseon S. Eom, Virak Khieu, Rekol Huy, Woon-Mok Sohn, Jong-Yil Chai
    The Korean Journal of Parasitology.2021; 59(2): 179.     CrossRef
  • Morphological and Molecular Diagnosis of Necator americanus and Ancylostoma ceylanicum Recovered from Villagers in Northern Cambodia
    Taehee Chang, Bong-Kwang Jung, Woon-Mok Sohn, Sooji Hong, Hyejoo Shin, Seungwan Ryoo, Jeonggyu Lee, Keon Hoon Lee, Virak Khieu, Rekol Huy, Jong-Yil Chai
    The Korean Journal of Parasitology.2020; 58(6): 619.     CrossRef
  • 7,757 View
  • 155 Download
  • 6 Web of Science
  • Crossref

Original Articles

Dientamoeba fragilis Infection in Patients with Digestive and Non-Digestive Symptoms: A Case-Control Study
Yousry A. Hawash, Khadiga A. Ismail, Taisir Saber, Emad M. Eed, Amany S. Khalifa, Khalaf F. Alsharif, Saleh A. Alghamdi
Korean J Parasitol 2020;58(2):129-134.
Published online April 30, 2020
DOI: https://doi.org/10.3347/kjp.2020.58.2.129
In most developing countries, Dientamoeba fragilis infection is an obscure protozoan infection. We aimed to determine a frequency and clinical importance of D. fragilis infection in Taif, Saudi Arabia. A 1-year case control study included patients with gastrointestinal (cases, n=114) or non-gastrointestinal symptoms (controls, n=90). The fecal samples were examined with the classical parasitological methods for intestinal protozoa, and by real time PCR for D. fragilis. The infection by D. fragilis was detected in 5.8% by PCR and in 4.4% patients by microscopy. The infection was identified more in control group (n=9) than in cases (n=3); a sole infection in 11 patients and mixed with Giardia in 1 patient. The other enteric parasites detected were Blastocystis sp. (8.3%), Giardia sp. (5.3%), Cryptosporidium sp. (2.9%), Entamoeba histolytica (1.4%), Entamoeba coli (0.9%) and Hymenolepis nana (0.4%). Our results tend to reinforce the need to increase awareness of D. fragilis infection in Saudi Arabia.

Citations

Citations to this article as recorded by  Crossref logo
  • Traitement des parasitoses intestinales (amœbose exclue)
    C. Prieux-Klotz, M.-C. Sabate Ferris, L. Gan, X. Bohand, P. Rey
    EMC - Gastro-entérologie.2024; 41(2): 1.     CrossRef
  • The high co-existence rate of Blastocystis and Dientamoeba fragilis in human faecal samples and the analysis of demographic and clinical findings
    Erdogan MALATYALİ, İbrahim YILDIZ, Evren TİLEKLİOGLU, Hatice ERTABAKLAR, Sema ERTUĞ
    Journal of Health Sciences and Medicine.2021; 4(4): 422.     CrossRef
  • The Coexistence of Blastocystis spp. in Humans, Animals and Environmental Sources from 2010–2021 in Asia
    Adedolapo Aminat Rauff-Adedotun, Farah Haziqah Meor Termizi, Nurshafarina Shaari, Ii Li Lee
    Biology.2021; 10(10): 990.     CrossRef
  • 10,566 View
  • 169 Download
  • 2 Web of Science
  • Crossref
Seroprevalence of Sarcocystis falcatula in Two Islands of Malaysia using Recombinant Surface Antigen 4
Tengku-Idris Tengku Idzzan Nadzirah, Fong Mun Yik, Lau Yee Ling
Korean J Parasitol 2020;58(1):1-5.
Published online February 29, 2020
DOI: https://doi.org/10.3347/kjp.2020.58.1.1
Sarcocystosis was diagnosed worldwide by serodiagnostic tests utilising the whole parasite, for which the protozoa were maintained in vitro are more costly. In this study, antigenicity of Sarcocystis falcatula recombinant protein (rSfSAG4) was investigated towards the local communities of Pangkor and Tioman Islands and its seroprevalence was surveyed in these islands. A total of 348 human sera were tested using rSfSAG4 by Western blot and ELISA. High prevalence of sarcocystosis was observed in Tioman Island (80.6%) than in Pangkor Island (50.0%) by Western blot. In ELISA, the seroprevalence observed in Tioman Island was 45.9%, whereas in Pangkor Island 63.0%. In other parasitic infections, the prevalence was 34.0% by Western blot and 46.0% by ELISA. In healthy control group, 7% by Western blot and 8% by ELISA showed positivity to rSfSAG4. It is suggested SfSAG4 is a candidate antigen to measure seroprevalence of sarcocystosis.

Citations

Citations to this article as recorded by  Crossref logo
  • Sarcocystis infection in domestic and wild avian hosts: Inseparable flight partners
    Petras Prakas, Rafael Calero-Bernal, Jitender P. Dubey
    Veterinary Parasitology.2025; 335: 110413.     CrossRef
  • 6,425 View
  • 176 Download
  • 1 Web of Science
  • Crossref
Malaria Prevalence in a Low Transmission Area, Jazan District of Southwestern Saudi Arabia
Yousry Hawash, Khadiga Ismail, Khalaf Alsharif, Walaa Alsanie
Korean J Parasitol 2019;57(3):233-242.
Published online June 30, 2019
DOI: https://doi.org/10.3347/kjp.2019.57.3.233
Detailed description of malaria in low transmission areas is crucial for elimination. The current study aimed to provide a comprehensive description for malaria transmission in Jazan, a low transmission district, southwestern Saudi Arabia. Patients at a tertiary care hospital were recruited in our study between August 2016 and September 2018. Malaria diagnosis was performed through a species-specific nested polymerase chain reaction (nested PCR), microscopy and Paramax-3TM rapid detection test (RDT). Malaria was detected in 30 patients by the PCR, with point prevalence of 10.9%. Of these malaria infections, 80% was imported, 26.6% was asymptomatic and 23.3% was sub-microscopic. Malaria was reported throughout the year, with February/March and September/October peaks. Infection was significantly more in males than in females (P=0.01). Likewise, infections were detected more in febrile than in non-febrile patients (P=0.01). Adult aged 15-24 years, fever and travel were identified as high-risk factors. Malaria was primarily attributed to Plasmodium falciparum mono-infections, followed by P. vivax mono-infections and lastly to falciparum/vivax mixed infections accounting 76.6%, 16.6%, and 6.6% of PCR-confirmed malaria cases, respectively. The nested PCR was superior to the smear microscopy (sensitivity 76.6%; specificity 100%) and the RDT (sensitivity 83.3%, specificity 94.2%). The overall percent agreement between microscopy and the RDT was 92.7% (kappa=0.63). High proportion of imported malaria including sub-microscopic and sub-patent cases were described. We suggest that incorporation of molecular tool into the conventional malaria diagnosis is beneficial in Jazan district.

Citations

Citations to this article as recorded by  Crossref logo
  • A study on the prevalence of the malaria parasite in the city of Sebha among expatriate workers from neighboring countries.
    Naima I. Al-Haddad , Rugaia M. Elsalem
    Libyan Journal of Science &Technology.2025; 15(1): 186.     CrossRef
  • Evaluation of Two Multiplexed qPCR Assays for Malaria Detection and Speciation: A Comparative Study With Nested PCR and Microscopy
    Ahmed A. Muyidi, Musa A. Ayashi, Majed H. Wakid, Maimonah S. Alghanmi, Fadi M. Baakdah, Hattan S. Gattan, Isra M. Alsaady, Muslimah N. Alsulami, Haleema H. Albohiri, Sarah A. Altwaim, Zaki M. Eisa, Thamer M. Brek, José F. Silveira
    Journal of Parasitology Research.2025;[Epub]     CrossRef
  • Asymptomatic/submicroscopic Plasmodium vivax infection: A systematic review and META-analysis on the hidden challenge for preventing re-establishment of malaria transmission
    Siqi Wang, He Yan, Li Zhang, Zhigui Xia, Jianhai Yin
    Parasite Epidemiology and Control.2025; 30: e00442.     CrossRef
  • The burden, clinical outcomes and risk factors related to neglected tropical diseases and malaria in migrant populations in the Middle East and North Africa: a systematic review and meta-analyses
    Eman Elafef, Taha Maatoug, Stella Evangelidou, Helena Marti-Soler, Asad Adam, Ahmed Hamed Arisha, Mahmoud Hilali, Sally Hargreaves, Ibrahim Bani, Farah Seedat, Ana Requena-Méndez
    BMJ Global Health.2025; 10(11): e019713.     CrossRef
  • Spatiotemporal Distribution of Malaria in the Kingdom of Saudi Arabia
    Ahmed Elagali, Mosa Shubayr, Elsiddig Noureldin, Kefyalew Addis Alene, Asmaa Elagali
    Tropical Medicine and Infectious Disease.2024; 9(1): 16.     CrossRef
  • Detection of Duffy blood group genotypes and submicroscopic Plasmodium infections using molecular diagnostic assays in febrile malaria patients
    Beka R. Abagero, Rei Rama, Abdulghani Obeid, Tirusew Tolosa, Biniyam Lukas, Taye Teka, Daniel Tesfaye, Eugenia Lo, Delenasaw Yewhalaw
    Malaria Journal.2024;[Epub]     CrossRef
  • Status of Malaria Infection in Saudi Arabia
    Amani Alhejely, V. Trukhachev, A. Skuratov, A. Shitikova, R. Migunov, R.Z. Abbas
    BIO Web of Conferences.2024; 139: 06036.     CrossRef
  • Machine learning models for predicting residual malaria infections using environmental factors: A case study of the Jazan region, Kingdom of Saudi Arabia
    Idris Zubairu Sadiq, Yakubu Saddeeq Abubakar, Abdulkadir Rabiu Salisu, Babangida Sanusi Katsayal, Umar Saidu, Sani I. Abba, Abdullahi Garba Usman
    Decoding Infection and Transmission.2024; 2: 100022.     CrossRef
  • Investigation of Wright Blood Group Alleles and Genotypes in Malaria-Endemic Area in Southwestern Saudi Arabia
    Amr Halawani, Saif Abdalla, Mahmoud Habibullah, Ghalia Shamlan, Neil Avent
    International Journal of General Medicine.2024; Volume 17: 5175.     CrossRef
  • Knowledge, attitudes, and practices (KAP) during the malaria elimination phase: A household-based cross-sectional survey
    Siddig Ibrahim Abdelwahab, Ibrahim M. Elhassan, Osama Albasheer, Manal Mohamed Elhassan Taha, Nasir Ahmed Ali, Yahya Salem Al-Jabiri, Waleed Madkhali, Ahmad A. Sahly, Bassem Oraibi, Ahmed Abdallah Ahmed Altraifi, Nasser Hakami, Mohammed M. Alshehri, Moham
    Medicine.2023; 102(22): e33793.     CrossRef
  • Association between interleukin-27 gene polymorphisms and Plasmodium falciparum Malaria
    Nada H. Aljarba, Mashael R. Al-Anazi, Tahani M. Al-Hazani, Mohammed I. Shafeai, Fuad H. Rudiny, Ali M. Motaen, Saad M. Bin Dajem, Hani Alothaid, Jahad Alghamdi, Saad Alkahtani, Ahmed A. Al-Qahtani
    Innate Immunity.2023; 29(5): 83.     CrossRef
  • Prevalence and proportion estimate of asymptomatic Plasmodium infection in Asia: a systematic review and meta-analysis
    Manas Kotepui, Kwuntida Uthaisar Kotepui, Frederick Ramirez Masangkay, Aongart Mahittikorn, Polrat Wilairatana
    Scientific Reports.2023;[Epub]     CrossRef
  • A decade of travel-associated malaria at King Fahad Hospital of the University in the Eastern Province of Saudi Arabia
    Ashwaq Alanazi, Bayan Ahmad Hasan Almusailhi, Gheed K. Bamousa, Nabaa H. Alhawashim, Nourah M. Alotaibi, Sumiyah AlShamekh, Basavaraja Channabasappa Hunasemarada, Reem Y. Al Jindan, Ayman A. El-Badry
    Scientific Reports.2022;[Epub]     CrossRef
  • Malarial Epidemiology among Patients in Al-Medina Al-Munawara, KSA
    Shady Mohammad Raji Al-Hussayni , Sami Oudah Eid Al-Harbi , Omar Hassan Amer
    International Journal of Life Science and Pharma Research.2022;[Epub]     CrossRef
  • Comparison of Rapid Diagnostic Test, Microscopy, and Polymerase Chain Reaction for the Detection of Plasmodium falciparum Malaria in a Low-Transmission Area, Jazan Region, Southwestern Saudi Arabia
    Aymen M. Madkhali, Ahmad Hassn Ghzwani, Hesham M. Al-Mekhlafi
    Diagnostics.2022; 12(6): 1485.     CrossRef
  • Genetic Diversity and Population Genetic Analysis of Plasmodium falciparum Thrombospondin Related Anonymous Protein (TRAP) in Clinical Samples from Saudi Arabia
    Saad M. Bin Dajem, Md Atique Ahmed, Fatimah F. Alghnnam, Shouq F. Alghannam, Gauspasha Yusuf Deshmukh, Rehan Haider Zaidi, Marie Fe F. Bohol, Syeda Sabiha Salam, Syeda Wasfeea Wazid, Mohammed I. Shafeai, Fuad H. Rudiny, Ali M. Motaen, Kareem Morsy, Ahmed
    Genes.2022; 13(7): 1149.     CrossRef
  • Low density Plasmodium infections and G6PD deficiency among malaria suspected febrile individuals in Ethiopia
    Beka R. Abagero, Daniel Kepple, Kareen Pestana, Logan Witherspoon, Abdissa Biruksew, Abinet Adanew, Fetiya Baharu, Shantoy Hansel, Karen Lopez, Daniel A. Janies, Eugenia Lo, Delenasaw Yewhalaw
    Frontiers in Tropical Diseases.2022;[Epub]     CrossRef
  • Current Status and the Epidemiology of Malaria in the Middle East Region and Beyond
    Mohammad Al-Awadhi, Suhail Ahmad, Jamshaid Iqbal
    Microorganisms.2021; 9(2): 338.     CrossRef
  • Malaria Rapid Diagnostic Tests: Literary Review and Recommendation for a Quality Assurance, Quality Control Algorithm
    Michael J. Kavanaugh, Steven E. Azzam, David M. Rockabrand
    Diagnostics.2021; 11(5): 768.     CrossRef
  • Current Epidemiological Characteristics of Imported Malaria, Vector Control Status and Malaria Elimination Prospects in the Gulf Cooperation Council (GCC) Countries
    Jamshaid Iqbal, Suhail Ahmad, Ali Sher, Mohammad Al-Awadhi
    Microorganisms.2021; 9(7): 1431.     CrossRef
  • Residual malaria in Jazan region, southwestern Saudi Arabia: the situation, challenges and climatic drivers of autochthonous malaria
    Hesham M. Al-Mekhlafi, Aymen M. Madkhali, Khalid Y. Ghailan, Ahmed A. Abdulhaq, Ahmad Hassn Ghzwani, Khalid Ammash Zain, Wahib M. Atroosh, Alkhansa Alshabi, Hussein A. Khadashi, Majid A. Darraj, Zaki M. Eisa
    Malaria Journal.2021;[Epub]     CrossRef
  • Case Report: Case report: Mixed infection of Plasmodium vivax and Plasmodium falciparum in a tertiary hospital
    Abeer M. Al-Subaie
    F1000Research.2021; 10: 779.     CrossRef
  • The global burden of Plasmodium vivax malaria is obscure and insidious
    Katherine E. Battle, J. Kevin Baird, Lorenz von Seidlein
    PLOS Medicine.2021; 18(10): e1003799.     CrossRef
  • The Distribution of Malaria with Seasonal in Kokap Yogyakarta 2012-2017
    Raden A.K. Lestari, Novyan Lusiyana, Fitria S. Nurochmah, G. Gholib, A. Sutriana, A. Engelhardt, J. Duboscq, R. Sahara Zamzami
    E3S Web of Conferences.2020; 151: 01018.     CrossRef
  • Systematic analysis of disease‐specific immunological signatures in patients with febrile illness from Saudi Arabia
    Yiu‐Wing Kam, Mohamed Yousif Ahmed, Siti Naqiah Amrun, Bernett Lee, Tarik Refaie, Kamla Elgizouli, Siew‐Wai Fong, Laurent Renia, Lisa FP Ng
    Clinical & Translational Immunology.2020;[Epub]     CrossRef
  • Rapid diagnostic tests forPlasmodium vivaxmalaria in endemic countries
    Ridhi Agarwal, Leslie Choi, Samuel Johnson, Yemisi Takwoingi
    Cochrane Database of Systematic Reviews.2020;[Epub]     CrossRef
  • Decreasing trend of imported malaria cases but increasing influx of mixed P. falciparum and P. vivax infections in malaria-free Kuwait
    Jamshaid Iqbal, Mohammad Al-Awadhi, Suhail Ahmad, Luzia Helena Carvalho
    PLOS ONE.2020; 15(12): e0243617.     CrossRef
  • Preparedness against self-infection and importation of Malaria - An airport survey among Saudis traveling to endemic countries
    HaninSaleh AlOwaini, RizwanSuliankatchi Abdulkader, QusayFahad Almahmoud, AbdulazizEyad Alqudaimi, RaneemSaied Al-Ghamdi, WateenAhmed Alhamoud, Hasan Keriri
    Journal of Family Medicine and Primary Care.2019; 8(10): 3318.     CrossRef
  • 10,278 View
  • 171 Download
  • 23 Web of Science
  • Crossref

Brief Communication

Differential Diagnosis of Human Sparganosis Using Multiplex PCR
Hyeong-Kyu Jeon, Kyu-Heon Kim, Woon-Mok Sohn, Keeseon S. Eom
Korean J Parasitol 2018;56(3):295-300.
Published online June 30, 2018
DOI: https://doi.org/10.3347/kjp.2018.56.3.295
Human sparganosis was diagnosed by morphological and genetic analyses in Korea. The complete mitochondrial genomes of Spirometra erinaceieuropaei and S. decipiens isolated in Korea have been recorded. Present study was performed to provide information to diagnose the etiologic agent of sparganosis by multiplex PCR using mitochondrial genome sequences of S. erinaceieuropaei and S. decipiens. In an effort to examine the differential diagnosis of spirometrid tapeworms, multiplex PCR assays were performed on plerocercoid larvae of S. erinaceieuropaei and S. decipiens. The PCR products obtained using species-specific primers were positively detected in all PCR assays on mixture of S. erinaceieuropaei and S. decipiens DNA. S. erinaceieuropaei-specific bands (239 bp and 401 bp) were obtained from all PCR assays using a mixture of S. erinaceieuropaei-specific primers (Se/Sd-1800F and Se-2018R; Se/Sd-7955F and Se-8356R) and S. erinaceieuropaei template DNA. S. decipiens-specific bands (540 bp and 644 bp) were also detected in all PCR assays containing mixtures of S. decipiens-specific primers (Se/Sd-1800F and Sd-2317R; Se/Sd-7955F and Sd-8567R) and S. decipiens template DNA. Sequence analyses on these species-specific bands revealed 100% sequence identity with homologous regions of the mtDNA sequences of S. erinaceieuropaei and S. decipiens. The multiplex PCR assay was useful for differential diagnosis of human sparganosis by detecting different sizes in species-specific bands.

Citations

Citations to this article as recorded by  Crossref logo
  • Molecular, morphological and histopathological evidence of Spirometra mansoni in wild and domestic animals from Costa Rica
    Irene Alvarado-Hidalgo, Josué Campos-Camacho, Yuliana Arguedas-Morales, Luis M. Romero-Vega, Alejandro Alfaro-Alarcón, Gabriela Anchia-Ureña, Laura G. Bass, Ivan Berrocal-Ávila, Isabel Hagnauer, Roberto W.I. Olivares, Alberto Solano-Barquero, Rodolfo Trau
    Veterinary Parasitology: Regional Studies and Reports.2024; 51: 101030.     CrossRef
  • Epidemiology, Diagnosis, and Prevention of Sparganosis in Asia
    Wei Liu, Tengfang Gong, Shuyu Chen, Quan Liu, Haoying Zhou, Junlin He, Yong Wu, Fen Li, Yisong Liu
    Animals.2022; 12(12): 1578.     CrossRef
  • Genetic and Morphological Identification of Spirometra decipiens in Snakes and Domestic Dog Found in Cuba
    Alexander Morales, Rebeca M. Laird-Pérez, Virginia Capó, Enrique Iglesias, Luis Fonte, Arturo Plascencia-Hernández, Enrique J. Calderón, Keeseon S. Eom, Yaxsier de Armas, Héctor R. Pérez-Gómez
    Pathogens.2022; 11(12): 1468.     CrossRef
  • An annotated checklist of the eukaryotic parasites of humans, exclusive of fungi and algae
    Blaine A. Mathison, Sarah G. H. Sapp
    ZooKeys.2021; 1069: 1.     CrossRef
  • Large-scale survey of a neglected agent of sparganosis Spirometra erinaceieuropaei (Cestoda: Diphyllobothriidae) in wild frogs in China
    Xi Zhang, Xiu Hong, Shi Nan Liu, Peng Jiang, Shu Chuan Zhao, Chuan Xi Sun, Zhong Quan Wang, Jing Cui, David Blair
    PLOS Neglected Tropical Diseases.2020; 14(2): e0008019.     CrossRef
  • African Lions and Zoonotic Diseases: Implications for Commercial Lion Farms in South Africa
    Jennah Green, Catherine Jakins, Eyob Asfaw, Nicholas Bruschi, Abbie Parker, Louise de Waal, Neil D’Cruze
    Animals.2020; 10(9): 1692.     CrossRef
  • 7,600 View
  • 135 Download
  • 7 Web of Science
  • Crossref

Original Article

Diagnosis, Treatment and Clinical Features of Cutaneous Leishmaniasis in Saudi Arabia
Yousry A. Hawash, Khadiga A. Ismail, Maha M. Abdel-Wahab, Mahmoud Khalifa
Korean J Parasitol 2018;56(3):229-236.
Published online June 30, 2018
DOI: https://doi.org/10.3347/kjp.2018.56.3.229
Cutaneous leishmaniasis (CL) has been one of the most common parasitic diseases in Saudi Arabia. This study exhibits the clinical features, diagnosis, cytokine profile and treatment of CL patients in Al-Taif province. Ninety CL suspects at a tertiary care general hospital were enrolled in one-year study. Patients were interviewed, clinically-examined, and subjected to laboratory tests: skin scraping smear microscopy, OligoC-TesT commercial PCR (Coris BioConcept) and kinetoplast DNA (kDNA) PCR for Leishmania diagnosis. Interferon-gamma (RayBio; Human IFN-γ) and nitric oxide (NO) levels in patients’ sera were evaluated before treatment with sodium stibogluconate (pentostam) with 20-day intramuscular drug regimen. Positive rates of microscopy, commercial PCR and kDNA PCR were 74.4%, 95.5% and 100%, respectively. Patients came to hospital mostly in winter (45.0%). CL was frequently exhibited in Saudi patients (78.8%), male gender (70.7%), age <20 years (50.0%), rural-dwellers (75.5%) and patients with travel history (86.6%). Lesion was mostly single ulcer (93.3%), occurred in the face (67.7%). Upon pentostam treatment, 85.1% of ulcers showed rapid healing signs. Levels of IFN-γ and NO were significantly higher in the healing than the non-healing cases (P<0.001). The kDNA PCR proved more sensitive than microscopy and OligoC-TesT commercial PCR. Our results open perspectives for IFN-γ use as a biomarker predicting treatment response.

Citations

Citations to this article as recorded by  Crossref logo
  • Neglected Tropical Diseases (NTDs) in Saudi Arabia: Systematic Review and Meta-analysis
    Najm Z. Alshahrani, Abdullah M. Alarifi, Abdullah M. Assiri
    Journal of Epidemiology and Global Health.2025;[Epub]     CrossRef
  • Tracking of Leishmania spp. in Iranian phlebotominae, distribution and biodiversity in Jarqavieh county, central Iran
    Mehdi Haddadnia, Mahsa Esmaeilifallah, Parisima Badiezadeh, Seyed Mohammad Abtahi
    International Journal of Environmental Health Research.2025; 35(12): 3761.     CrossRef
  • Epidemiology and clinical features of cutaneous leishmaniasis in Khyber Pakhtunkhwa, Pakistan
    W. Iqbal, U. Iram, S. Nisar, N. Musa, A. Alam, M. R. Khan, B. Ullah, M. Ullah, I. Ali
    Brazilian Journal of Biology.2024;[Epub]     CrossRef
  • Evaluation of the biodiversity and distribution of sand flies and tracking of Leishmania major in them in central Iran
    Parisima Badiezadeh, Mahsa Esmaeilifallah, Mehdi Haddadniaa, Seyed Mohammad Abtahi
    International Journal of Environmental Health Research.2024; 34(9): 3245.     CrossRef
  • Epidemiology and clinical features of parasitic disease Leishmaniasis. A case study from Pakistan
    Muhaibullah khan, Sheraz Ahmad, Hamayun saeed, M. Junaid Akhtar, Amna Munir
    Medical Reports.2024; 6: 100090.     CrossRef
  • Epidemiological Mapping of Cutaneous Leishmaniasis in Saudi Arabia: An Observational Descriptive Study
    Basmah Alharbi, Mawahib Ahmed
    Journal of Epidemiology and Global Health.2024; 14(3): 1281.     CrossRef
  • Dermoscopic features in relation to the type of clinical lesions in cutaneous leishmaniasis
    Qasim S. Al Chalabi, Hala N. Al Salman, Anfal L. Al harbawi
    Journal of the Egyptian Women's Dermatologic Society.2024; 21(3): 240.     CrossRef
  • Leishmaniasis: Recent epidemiological studies in the Middle East
    Chinyere A. Knight, David R. Harris, Shifaa O. Alshammari, Ayele Gugssa, Todd Young, Clarence M. Lee
    Frontiers in Microbiology.2023;[Epub]     CrossRef
  • Cutaneous Leishmaniasis: Associated Risk Factors and Prevention in Hubuna, Najran, Saudi Arabia
    Mohammed Jamaan Alzahrani, Nahid Elfaki, Yahya Hussein Ahmed Abdalla, Mugahed Ali Alkhadher, Maha Hamed Mohamed Ali, Waled AM Ahmed
    International Journal of General Medicine.2023; Volume 16: 723.     CrossRef
  • A disfiguring neglected tropical disease sweeps war-torn Yemen: a community-based study of prevalence and risk factors of cutaneous leishmaniasis among rural communities in the western highlands
    Manal A Al-Ashwal, Wahib M Atroosh, Abdulelah H Al-Adhroey, Assia A Al-Subbary, Lau Yee-Ling, Hesham M Al-Mekhlafi
    Transactions of The Royal Society of Tropical Medicine and Hygiene.2023; 117(12): 823.     CrossRef
  • Distribution, clinical features, and epidemiology of cutaneous leishmaniasis: A case study of District Haripur, KPK, Pakistan
    Muhaibullah Khan, Shehzad Ghayyur, Samina yasmin
    Medical Reports.2023; 2: 100025.     CrossRef
  • Cutaneous Leishmaniasis Prevalence and Clinical Overview: A Single Center Study from Saudi Arabia, Eastern Region, Al-Ahsa
    Mahdi Al-Dhafiri, Abdulmohsen Alhajri, Zahraa Ali Alwayel, Jasmine Ahmed Alturaiki, Shaima Ali Bu Izran, Fatimah Ahmed Alhammad, Ryhana Mohammed Aljumaiah
    Tropical Medicine and Infectious Disease.2023; 8(12): 507.     CrossRef
  • Distribution and epidemiological features of cutaneous leishmaniasis in Asir province, Saudi Arabia, from 2011 to 2020
    Yasser Alraey
    Journal of Infection and Public Health.2022; 15(7): 757.     CrossRef
  • Molecular characterization of Leishmania species from stray dogs and human patients in Saudi Arabia
    Abdullah D. Alanazi, Abdulazi S. Alouffi, Mohamed S. Alyousif, Abdulsadah A. Rahi, Magda A. Ali, Hend H. A. M. Abdullah, Fabio A. Brayner, Jairo Alfonso Mendoza-Roldan, Marcos Antonio Bezerra-Santos, Domenico Otranto
    Parasitology Research.2021; 120(12): 4241.     CrossRef
  • Clinical Diagnosis and Treatment Value of CT Three-Dimensional Imaging of Gynecological Pelvic Blood Vessels
    Li Qiao, Changxiao Li, Qinde Yu, Li Ma
    Journal of Medical Imaging and Health Informatics.2021; 11(6): 1743.     CrossRef
  • Prevalence of Leishmania species among patients with cutaneous leishmaniasis in Qassim province of Saudi Arabia
    Zafar Rasheed, Ahmed A. Ahmed, Tarek Salem, Mohammed S. Al-Dhubaibi, Ahmad A. Al Robaee, Abdullateef A. Alzolibani
    BMC Public Health.2019;[Epub]     CrossRef
  • 9,131 View
  • 152 Download
  • 15 Web of Science
  • Crossref

Brief Communication

Serodiagnosis of Extraintestinal Amebiasis: Retrospective Evaluation of the Diagnostic Performance of the Bordier® ELISA Kit
Nicolas Beyls, Odile Cognet, Jean-Paul Stahl, Olivier Rogeaux, Herve Pelloux
Korean J Parasitol 2018;56(1):71-74.
Published online February 28, 2018
DOI: https://doi.org/10.3347/kjp.2018.56.1.71
Soluble antigens from an axenic culture of Entamoeba histolytica were used to develop a commercial ELISA kit to quantify anti-E. histolytica antibodies in sera of patients with extraintestinal amebiasis in non-endemic settings. The diagnostic specificity and sensitivity of the test were assessed retrospectively using 131 human serum samples with amoebic serologic status available. They were selected according to their results in immunofluorescence (IFAT) and were separated in 2 sample categories: 64 sera with positive results by IFAT and 67 with negative results by IFAT. The sensitivity and specificity of the ELISA kit were assessed at 95.0% and 94.0% compared to the IFAT. The test can be useful to exclude a potential diagnosis of amebiasis and could be used as a screening method since ELISA is an automated technique.

Citations

Citations to this article as recorded by  Crossref logo
  • A proof-of-concept point-of-care test for the serodiagnosis of human amebic liver abscess
    Rutchanee Rodpai, Penchom Janwan, Lakkhana Sadaow, Patcharaporn Boonroumkaew, Oranuch Sanpool, Tongjit Thanchomnang, Hiroshi Yamasaki, Toshihiro Mita, Pewpan M. Intapan, Wanchai Maleewong
    PeerJ.2025; 13: e19181.     CrossRef
  • Serodiagnosis of amoebic abscess: a retrospective diagnostic accuracy study of kits marketed in Europe
    E. Prétot, M-P. Brenier-Pinchart, P. Tirard-Collet, F. Gabriel, F. Touafek, A. Marteau, L. Delcey, C. Amiot, D. Dupont, H. Fricker-Hidalgo, H. Sokol, A. Moreno-Sabater, F. Grenouillet, Bobbi S. Pritt
    Journal of Clinical Microbiology.2025;[Epub]     CrossRef
  • Unusual microscopic finding in a hepatic abscess content
    Marta Rolo, Alhena Reyes, Juan Martín Torres, Ana Pérez-Ayala
    Enfermedades Infecciosas y Microbiología Clínica.2023; 41(4): 254.     CrossRef
  • Unusual microscopic finding in a hepatic abscess content
    Marta Rolo, Alhena Reyes, Juan Martín Torres, Ana Pérez-Ayala
    Enfermedades infecciosas y microbiologia clinica (English ed.).2023; 41(4): 254.     CrossRef
  • Evaluation of total immunoglobulin G and subclass antibodies in an enzyme-linked immunosorbent assay for serodiagnosis of human amebic liver abscess
    Penchom Janwan, Lakkhana Sadaow, Rutchanee Rodpai, Hiroshi Yamasaki, Vor Luvira, Wattana Sukeepaisarnjaroen, Amnat Kitkhuandee, Krisada Paonariang, Oranuch Sanpool, Patcharaporn Boonroumkaew, Tongjit Thanchomnang, Toshihiro Mita, Pewpan M. Intapan, Wanch
    PeerJ.2022; 10: e14085.     CrossRef
  • Difficultés d’interprétation des sérologies parasitaires, hors toxoplasmose
    Sandrine Houzé, Luc Paris
    Revue Francophone des Laboratoires.2022; 2022(545): 40.     CrossRef
  • Multi-Laboratory Evaluation of a Lateral Flow Rapid Test for Detection of Amebic Liver Abscess
    Rahmah Noordin, Muhammad Hafiznur Yunus, Syazwan Saidin, Zeehaida Mohamed, Isabel Fuentes Corripio, José Miguel Rubio, Majid Golkar, Shamilah Hisam, Rogan Lee, Rohela Mahmud
    The American Journal of Tropical Medicine and Hygiene.2020; 103(6): 2233.     CrossRef
  • 9,037 View
  • 178 Download
  • 6 Web of Science
  • Crossref

Original Article

An Alternative Method for Extracting Plasmodium DNA from EDTA Whole Blood for Malaria Diagnosis
Krongkaew Seesui, Kanokwan Imtawil, Phimphakon Chanetmahun, Porntip Laummaunwai, Thidarut Boonmars
Korean J Parasitol 2018;56(1):25-32.
Published online February 28, 2018
DOI: https://doi.org/10.3347/kjp.2018.56.1.25
Molecular techniques have been introduced for malaria diagnosis because they offer greater sensitivity and specificity than microscopic examinations. Therefore, DNA isolation methods have been developed for easy preparation and cost effectiveness. The present study described a simple protocol for Plasmodium DNA isolation from EDTA-whole blood. This study demonstrated that after heating infected blood samples with Tris?EDTA buffer and proteinase K solution, without isolation and purification steps, the supernatant can be used as a DNA template for amplification by PCR. The sensitivity of the extracted DNA of Plasmodium falciparum and Plasmodium vivax was separately analyzed by both PCR and semi-nested PCR (Sn-PCR). The results revealed that for PCR the limit of detection was 40 parasites/μl for P. falciparum and 35.2 parasites/μl for P. vivax, whereas for Sn-PCR the limit of detection was 1.6 parasites/μl for P. falciparum and 1.4 parasites/μl for P. vivax. This new method was then verified by DNA extraction of whole blood from 11 asymptomatic Myanmar migrant workers and analyzed by Sn-PCR. The results revealed that DNA can be extracted from all samples, and there were 2 positive samples for Plasmodium (P. falciparum and P. vivax). Therefore, the protocol can be an alternative method for DNA extraction in laboratories with limited resources and a lack of trained technicians for malaria diagnosis. In addition, this protocol can be applied for subclinical cases, and this will be helpful for epidemiology and control.

Citations

Citations to this article as recorded by  Crossref logo
  • Evaluation of A Simple DNA Extraction Method and Its Combination with Loop-Mediated Isothermal Amplification Assays for Rapid Plasmodium knowlesi Diagnosis
    Meng-Yee Lai, Mohd Hafizi Abdul Hamid, Jenarun Jelip, Rose Nani Mudin, Yee-Ling Lau
    Tropical Medicine and Infectious Disease.2023; 8(8): 389.     CrossRef
  • Liquid Biopsy for Promising Non-invasive Diagnostic Biomarkers in Parasitic Infections
    Eylem Akdur Ozturk, Ayse Caner
    Acta Parasitologica.2022; 67(1): 1.     CrossRef
  • Comparison of six methods for Loa loa genomic DNA extraction
    Roland Dieki, Elsa-Rush Eyang-Assengone, Patrice Makouloutou-Nzassi, Félicien Bangueboussa, Edouard Nsi Emvo, Jean Paul Akue, Ricardo Santos
    PLOS ONE.2022; 17(3): e0265582.     CrossRef
  • Protein abundance and folding rather than the redox state of Kelch13 determine the artemisinin susceptibility of Plasmodium falciparum
    Robin Schumann, Eileen Bischoff, Severina Klaus, Sophie Möhring, Julia Flock, Sandro Keller, Kim Remans, Markus Ganter, Marcel Deponte
    Redox Biology.2021; 48: 102177.     CrossRef
  • 9,579 View
  • 228 Download
  • 6 Web of Science
  • Crossref

Case Report

Human Cases of Fascioliasis in Fujian Province, China
Lin Ai, Yu-Chun Cai, Yan Lu, Jia-Xu Chen, Shao-Hong Chen
Korean J Parasitol 2017;55(1):55-60.
Published online February 28, 2017
DOI: https://doi.org/10.3347/kjp.2017.55.1.55
Fascioliasis is a foodborne zoonotic parasitic disease. We report 4 cases occurring in the same family, in whom diagnosis of acute fascioliasis was established after series of tests. One case was hospitalized with fever, eosinophilia, and hepatic lesions. MRI showed hypodense changes in both liver lobes. The remaining 3 cases presented with the symptom of stomachache only. Stool analysis was positive for Fasciola eggs in 2 adult patients. The immunological test and molecular identification of eggs were confirmed at the National Institute of Parasitic Diseases, Chinese Center for Disease Control and Prevention, Shanghai, China. The results of serological detection were positive in all the 4 patients. DNA sequencing of PCR products of the eggs demonstrated 100% homology with ITS and cox1 of Fasciola hepatica. The conditions of the patients were not improved by broad-spectrum anti-parasitic drugs until administration of triclabendazole.

Citations

Citations to this article as recorded by  Crossref logo
  • Prevalence and associated risk factors assessment of bovine fasciolosis in the Imbo Region, Burundi
    Sylvère Nkurunziza, Gérard Nishemezwe, Jean-Bosco Ntirandekura, Pascal Niyokwizera, Lionel Nyabongo, Amos Omore, Rose Odhiambo
    Parasitology Research.2024;[Epub]     CrossRef
  • Phylogenetic Characteristics of Fasciola hepatica Isolated from a Korean Patient
    Mi Jin Jeong, Jae Kyun Park, Hak Sun Yu
    The Korean Journal of Parasitology.2022; 60(5): 367.     CrossRef
  • Letter to the editor discussing the article “curved tunnel’ sign on MRI: a typical radiological feature in hepatic trichinellosis”
    Jean Dupouy-Camet, Fabrizio Bruschi, Edoardo Pozio
    Abdominal Radiology.2021; 46(9): 4521.     CrossRef
  • Extracellular vesicles from Fasciola gigantica induce cellular response to stress of host cells
    Aijiang Guo, Li Wang, Xuelian Meng, Shaohua Zhang, Zhaoan Sheng, Xuenong Luo, Weiyi Huang, Shuai Wang, Xuepeng Cai
    Experimental Parasitology.2021; 231: 108173.     CrossRef
  • New insight into genetic variation and haplotype diversity of Fasciola hepatica from Algeria
    Linda Chougar, Nabil Amor, Sarra Farjallah, Khaled Harhoura, Miriem Aissi, Abdulaziz N. Alagaili, Paolo Merella
    Parasitology Research.2019; 118(4): 1179.     CrossRef
  • Prevalence and risk factors of Fascioliasis in China
    Lin Ai, Jia-Xu Chen, Yu-Chun Cai, Yan Lu, Yan-Hong Chu, Shao-Hong Chen, Hao Li, Peng Song, Mu-Xin Chen, Xiao-Nong Zhou
    Acta Tropica.2019; 196: 180.     CrossRef
  • Neglected tropical diseases in the People’s Republic of China: progress towards elimination
    Men-Bao Qian, Jin Chen, Robert Bergquist, Zhong-Jie Li, Shi-Zhu Li, Ning Xiao, Jürg Utzinger, Xiao-Nong Zhou
    Infectious Diseases of Poverty.2019;[Epub]     CrossRef
  • Recent developments in the epidemiology, diagnosis, and treatment of Fasciola infection
    Camille M. Webb, Miguel M. Cabada
    Current Opinion in Infectious Diseases.2018; 31(5): 409.     CrossRef
  • Dynamics of liver enzymes in rabbits experimentally infected with Fasciola sp. (Intermediate form from Japan)
    Wipaporn JARUJAREET, Kensuke TAIRA, Hong Kean OOI
    Journal of Veterinary Medical Science.2018; 80(1): 36.     CrossRef
  • 11,639 View
  • 223 Download
  • 10 Web of Science
  • Crossref

Brief Communications

Optimization of Trichomonas vaginalis Diagnosis during Pregnancy at a University Hospital, Argentina
Pamela Testardini, Mar?a Luc?a Gallo Vaulet, Andrea Carolina Entrocassi, Claudia Menghi, Martha Cora Eliseht, Claudia Gatta, Mirta Losada, Mar?a Sol Touz?n, Ana Corominas, Carlos Vay, Silvio Tatti, Angela Famiglietti, Marcelo Rodriguez Fermepin, Beatriz Perazzi
Korean J Parasitol 2016;54(2):191-195.
Published online April 30, 2016
DOI: https://doi.org/10.3347/kjp.2016.54.2.191
The aim of this study was to evaluate different methods for Trichomonas vaginalis diagnosis during pregnancy in order to prevent maternal and perinatal complications. A total of 386 vaginal exudates from pregnant women were analyzed. T. vaginalis was investigated by 3 types of microscopic examinations direct wet mount with physiologic saline solution, prolonged May-Grunwald Giemsa (MGG) staining, and wet mount with sodium-acetate-formalin (SAF)/methylene blue method. PCR for 18S rRNA gene as well as culture in liquid medium were performed. The sensitivity and specificity of the microscopic examinations were evaluated considering the culture media positivity or the PCR techniques as gold standard. The frequency of T. vaginalis infection was 6.2% by culture and/or PCR, 5.2% by PCR, 4.7% by culture, 3.1% by SAF/methylene blue method and 2.8% by direct wet smear and prolonged MGG staining. The sensitivities were 83.3%, 75.0%, 50.0%, and 45.8% for PCR, culture, SAF/methylene blue method, and direct wet smear-prolonged MGG staining, respectively. The specificity was 100% for all the assessed methods. Microscopic examinations showed low sensitivity, mainly in asymptomatic pregnant patients. It is necessary to improve the detection of T. vaginalis using combined methods providing higher sensitivity, such as culture and PCR, mainly in asymptomatic pregnant patients, in order to prevent maternal and perinatal complications.

Citations

Citations to this article as recorded by  Crossref logo
  • Diagnostic accuracy of real-time polymerase chain reaction assay for the detection of Trichomonas vaginalis in clinical samples: A systematic review and meta-analysis
    Emmanuel O. Babafemi, Benny P. Cherian, Khalid Rahman, Gilbert M. Mogoko, Oluwatoyin O. Abiola
    African Journal of Laboratory Medicine.2025;[Epub]     CrossRef
  • Prevalence and risk factors of Mycoplasma genitalium, Chlamydia trachomatis, Neisseria gonorrhoeae and Trichomonas vaginalis infections in pregnant women in seven hospitals in N’Djamena, Chad: a cro
    Mahamat Mustapha Anouar, Boris Emmanuel Djoumsie Gomseu, Nandita Sharma, Sana Afreen, Tenzin Tsephel, Djamal Hachim, Ngam Daita, Annour Bechir Ahmat, Mahamat Mouctar Abdelkerim, Aboubakar Hassan Adam, Adam Mahamat Dahabaye, Chatté Adawaye, Foumsou Lhagada
    BMJ Open.2025; 15(10): e096775.     CrossRef
  • Establishment of a programmatic detection method for Trichomonas vaginalis based on double antibody sandwich ELISA targeting TvCP39 antigen
    Yuhua Li, Fakun Li, Wenjie Tian, Yani Zhang, Weijuan Wang, Zhenke Yang, Xiaowei Tian, Shuai Wang, Xuefang Mei, Zhenchao Zhang
    Acta Tropica.2024; 260: 107489.     CrossRef
  • Construction a novel detection method for Trichomonas vaginalis based on recombinant enzyme polymerase amplification targeting the Actin gene
    Fakun Li, Yangyang Deng, Wanxin Sheng, Xihui Gao, Weijuan Wang, Zhili Chu, Xuefang Mei, Zhenke Yang, Xiaowei Tian, Shuai Wang, Zhenchao Zhang
    Journal of Eukaryotic Microbiology.2023;[Epub]     CrossRef
  • The International Society for the Study of Vulvovaginal Disease Vaginal Wet Mount Microscopy Guidelines: How to Perform, Applications, and Interpretation
    Pedro Vieira-Baptista, Švitrigailė Grincevičienė, Caroline Oliveira, José Fonseca-Moutinho, Facundo Cherey, Colleen Kennedy Stockdale
    Journal of Lower Genital Tract Disease.2021; 25(2): 172.     CrossRef
  • Development of a convenient detection method for Trichomonas vaginalis based on loop-mediated isothermal amplification targeting adhesion protein 65
    Yuhua Li, Shuai Wang, Haoran Li, Xiaoxiao Song, Hao Zhang, Yujuan Duan, Chengyang Luo, Bingli Wang, Sifan Ji, Qing Xie, Zhenchao Zhang
    BMC Infectious Diseases.2020;[Epub]     CrossRef
  • Análisis microbiológico del tracto genital materno y de la sangre del cordón umbilical en relación con el daño neonatal
    Silvina E. Cocucci, Mirtha G. Santacruz Silvero, Mirta O. Losada, María S. Touzón, Hilda RudaVega, Manuel Vazquez Blanco, Sergio L. Provenzano, Carlos A. Vay, Ángela M.R. Famiglietti, Beatriz E. Perazzi
    Revista Argentina de Microbiología.2019; 51(2): 157.     CrossRef
  • Chlamydia, gonorrhoea, trichomoniasis and syphilis: global prevalence and incidence estimates, 2016
    Jane Rowley, Stephen Vander Hoorn, Eline Korenromp, Nicola Low, Magnus Unemo, Laith J Abu-Raddad, R Matthew Chico, Alex Smolak, Lori Newman, Sami Gottlieb, Soe Soe Thwin, Nathalie Broutet, Melanie M Taylor
    Bulletin of the World Health Organization.2019; 97(8): 548.     CrossRef
  • Very low sensitivity of wet mount microscopy compared to PCR against culture in the diagnosis of vaginal trichomoniasis in Uganda: a cross sectional study
    Sheila Nabweyambo, Othman Kakaire, Stefanie Sowinski, Alfred Okeng, Henry Ojiambo, Joshua Kimeze, Irene Najjingo, Freddie Bwanga
    BMC Research Notes.2017;[Epub]     CrossRef
  • 9,845 View
  • 122 Download
  • 8 Web of Science
  • Crossref
Prevalence of Trichomonas vaginalis by PCR in Men Attending a Primary Care Urology Clinic in South Korea
Jun-Hyeok Seo, Hye-Won Yang, So-Young Joo, Su-Min Song, Yu-Ran Lee, Jae-Sook Ryu, Eun Sang Yoo, Won Kee Lee, Hyun-Hee Kong, Sang-Eun Lee, Won-Ja Lee, Youn-Kyoung Goo, Dong-Il Chung, Yeonchul Hong
Korean J Parasitol 2014;52(5):551-555.
Published online October 22, 2014
DOI: https://doi.org/10.3347/kjp.2014.52.5.551

Trichomonas vaginalis, a causative agent of trichomoniasis, may trigger symptomatic or asymptomatic nongonococcal urethritis and chronic prostatitis in men. Despite the availability of highly sensitive diagnostic tests, such as nucleic acid amplification tests, including PCR, few prospective studies present data on male T. vaginalis infection in South Korea. In the present study, the prevalence of T. vaginalis and associated clinical conditions were evaluated in 201 male patients from a primary care urology clinic in South Korea. The prevalence of T. vaginalis infection in our cohort was 4% (8/201) by PCR. T. vaginalis infection was common in men older than 40 years (median age, 52 years). Among the 8 Trichomonas-positive patients, 87.5% (7/8) had prostatic diseases, such as prostatitis and benign prostatic hyperplasia, and 25.0% (2/8) and 12.5% (1/8) were coinfected with Chlamydia trachomatis and Mycoplasma genitalium, respectively. Our results suggest that T. vaginalis infection is not rare in men attending primary care urology clinics in South Korea, especially in those older than 40 years, in whom it may explain the presence of prostatic disease. The possibility of T. vaginalis infection should be routinely considered in older male patients with prostatic diseases in South Korea.

Citations

Citations to this article as recorded by  Crossref logo
  • Trichomoniasis in Men: A Neglected Factor in Male Infertility?
    Seyed Ali Hosseini, Mohammad Matini, Maryam Bahmanzadeh, Reza Aslani, Faeze Foroughi-Parvar
    Acta Parasitologica.2025;[Epub]     CrossRef
  • Systematic review and meta-analysis of the global prevalence and infection risk factors of Trichomonas vaginalis
    Wenjie Tian, Yuhua Li, Yani Zhang, Yiming Zhang, Yiran Qin, Yalin Han, Dongxian Li, Shuai Wang, Zhenke Yang, Xiaowei Tian, Xuefang Mei, Zhenchao Zhang
    Parasite.2025; 32: 56.     CrossRef
  • Prevalence of trichomoniasis infection among adults in Nigerian community settings
    K. Chukwuemeka Obetta, Innocent Okonkwo Ogbonna, Dorida Nneka Oyigbo, Oliver Onyemaechi Ugwu, Kenneth Okonkwo Ugwu, Beatrice N. Onah, Chinasa Maryrose Ugwunnadi, Joseph O. Acha, Ngozi Uzoamaka Chuke, Ogechi Nkemjika, Onyinyechi Elizabeth Okoye
    Medicine.2023; 102(37): e34585.     CrossRef
  • Prevalence and Genotype of Trichomonas vaginalis among Men in Xinxiang City, Henan Province, China
    Zhenchao Zhang, Yuhui Sang, Pucheng Wu, Yujia Shang, Lesong Li, Yujuan Duan, Linfei Zhao, Minghui Gao, Lihua Guo, Xiaowei Tian, Zhenke Yang, Shuai Wang, Lixia Hao, Xuefang Mei, Jianbing Mu
    Journal of Tropical Medicine.2023; 2023: 1.     CrossRef
  • Inflammatory response to Trichomonas vaginalis in the pathogenesis of prostatitis and benign prostatic hyperplasia
    Ik-Hwan Han, Jung-Hyun Kim, Jae-Sook Ryu
    Parasites, Hosts and Diseases.2023; 61(1): 2.     CrossRef
  • Urogenital Trichomonas vaginalis infection in males: a case report and retrospective analysis of a 10‐year period in a tertiary hospital
    Miguel Alpalhão, Luís Marques‐Lito, Paulo Filipe, João Borges‐Costa
    International Journal of Dermatology.2022;[Epub]     CrossRef
  • Seroprevalence and risk factors of Trichomonas vaginalis among couples in Al-Hamza city-Iraq.
    Musafer H. Al-Ardi
    Al-Kufa University Journal for Biology.2021; 13(1): 26.     CrossRef
  • Comparison of Seropositivity to Trichomonas vaginalis between Men with Prostatic Tumor and Normal Men
    Jung-Hyun Kim, Hong-Sang Moon, Kyu-Shik Kim, Hwan-Sik Hwang, Jae-Sook Ryu, Sung-Yul Park
    The Korean Journal of Parasitology.2019; 57(1): 21.     CrossRef
  • Comparison of Two PCR Assays for Trichomonas vaginalis
    Chang-Suk Noh, Sang-Su Kim, Sung-Yul Park, Hong-Sang Moon, Yeonchul Hong, Jae-Sook Ryu
    The Korean Journal of Parasitology.2019; 57(1): 27.     CrossRef
  • Status of common parasitic diseases in Korea in 2019
    Sun Huh
    Journal of the Korean Medical Association.2019; 62(8): 437.     CrossRef
  • Prevalence of Trichomonas vaginalis in Women Visiting 2 Obstetrics and Gynecology Clinics in Daegu, South Korea
    Youn-Kyoung Goo, Won-Sik Shin, Hye-Won Yang, So-Young Joo, Su-Min Song, Jae-Sook Ryu, Won-Myung Lee, Hyun-Hee Kong, Won-Ki Lee, Sang-Eun Lee, Won-Ja Lee, Dong-Il Chung, Yeonchul Hong
    The Korean Journal of Parasitology.2016; 54(1): 75.     CrossRef
  • Prostatic Disease Associated withTrichomonas vaginalis
    Jae-Sook Ryu
    The Korean Journal of Urogenital Tract Infection and Inflammation.2014; 9(2): 61.     CrossRef
  • 11,534 View
  • 127 Download
  • 13 Web of Science
  • Crossref

Original Article

A New IgG Immunoblot Kit for Diagnosis of Toxoplasmosis in Pregnant Women
Imen Khammari, Fatma Saghrouni, Sami Lakhal, Aida Bouratbine, Moncef Ben Said, Jalel Boukadida
Korean J Parasitol 2014;52(5):493-499.
Published online October 22, 2014
DOI: https://doi.org/10.3347/kjp.2014.52.5.493

The determination of the accurate immune status of pregnant women is crucial in order to prevent congenital toxoplasmosis. Equivocal results with conventional serological techniques are not uncommon when IgG titers are close to the cut-off value of the test, so that a confirmatory technique is needed. For this purpose, we developed a homemade immunoblot (IB) using soluble extract of Toxoplasma gondii tachyzoites and assessed it by testing 154 positive, 100 negative, and 123 equivocal sera obtained from pregnant women. In order to select the more valuable bands in terms of sensitivity and specificity, we used the Youden Index (YI). The highest YIs were those given by the 32, 36, 98, 21, and 33 bands. The simultaneous presence on the same blot of at least 3 bands showed a much higher YI (0.964) and was adapted as the positivity criterion. The analysis of results showed that our homemade IB correlated well with the commercial LDBIO Toxo II IgG® kit recently recommended as a confirmatory test (96.7% of concordance).

Citations

Citations to this article as recorded by  Crossref logo
  • Systematic Review and Meta-Analysis of Congenital Toxoplasmosis Diagnosis: Advances and Challenges
    Priscila Silva Franco, Ana Carolina Morais Oliveira Scussel, Rafaela José Silva, Thadia Evelyn Araújo, Henrique Tomaz Gonzaga, Camila Ferreira Marcon, Joaquim Pedro Brito-de-Sousa, Angélica Lemos Debs Diniz, Marina Carvalho Paschoini, Bellisa Freitas Barb
    Journal of Tropical Medicine.2024; 2024: 1.     CrossRef
  • Trend in serological and molecular diagnostic methods for Toxoplasma gondii infection
    Min-ju Kim, Soeun J. Park, Hyunwoo Park
    European Journal of Medical Research.2024;[Epub]     CrossRef
  • Diagnostic Accuracy of LDBIO-Toxo II IgG and IgM Western Blot in Suspected Seroconversion in Pregnancy: A Multicentre Study
    Valeria Meroni, Francesca Genco, Luigia Scudeller, Marie-Pierre Brenier-Pinchart, Hélène Fricker-Hidalgo, Coralie L’Ollivier, Luc Paris, Hervé Pelloux
    Pathogens.2022; 11(6): 665.     CrossRef
  • Serological diagnosis of toxoplasmosis: evaluation of the commercial test recomLine Toxoplasma IgG immunoblot (Mikrogen) based on recombinant antigens
    Vincent Jean-Pierre, Julien Miozzo, Hélène Fricker-Hidalgo, Cécile Garnaud, Marie Gladys Robert, Hervé Pelloux, Marie-Pierre Brenier-Pinchart
    Parasite.2022; 29: 52.     CrossRef
  • A longitudinal study of Toxoplasma gondii seroconversion on four large Danish sow farms
    Abbey Olsen, Lis Alban, Matthew Denwood, Hans Houe, Tina Birk Jensen, Henrik Vedel Nielsen
    Veterinary Parasitology.2021; 295: 109460.     CrossRef
  • Performance of seven commercial automated assays for the detection of low levels of anti-Toxoplasma IgG in French immunocompromised patients
    Tiphaine Douet, Catherine Armengol, Elena Charpentier, Pamela Chauvin, Sophie Cassaing, Xavier Iriart, Antoine Berry, Judith Fillaux
    Parasite.2019; 26: 51.     CrossRef
  • Performance of Zika Assays in the Context of Toxoplasma gondii, Parvovirus B19, Rubella Virus, and Cytomegalovirus (TORCH) Diagnostic Assays
    Bettie Voordouw, Barry Rockx, Thomas Jaenisch, Pieter Fraaij, Philippe Mayaud, Ann Vossen, Marion Koopmans
    Clinical Microbiology Reviews.2019;[Epub]     CrossRef
  • Semiquantitative Dot Blot with the GRA8 antigen to differentiate the stages of toxoplasmosis infection
    Juan Gabriel Costa, María Julia Vilariño
    Journal of Microbiological Methods.2018; 149: 9.     CrossRef
  • Knowledge and Practices of Toxoplasmosis among Clinical Laboratory Professionals: A Cross-Sectional Study in Durango, Mexico
    Cosme Alvarado-Esquivel, Luis Sánchez-Anguiano, Luis Berumen-Segovia, Jesús Hernández-Tinoco, Yazmin Rico-Almochantaf, Alfredo Cisneros-Camacho, Jorge Cisneros-Martínez
    International Journal of Environmental Research and Public Health.2017; 14(11): 1413.     CrossRef
  • Sensing parasites: Proteomic and advanced bio-detection alternatives
    Carlos Sánchez-Ovejero, Fernando Benito-Lopez, Paula Díez, Adriano Casulli, Mar Siles-Lucas, Manuel Fuentes, Raúl Manzano-Román
    Journal of Proteomics.2016; 136: 145.     CrossRef
  • The impact of lowering the cut-off value on the sensitivity of the Platelia Elisa IgG (Bio-Rad) test for toxoplasmosis diagnosis
    Oussama Mouri, Eric Kendjo, Feriel Touafek, Arnaud Fekkar, Ousmane Konte, Sebastien Imbert, Régis Courtin, Dominique Mazier, Luc Paris
    Parasite.2015; 22: 22.     CrossRef
  • 10,028 View
  • 117 Download
  • 12 Web of Science
  • Crossref

Mini Review

New Molecules in Babesia gibsoni and Their Application for Diagnosis, Vaccine Development, and Drug Discovery
Youn-Kyoung Goo, Xuenan Xuan
Korean J Parasitol 2014;52(4):345-353.
Published online August 29, 2014
DOI: https://doi.org/10.3347/kjp.2014.52.4.345

Babesia gibsoni is an intraerythrocytic apicomplexan parasite that causes piroplasmosis in dogs. B. gibsoni infection is characterized clinically by fever, regenerative anemia, splenomegaly, and sometimes death. Since no vaccine is available, rapid and accurate diagnosis and prompt treatment of infected animals are required to control this disease. Over the past decade, several candidate molecules have been identified using biomolecular techniques in the authors' laboratory for the development of a serodiagnostic method, vaccine, and drug for B. gibsoni. This review article describes newly identified candidate molecules and their applications for diagnosis, vaccine production, and drug development of B. gibsoni.

Citations

Citations to this article as recorded by  Crossref logo
  • Standardization of quantitative PCR (qPCR) method to detect the level of parasitaemia in Babesia gibsoni infected dogs
    Varuna Purushothama Panicker, Athira Narayanan, Ajith Kumar Sreedharan Nair, Anjaly Krishnan, Nimna Ajay, Vinod Kumar
    Journal of Microbiological Methods.2024; 224: 107009.     CrossRef
  • Phylogenetic analysis of Babesia gibsoni isolates of south India using apical membrane antigen, 50 kDa surface antigen, and 70 kDa heat shock protein genes
    Chundayil Kalarickal Deepa, Anju Varghese, Christophe Angeline Felicia Bora, Karapparambu Gopalan Ajith Kumar, Lijo John, Muhasin Asaf, Sunanda Chulliparambil, Reghu Ravindran
    Experimental Parasitology.2023; 246: 108461.     CrossRef
  • Identification of three members of the multidomain adhesion CCp family in Babesia gibsoni
    Hang Li, Shengwei Ji, Eloiza May Galon, Iqra Zafar, Zhuowei Ma, Thom Do, Moaz M. Amer, Yihong Ma, Junya Yamagishi, Mingming Liu, Xuenan Xuan
    Acta Tropica.2023; 241: 106890.     CrossRef
  • Babesia gibsoni Whole-Genome Sequencing, Assembling, Annotation, and Comparative Analysis
    Qin Liu, Xing-Ai Guan, Dong-Fang Li, Ya-Xin Zheng, Sen Wang, Xue-Nan Xuan, Jun-Long Zhao, Lan He, Jian Li
    Microbiology Spectrum.2023;[Epub]     CrossRef
  • Evaluation of recombinant Babesia gibsoni thrombospondin-related adhesive protein (BgTRAP) for the sero-diagnosis of canine babesiosis
    Chundayil Kalarickal Deepa, Anju Varghese, Karapparambu Gopalan Ajith Kumar, Ashwathappa Nandini, Gatchanda Shravan Kumar, Prabodh Kumar Hembram, Chemmangattuvalappil Narendranath Dinesh, Sanis Juliet, Jess Vergis, Ollukkara Krishnan Sindhu, Reghu Ravindr
    Experimental Parasitology.2023; 254: 108621.     CrossRef
  • Babesia gibsoni
    Mingming Liu, Ikuo Igarashi, Xuenan Xuan
    Trends in Parasitology.2022; 38(9): 815.     CrossRef
  • Molecular survey and phylogenetic analysis of Babesia vogeli in dogs
    Abdelfattah Selim, Ameer Megahed, Mourad Ben Said, Abdullah D. Alanazi, Mohamed Z. Sayed-Ahmed
    Scientific Reports.2022;[Epub]     CrossRef
  • Establishment and Application of an Indirect Enzyme-Linked Immunosorbent Assay for Measuring GPI-Anchored Protein 52 (P52) Antibodies in Babesia gibsoni-Infected Dogs
    Qin Liu, Xueyan Zhan, Dongfang Li, Junlong Zhao, Haiyong Wei, Heba Alzan, Lan He
    Animals.2022; 12(9): 1197.     CrossRef
  • Evaluation of the Inhibitory Effects of Six Natural Product Extracts against Babesia gibsoni in Vitro and in Vivo
    Xiaohu Zhai, Lingxu Li, Peihao Zhang, Yiwen Guo, Huaide Jiang, Weihua He, Yanyan Li, Bin Zhang, Dawei Yao
    Journal of Parasitology.2022;[Epub]     CrossRef
  • In vitro screening of novel anti-Babesia gibsoni drugs from natural products
    Shengwei Ji, Mingming Liu, Eloiza May Galon, Mohamed Abdo Rizk, Jixu Li, Yongchang Li, Iqra Zafar, Ikuo Igarashi, Xuenan Xuan
    Parasitology International.2021; 85: 102437.     CrossRef
  • The Infection and Species Identification of Canine Babesia spp. in Parts of Shaanxi Province
    Wuren Ma, Huan Tang, Yu Zhou, Guanghui Zhao, Yunpeng Fan, Xiaoping Song, Junke Song
    Journal of Parasitology.2021;[Epub]     CrossRef
  • Closing the empty anti-Babesia gibsoni drug pipeline in vitro using fluorescence-based high throughput screening assay
    Mohamed Abdo Rizk, Shengwei Ji, Mingming Liu, Shimaa Abd El-Salam El-Sayed, Yongchang Li, Benedicto Byamukama, Aaron Edmond Ringo, Xuenan Xuan, Ikuo Igarashi
    Parasitology International.2020; 75: 102054.     CrossRef
  • Babesia canis spp. in dogs in Baghdad Province, Iraq: First molecular identification and clinical and epidemiological study
    Naseir Mohammed Badawi, Afaf Abdulrahman Yousif
    Veterinary World.2020; 13(3): 579.     CrossRef
  • Survey and Molecular Study of Babesia gibsoni in Dogs of Baghdad Province, Iraq
    Naseir M. Badawi, Afaf A. Yousif
    The Iraqi Journal of Veterinary Medicine.2020; 44((E0)): 34.     CrossRef
  • To kill a piroplasm: genetic technologies to advance drug discovery and target identification in Babesia
    Caroline D. Keroack, Brendan Elsworth, Manoj T. Duraisingh
    International Journal for Parasitology.2019; 49(2): 153.     CrossRef
  • Babesia gibsoni endemic to Wuhan, China: mitochondrial genome sequencing, annotation, and comparison with apicomplexan parasites
    Jiaying Guo, Xiaoyan Miao, Pei He, Muxiao Li, Sen Wang, Jie Cui, Cuiqin Huang, Lan He, Junlong Zhao
    Parasitology Research.2019; 118(1): 235.     CrossRef
  • Inhibitory effects of the phytohormone inhibitors fluridone and inabenfide against Babesia gibsoni in vitro
    Mingming Liu, Tatsunori Masatani, Paul Franck Adjou Moumouni, Seung-Hun Lee, Eloiza May Galon, Yang Gao, Huanping Guo, Jixu Li, Yongchang Li, Xuenan Xuan
    Veterinary Parasitology.2019; 265: 19.     CrossRef
  • Evaluation of Babesia gibsoni GPI-anchored Protein 47 (BgGPI47-WH) as a Potential Diagnostic Antigen by Enzyme-Linked Immunosorbent Assay
    Xueyan Zhan, Long Yu, Xiaomeng An, Qin Liu, Muxiao Li, Zheng Nie, Yangnan Zhao, Sen Wang, Yangsiqi Ao, Yu Tian, Lan He, Junlong Zhao
    Frontiers in Veterinary Science.2019;[Epub]     CrossRef
  • Identification and characterization of interchangeable cross-species functional promoters between Babesia gibsoni and Babesia bovis
    Mingming Liu, Paul Franck Adjou Moumouni, Shinuo Cao, Masahito Asada, Guanbo Wang, Yang Gao, Huanping Guo, Jixu Li, Patrick Vudriko, Artemis Efstratiou, Aaron Edmond Ringo, Seung-Hun Lee, Hassan Hakimi, Tatsunori Masatani, Fujiko Sunaga, Shin-ichiro Kawaz
    Ticks and Tick-borne Diseases.2018; 9(2): 330.     CrossRef
  • Establishment of a stable transfection system for genetic manipulation of Babesia gibsoni
    Mingming Liu, Paul Franck Adjou Moumouni, Masahito Asada, Hassan Hakimi, Tatsunori Masatani, Patrick Vudriko, Seung-Hun Lee, Shin-ichiro Kawazu, Junya Yamagishi, Xuenan Xuan
    Parasites & Vectors.2018;[Epub]     CrossRef
  • Two Imported Cases of Babesiosis with Complication or Co-Infection with Lyme Disease in Republic of Korea
    Hea Yoon Kwon, Jae Hyoung Im, Yun-Kyu Park, Areum Durey, Jin-Soo Lee, Ji Hyeon Baek
    The Korean Journal of Parasitology.2018; 56(6): 609.     CrossRef
  • Transient transfection of intraerythrocytic Babesia gibsoni using elongation factor-1 alpha promoter
    Mingming Liu, Masahito Asada, Shinuo Cao, Paul Franck Adjou Moumouni, Patrick Vudriko, Artemis Efstratiou, Hassan Hakimi, Tatsunori Masatani, Fujiko Sunaga, Shin-ichiro Kawazu, Junya Yamagishi, Xuenan Xuan
    Molecular and Biochemical Parasitology.2017; 216: 56.     CrossRef
  • 15,278 View
  • 143 Download
  • 23 Web of Science
  • Crossref

Case Reports

A Case of Fasciola hepatica Infection Mimicking Cholangiocarcinoma and ITS-1 Sequencing of the Worm
Bong Kyun Kang, Bong-Kwang Jung, Yoon Suk Lee, In Kyeom Hwang, Hyemi Lim, Jaeeun Cho, Jin-Hyeok Hwang, Jong-Yil Chai
Korean J Parasitol 2014;52(2):193-196.
Published online April 18, 2014
DOI: https://doi.org/10.3347/kjp.2014.52.2.193

Fascioliasis is a zoonotic infection caused by Fasciola hepatica or Fasciola gigantica. We report an 87-year-old Korean male patient with postprandial abdominal pain and discomfort due to F. hepatica infection who was diagnosed and managed by endoscopic retrograde cholangiopancreatography (ERCP) with extraction of 2 worms. At his first visit to the hospital, a gallbladder stone was suspected. CT and magnetic retrograde cholangiopancreatography (MRCP) showed an intraductal mass in the common bile duct (CBD) without proximal duct dilatation. Based on radiological findings, the presumed diagnosis was intraductal cholangiocarcinoma. However, in ERCP which was performed for biliary decompression and tissue diagnosis, movable materials were detected in the CBD. Using a basket, 2 living leaf-like parasites were removed. The worms were morphologically compatible with F. hepatica. To rule out the possibility of the worms to be another morphologically close species, in particular F. gigantica, 1 specimen was processed for genetic analysis of its ITS-1 region. The results showed that the present worms were genetically identical (100%) with F. hepatica but different from F. gigantica.

Citations

Citations to this article as recorded by  Crossref logo
  • A Curious Culprit Behind Biliary Pus: What’s the Diagnosis?
    Partha Pal, Uday Kumar Marri, D. Nageshwar Reddy
    Gastroenterology.2025;[Epub]     CrossRef
  • Parasitic Diseases of Upper Gastrointestinal Tract
    Heung Up Kim
    The Korean Journal of Helicobacter and Upper Gastrointestinal Research.2024; 24(2): 127.     CrossRef
  • Global distribution of zoonotic digenetic trematodes: a scoping review
    Yue Hu, Rong-Jian Zhan, Shi-Lin Lu, Yi-Yang Zhang, Min-Yu Zhou, Hui Huang, Ding-Ding Wang, Tao Zhang, Zi-Xin Huang, Yun-Fei Zhou, Zhi-Yue Lv
    Infectious Diseases of Poverty.2024;[Epub]     CrossRef
  • General overview of the current status of human foodborne trematodiasis
    Jong-Yil Chai, Bong-Kwang Jung
    Parasitology.2022; 149(10): 1262.     CrossRef
  • Phylogenetic Characteristics of Fasciola hepatica Isolated from a Korean Patient
    Mi Jin Jeong, Jae Kyun Park, Hak Sun Yu
    The Korean Journal of Parasitology.2022; 60(5): 367.     CrossRef
  • Fasciola Hepatica Induced Hepatic Abscess Treated with Triclabendazole
    Hyun Joon Park, Gil-Soon Choi, Minjung Jung, Sang Uk Lee
    The Korean Journal of Gastroenterology.2021; 77(1): 39.     CrossRef
  • Oxysterols of helminth parasites and pathogenesis of foodborne hepatic trematodiasis caused by Opisthorchis and Fasciola species
    Nuno Vale, Maria João Gouveia, Fátima Gärtner, Paul J Brindley
    Parasitology Research.2020; 119(5): 1443.     CrossRef
  • Prolonged antibiotic use leading to Clostridium difficile colitis in an ill returned traveller with acute fascioliasis
    Dylan Kain, Avinash N Mukkala, Andrea K Boggild
    Journal of Travel Medicine.2018;[Epub]     CrossRef
  • A Case of Fascioliasis in A Wild Nutria, Myocastor coypus, in Republic of Korea
    Hyo-Seok Kim, Joo-Yeon Kong, Jong-Hyun Kim, Seong-Chan Yeon, Il-Hwa Hong
    The Korean Journal of Parasitology.2018; 56(4): 375.     CrossRef
  • F-18-FDG PET/BT’de kolanjiosellüler kanseri taklit eden Fasciola hepatica vakası
    Hüseyin KAÇMAZ, Elif Tuğba TUNCEL, Berat EBİK, Feyzullah UÇMAK, Muhsin KAYA, Kendal YALÇIN
    Endoskopi Gastrointestinal.2018; 26(2): 69.     CrossRef
  • Unexpected hosts: imaging parasitic diseases
    Pablo Rodríguez Carnero, Paula Hernández Mateo, Susana Martín-Garre, Ángela García Pérez, Lourdes del Campo
    Insights into Imaging.2017; 8(1): 101.     CrossRef
  • Acute biliary obstruction with cholestasis caused by Fasciola hepatica in a patient travelled to Turcmenistan (a case report and literature review)
    Alexander M. Bronshteyn, N. A Malyshev, L. V Fedianina, I. V Davydova
    Epidemiology and Infectious Diseases.2016; 21(2): 92.     CrossRef
  • Monitoring of Fasciola Species Contamination in Water Dropwort by COX1 Mitochondrial and ITS-2 rDNA Sequencing Analysis
    In-Wook Choi, Hwang-Yong Kim, Juan-Hua Quan, Jae-Gee Ryu, Rubing Sun, Young-Ha Lee
    The Korean Journal of Parasitology.2015; 53(5): 641.     CrossRef
  • Endoscopic Extraction of Biliary Fascioliasis Diagnosed Using Intraductal Ultrasonography in a Patient with Acute Cholangitis
    Ji Su Ha, Hyun Jong Choi, Jong Ho Moon, Yun Nah Lee, Jae Woong Tae, Moon Han Choi, Tae Hoon Lee, Sang-Woo Cha
    Clinical Endoscopy.2015; 48(6): 579.     CrossRef
  • Prevalence of Fasciola spp. from cattle in slaughterhouse by macroscopic examination
    Bae-Keun Park, Eui-Ju Hong, Si-Yun Ryu, Bae-Dong Jung, Ji-Min Kim, Hyeon-Cheol Kim
    Korean Journal of Veterinary Service.2015; 38(4): 227.     CrossRef
  • Fasciola hepatica in Snails Collected from Water-Dropwort Fields using PCR
    Hwang-Yong Kim, In-Wook Choi, Yeon-Rok Kim, Juan-Hua Quan, Hassan Ahmed Hassan Ahmed Ismail, Guang-Ho Cha, Sung-Jong Hong, Young-Ha Lee
    The Korean Journal of Parasitology.2014; 52(6): 645.     CrossRef
  • 12,230 View
  • 143 Download
  • 19 Web of Science
  • Crossref
Four Cases of Taenia saginata Infection with an Analysis of COX1 Gene
Jaeeun Cho, Bong-Kwang Jung, Hyemi Lim, Min-Jae Kim, Thanapon Yooyen, Dongmin Lee, Keeseon S. Eom, Eun-Hee Shin, Jong-Yil Chai
Korean J Parasitol 2014;52(1):79-83.
Published online February 19, 2014
DOI: https://doi.org/10.3347/kjp.2014.52.1.79

Human taeniases had been not uncommon in the Republic of Korea (=Korea) until the 1980s. The prevalence decreased and a national survey in 2004 revealed no Taenia egg positive cases. However, a subsequent national survey in 2012 showed 0.04% (10 cases) prevalence of Taenia spp. eggs suggesting its resurgence in Korea. We recently encountered 4 cases of Taenia saginata infection who had symptoms of taeniasis that included discharge of proglottids. We obtained several proglottids from each case. Because the morphological features of T. saginata are almost indistinguishable from those of Taenia asiatica, molecular analyses using the PCR-RFLP and DNA sequencing of the cytochrome c oxidase subunit 1 (cox1) were performed to identify the species. The PCR-RFLP patterns of all of the 4 specimens were consistent with T. saginata, and the cox1 gene sequence showed 99.8-100% identity with that of T. saginata reported previously from Korea, Japan, China, and Cambodia. All of the 4 patients had the history of travel abroad but its relation with contracting taeniasis was unclear. Our findings may suggest resurgence of T. saginata infection among people in Korea.

Citations

Citations to this article as recorded by  Crossref logo
  • Molecular diagnosis of Taenia saginata from two patients in Palestine: two case reports
    Mohammad Asees, Issam Jawabreh, Omar Hamarsheh, Ziad Abdeen, Ayoub Assi, Kifaya Azmi
    Journal of Medical Case Reports.2024;[Epub]     CrossRef
  • Molecular Confirmation of Taenia solium Taeniasis in Child, Timor-Leste
    Hanna Jin, Sung-Tae Hong, Merita Antonio Armindo Monteiro, Endang da Silva, Odete da Silva Viegas, Felix dos Santos Lopes, Dong Hee Kim, Sung Hye Kim
    Emerging Infectious Diseases.2024;[Epub]     CrossRef
  • Taenia saginata Infection Misdiagnosed as Acute Cholecystitis in a Tibetan Patient, in China
    Xiu-Min Han, Xue-Yong Zhang, Ying-Na Jian, Qing-Shan Tian
    The Korean Journal of Parasitology.2021; 59(3): 311.     CrossRef
  • A co-infection case report of Taenia saginata in a patient with subclinical clonorchiasis confirmed by the combination of diagnostic tools
    Ju Hyeon Shin, Eun Jeong Won, Jee Seung Jung, Kyung-Hwa Park, Kwang Il Nam, Soo Hyun Kim, Jong Hee Shin
    BMC Infectious Diseases.2019;[Epub]     CrossRef
  • Neurocysticercosis: Clinical Characteristics and Changes from 26 Years of Experience in an University Hospital in Korea
    Hyo-Ju Son, Min Jae Kim, Kyung Hwa Jung, Sungim Choi, Jiwon Jung, Yong Pil Chong, Sung-Han Kim, Sang-Oh Lee, Sang-Ho Choi, Yang Soo Kim, Jun Hee Woo, Bong-Kwang Jung, Hyemi Song, Jong-Yil Chai
    The Korean Journal of Parasitology.2019; 57(3): 265.     CrossRef
  • Four Taeniasis saginata Cases Diagnosed at a University Hospital in Korea
    Eun Jeong Won, Ju Hyeon Shin, Yu Jeong Lee, Moon-Ju Kim, Seung Ji Kang, Sook In Jung, Soo Hyun Kim, Jong Hee Shin, Jong-Yil Chai, Sung-Shik Shin
    The Korean Journal of Parasitology.2019; 57(3): 313.     CrossRef
  • Ten Cases of Taenia saginata Infection Confirmed by Analysis of the Internal Transcribed Spacer 1 rDNA Region in the Republic of Korea
    Su-Min Song, Hae Soo Yun, Dorene VanBik, Hyun-Ha Chang, Sang-Ah Lee, Shin-Woo Kim, Namhee Ryoo, Dong Yeub Eun, Nan Young Lee, Youn-Kyoung Goo, Yeonchul Hong, Meesun Ock, Hee-Jae Cha, Dong-Il Chung
    The Korean Journal of Parasitology.2019; 57(4): 417.     CrossRef
  • Prevalence of cysticercosis in Estonian pigs and cattle
    Elisabeth Dorbek-Kolin, Tuuli Åhlberg, Lea Tummeleht, Dennis Tappe, Maria Vang Johansen, Brian Lassen
    Parasitology Research.2018; 117(2): 591.     CrossRef
  • Molecular Diagnosis of Taenia saginata Tapeworm Infection in 2 Schoolchildren, Myanmar
    Eun Jeong Won, Bong-Kwang Jung, Hyemi Song, Mi-Seon Kim, Hyun-Seung Kim, Keon Hoon Lee, Min-Jae Kim, Myung Geun Shin, Jong Hee Shin, Soon-Pal Suh, Sung-Jong Hong, Woon-Mok Sohn, Thi Thi Htoon, Htay Htay Tin, Jong-Yil Chai
    Emerging Infectious Diseases.2018; 24(6): 1156.     CrossRef
  • Genetic Characterization ofTaenia saginataCyst Isolates from Germany
    Sameh Abuseir, Sabine Schicht, Andrea Springer, Uschi Nagel-Kohl, Christina Strube
    Vector-Borne and Zoonotic Diseases.2018; 18(8): 433.     CrossRef
  • Cysticercosis/taeniasis endemicity in Southeast Asia: Current status and control measures
    Hai-Wei Wu, Akira Ito, Lin Ai, Xiao-Nong Zhou, Luz P. Acosta, Arve Lee Willingham III
    Acta Tropica.2017; 165: 121.     CrossRef
  • Molecular identification of cestodes and nematodes by cox1 gene real-time PCR and sequencing
    Rosana W.S. Poon, Emily W.T. Tam, Susanna K.P. Lau, Vincent C.C. Cheng, Kwok-Yung Yuen, Rolf K. Schuster, Patrick C.Y. Woo
    Diagnostic Microbiology and Infectious Disease.2017; 89(3): 185.     CrossRef
  • 12,036 View
  • 110 Download
  • 13 Web of Science
  • Crossref

Original Article

Diagnostic Efficacy of a Recombinant Cysteine Protease of Spirometra erinacei Larvae for Serodiagnosis of Sparganosis
S.M. Mazidur Rahman, Jae-Hwan Kim, Sung-Tae Hong, Min-Ho Choi
Korean J Parasitol 2014;52(1):41-46.
Published online February 19, 2014
DOI: https://doi.org/10.3347/kjp.2014.52.1.41

The mature domain of a cysteine protease of Spirometra erinacei plerocercoid larva (i.e., sparganum) was expressed in Escherichia coli, and its value as an antigen for the serodiagnosis of sparganosis was investigated. The recombinant protein (rSepCp-1) has the molecular weight of 23.4 kDa, and strongly reacted with the sparganum positive human or mice sera but not with negative sera by immunoblotting. ELISA with rSepCp-1 protein or sparganum crude antigen (SeC) was evaluated for the serodiagnosis of sparganosis using patient's sera. The sensitivity and specificity of ELISA using rSepCp-1 protein were 95.0% (19/20) and 99.1% (111/112), respectively. In contrast, the sensitivity and specificity of ELISA with SeC were 100% (20/20) and 96.4% (108/112), respectively. Moreover, in experimentally infected mice, the sensitivity and specificity of both ELISA assays were 100% for the detection of anti-sparganum IgG. It is suggested that the rSepCp-1 protein-based ELISA could provide a highly sensitive and specific assay for the diagnosis of sparganosis.

Citations

Citations to this article as recorded by  Crossref logo
  • Development of an immunochromatographic test for serodiagnosis of human sparganosis
    Jitaporn Harasan, Lakkhana Sadaow, Patcharaporn Boonroumkaew, Rutchanee Rodpai, Oranuch Sanpool, Hiroshi Yamasaki, Pewpan M. Intapan, Wanchai Maleewong
    Parasitology Research.2025;[Epub]     CrossRef
  • Establishment of Animal Infection Model of Spirometra Mansoni and Identification of Spirometra Mansoni by Enzyme-Linked Immunosorbent Assay
    Anqi Luo, Shuyu Chen, Mingye He, Xiaoruo Tan, Zhikang Li, Wei Liu, Yisong Liu
    Vector-Borne and Zoonotic Diseases.2024;[Epub]     CrossRef
  • Case Report: Moving Tumor-Like Foci Behind Refractory Epilepsy-Cerebral Sparganosis Successfully Treated by Surgery After Failure of Praziquantel Treatment
    Yusi Chen, Xu Chen, Huicong Kang
    Frontiers in Neurology.2022;[Epub]     CrossRef
  • Standardization of recombinant Ancylostoma caninum cysteine protease 2 (rAcCP2) based indirect ELISA for serodiagnosis of hookworm infection in dogs
    SUCHITA P UKE, RAJAT GARG, SHAFIYA IMTIAZ RAFIQI, HIRA RAM, K L KHURANA, P S BANERJEE
    The Indian Journal of Animal Sciences.2018; 88(2): 153.     CrossRef
  • Molecular Identification of Spirometra erinaceieuropaei Tapeworm in Cases of Human Sparganosis, Hong Kong
    Tommy H.C. Tang, Samson S.Y. Wong, Christopher K.C. Lai, Rosana W.S. Poon, Helen S.Y. Chan, Tak Chiu Wu, Yuk-Fai Cheung, Tak-Lap Poon, Yi-Po Tsang, Wai-Lun Tang, Alan K.L. Wu
    Emerging Infectious Diseases.2017; 23(4): 665.     CrossRef
  • Serodiagnosis of sparganosis by ELISA using recombinant cysteine protease of Spirometra erinaceieuropaei spargana
    Li Na Liu, Xi Zhang, Peng Jiang, Ruo Dan Liu, Jian Zhou, Rui Zhe He, Jing Cui, Zhong Quan Wang
    Parasitology Research.2015; 114(2): 753.     CrossRef
  • Human sparganosis, a neglected food borne zoonosis
    Quan Liu, Ming-Wei Li, Ze-Dong Wang, Guang-Hui Zhao, Xing-Quan Zhu
    The Lancet Infectious Diseases.2015; 15(10): 1226.     CrossRef
  • Clinical Features of Pulmonary Sparganosis
    Ning Li, Yi Xiang, Yun Feng, Min Li, Bei Li Gao, Qing Yun Li
    The American Journal of the Medical Sciences.2015; 350(6): 436.     CrossRef
  • Characterization of Spirometra erinaceieuropaei Plerocercoid Cysteine Protease and Potential Application for Serodiagnosis of Sparganosis
    Li Na Liu, Zhong Quan Wang, Xi Zhang, Peng Jiang, Xin Qi, Ruo Dan Liu, Zi Fang Zhang, Jing Cui, Xiao-Nong Zhou
    PLOS Neglected Tropical Diseases.2015; 9(6): e0003807.     CrossRef
  • Molecular characterization of a Spirometra mansoni antigenic polypeptide gene encoding a 28.7 kDa protein
    Jing Cui, Tong Wei, Li Na Liu, Xi Zhang, Xin Qi, Zi Fang Zhang, Zhong Quan Wang
    Parasitology Research.2014; 113(9): 3511.     CrossRef
  • Development of a Rapid Diagnostic Kit That Uses an Immunochromatographic Device To Detect Antibodies in Human Sparganosis
    Hiroshi Yamasaki, Takeshi Nakamura, Pewpan M. Intapan, Wanchai Maleewong, Yasuyuki Morishima, Hiromu Sugiyama, Hiroyuki Matsuoka, Kaoru Kobayashi, Katsuyoshi Takayama, Yukuharu Kobayashi, P. P. Wilkins
    Clinical and Vaccine Immunology.2014; 21(9): 1360.     CrossRef
  • 10,838 View
  • 70 Download
  • 12 Web of Science
  • Crossref

Brief Communications

Evaluation of IgG4 Subclass Antibody Detection by Peptide-Based ELISA for the Diagnosis of Human Paragonimiasis Heterotrema
Pewpan M. Intapan, Oranuch Sanpool, Penchom Janwan, Porntip Laummaunwai, Nimit Morakote, Yoon Kong, Wanchai Maleewong
Korean J Parasitol 2013;51(6):763-766.
Published online December 31, 2013
DOI: https://doi.org/10.3347/kjp.2013.51.6.763

A synthetic peptide was prepared based on the antigenic region of Paragonimus westermani pre-procathepsin L, and its applicability for immunodiagnosis for human paragonimiasis (due to Paragonimus heterotremus) was tested using an ELISA to detect IgG4 antibodies in the sera of patients. Sera from other helminthiases, tuberculosis, and healthy volunteers were used as the references. This peptide-based assay system gave sensitivity, specificity, accuracy, and positive and negative predictive values of 100%, 94.6%, 96.2%, 100%, and 88.9%, respectively. Cross reactivity was frequently seen against the sera of fascioliasis (75%) and hookworm infections (50%). Since differential diagnosis between paragonimiasis and fascioliasis can be easily done by clinical presentation and fascioliasis serology, this cross reaction is not a serious problem. Sera from patients with other parasitoses (0-25%) rarely responded to this synthetic antigen. This synthetic peptide antigen seems to be useful for development of a standardized diagnostic system for paragonimiasis.

Citations

Citations to this article as recorded by  Crossref logo
  • An immunochromatographic test using whole blood for rapid diagnosis of human paragonimiasis and its diagnostic usefulness
    Patcharaporn Boonroumkaew, Lakkhana Sadaow, Penchom Janwan, Rutchanee Rodpai, Oranuch Sanpool, Tongjit Thanchomnang, Hiroshi Yamasaki, Pewpan M. Intapan, Wanchai Maleewong
    Food and Waterborne Parasitology.2024; 37: e00246.     CrossRef
  • Development of point-of-care testing tool using immunochromatography for rapid diagnosis of human paragonimiasis
    Lakkhana Sadaow, Oranuch Sanpool, Hiroshi Yamasaki, Wanchai Maleewong, Pewpan M. Intapan
    Acta Tropica.2020; 203: 105325.     CrossRef
  • Paragonimus and paragonimiasis in Asia: An update
    Ayako Yoshida, Pham Ngoc Doanh, Haruhiko Maruyama
    Acta Tropica.2019; 199: 105074.     CrossRef
  • A Case of Pulmonary Paragonimiasis with Chronic Abdominal Pain and Erythematous Rash in a 6-year-old Girl
    Ju Young Kim, Min Kyu Park, Yong Ju Lee, Sun Huh, Ky Young Cho
    Pediatric Infection and Vaccine.2018; 25(1): 54.     CrossRef
  • A tool for mass-screening of paragonimiasis: an enzyme-linked immunosorbent assay with urine samples
    Xu Guang Qiu, Fukumi Nakamura-Uchiyama, Yukifumi Nawa, Makoto Itoh
    Tropical Medicine and Health.2016;[Epub]     CrossRef
  • Expression characteristics and specific antibody reactivity of diverse cathepsin F members of Paragonimus westermani
    Chun-Seob Ahn, Byoung-Kuk Na, Dong-ll Chung, Jeong-Geun Kim, Jin-Taek Kim, Yoon Kong
    Parasitology International.2015; 64(1): 37.     CrossRef
  • North American paragonimiasis: epidemiology and diagnostic strategies
    Peter U Fischer, Gary J Weil
    Expert Review of Anti-infective Therapy.2015; 13(6): 779.     CrossRef
  • 8,809 View
  • 109 Download
  • Crossref
Modified Formalin-Ether Concentration Technique for Diagnosis of Human Strongyloidiasis
Witthaya Anamnart, Pewpan M. Intapan, Wanchai Maleewong
Korean J Parasitol 2013;51(6):743-745.
Published online December 31, 2013
DOI: https://doi.org/10.3347/kjp.2013.51.6.743

We compared the efficacy and applicability of a modified formalin-ether concentration technique (M-FECT) to the conventional FECT (C-FECT) and the agar plate culture (APC) method for the detection of Strongyloides stercoralis larvae. For this purpose, we used 600 human fecal specimens collected in an endemic area of southern Thailand. In the M-FECT, we used 2 layers of wire meshes, instead of gauze, to avoid the loss by absorption/adhesion of larvae to the gauze during filtration, and we reduced the exposure time of S. stercoralis larvae in stool samples to formalin. By such simple modifications, the efficacy of M-FECT has become comparable to APC and was much better than that of C-FECT for the diagnosis of strongyloidiasis.

Citations

Citations to this article as recorded by  Crossref logo
  • Gastrointestinal Parasitic Infections in Macaca fascicularis in Northeast Thailand: A One Health Perspective on Zoonotic Risks
    Teputid Kuasit, Manachai Yingklang, Penchom Janwan, Wanchai Maleewong, Weerachai Saijuntha, Siriporn Kuanamon, Tongjit Thanchomnang
    Animals.2025; 15(14): 2112.     CrossRef
  • Strongyloidiasis
    Catherine A. Gordon, Jürg Utzinger, Stephen Muhi, Sören L. Becker, Jennifer Keiser, Virak Khieu, Darren J. Gray
    Nature Reviews Disease Primers.2024;[Epub]     CrossRef
  • Exploring the second intermediate hosts and morphology of human- and cat-specific Opisthorchis viverrini-like populations
    Vania Agustina, Prasert Saichua, Thewarach Laha, Sirikachorn Tangkawatana, Suksanti Prakobwong, Nonglak Laoprom, Wanrak Kamphasri, Chonteera Chareonchai, David Blair, Sutas Suttiprapa
    International Journal for Parasitology.2024; 54(10): 497.     CrossRef
  • Transcriptome changes of liver fluke Opisthorchis viverrini in diabetic hamsters
    Apisit Chaidee, Naruechar Charoenram, Chatchawan Sengthong, Rungtiwa Dangtakot, Porntip Pinlaor, Thatsanapong Pongking, Somchai Pinlaor
    Parasite.2024; 31: 54.     CrossRef
  • Epidemiology of Strongyloides stercoralis and Opisthorchis viverrini infections in northern and northeastern Thailand: Insights from urine-ELISA surveys
    Wansiri Wiraphongthongchai, Paiboon Sithithaworn, Kavin Thinkhamrop, Kulwadee Suwannatrai, Kulthida Y. Kopolrat, Chanika Worasith, Apiporn T. Suwannatrai
    Parasitology Research.2024;[Epub]     CrossRef
  • Intestinal helminth infections and associated risk factors among adults in the Lao People’s Democratic Republic
    Sengaloun Phonekeo, Sengchanh Kounnavong, Manithong Vonglokham, Latsamy Siengsounthone, Anousin Homsana, Sascha Gummin, Penelope Vounatsu, Prawat Nittiyanant, Suchin Worawichawong, Wichai Aekplakorn, Peter Odermatt, Somphou Sayasone
    Infectious Diseases of Poverty.2023;[Epub]     CrossRef
  • Prevalence of major nematodes and human factors that affect infection in the zebra dove in a closed cage system
    Watcharapol Suyapoh, Domechai Kaewnoi, Pornphutthachat Sota, Wichaya Thongtako, Sutas Suttiprapa
    Veterinary World.2022; : 1208.     CrossRef
  • Does Opisthorchis viverrini circulate between humans and domestic cats in an endemic area in Thailand?
    Pornphutthachat Sota, Sutas Suttiprapa, Sirikachorn Tangkawattana, Manop Sripa, David Blair, Banchob Sripa
    Parasitology.2022; 149(10): 1334.     CrossRef
  • A simple parasitological technique to increase detection of Strongyloides stercoralis in Bolivian primary health care system
    Ivana Camacho-Alvarez, Elia M. Chavez-Mamani, Goyens Philippe, Jenny M. Luizaga-López, Mary Cruz Torrico, Laurent Gétaz, Frédérique Jacobs
    BMC Primary Care.2022;[Epub]     CrossRef
  • Improved agar plate culture conditions for diagnosis of Strongyloides stercoralis
    Wannee Kaewrat, Chatchawan Sengthong, Manachai Yingklang, Kitti Intuyod, Ornuma Haonon, Sudarat Onsurathum, Rungtiwa Dangtakot, Phitsamai Saisud, Arunnee Sangka, Sirirat Anutrakulchai, Somchai Pinlaor, Ubon Cha'on, Porntip Pinlaor
    Acta Tropica.2020; 203: 105291.     CrossRef
  • Comparative study of two commercial tests for Strongyloides stercoralis serologic diagnosis
    Isabel Fradejas, J M Herrero-Martínez, Manuel Lizasoaín, Esperanza Rodríguez de las Parras, Ana Pérez-Ayala
    Transactions of The Royal Society of Tropical Medicine and Hygiene.2018;[Epub]     CrossRef
  • Strongyloides stercoralis larvae found for the first time in tap water using a novel culture method
    Ayman A. El-Badry, Doaa A. Hamdy, Wegdan M. Abd El Wahab
    Parasitology Research.2018; 117(12): 3775.     CrossRef
  • Risk factors for Opisthorchis viverrini infection in Nakhon Phanom, Thailand, where the infection is highly endemic
    Songkran Nakbun, Pramote Thongkrajai, Choosak Nithikathkul
    Asian Biomedicine.2018; 12(1): 45.     CrossRef
  • Limitations to the adoption of a standardized Strongyloides stercoralis diagnostic method: Case study in the Caribbean
    Jennifer K. Ketzis
    Acta Tropica.2017; 170: 178.     CrossRef
  • Prevalence of gastrointestinal helminth parasites of zoonotic significance in dogs and cats in lower Northern Thailand
    Wilawan PUMIDONMING, Doaa SALMAN, Dulyatad GRONSANG, Abdelbaset E. ABDELBASET, Khamphon SANGKAEO, Shin-ichiro KAWAZU, Makoto IGARASHI
    Journal of Veterinary Medical Science.2016; 78(12): 1779.     CrossRef
  • Novel approaches to the diagnosis of Strongyloides stercoralis infection
    D. Buonfrate, F. Formenti, F. Perandin, Z. Bisoffi
    Clinical Microbiology and Infection.2015; 21(6): 543.     CrossRef
  • 10,142 View
  • 122 Download
  • Crossref
Serological and Molecular Characteristics of the First Korean Case of Echinococcus multilocularis
Jin-Sook Jeong, Sang-Young Han, Young-Hoon Kim, Yasuhito Sako, Tetsuya Yanagida, Akira Ito, Jong-Yil Chai
Korean J Parasitol 2013;51(5):595-597.
Published online October 31, 2013
DOI: https://doi.org/10.3347/kjp.2013.51.5.595

In December 2011, we reported an autochthonous case of Echinococcus multilocularis infection in a 42-year-old woman in Korea. The diagnosis was based on histopathological findings of the surgically resected liver cyst. In the present study, we evaluated the serological and molecular characteristics of this Korean E. multilocularis case. The patient's serum strongly reacted with affinity-purified native Em18 and recombinant Em18 antigens (specific for E. multilocularis) but negative for recombinant antigen B8/1 (reactive for Echinococcus granulosus). In immunoaffinity chromatography, the serum also strongly reacted with E. multilocularis and only weakly positive for E. granulosus. We determined the whole nucleotide sequence of cox1 (1,608 bp) using the paraffin-embedded cystic tissue which was compared with E. multilocularis isolates from China, Japan, Kazakhstan, Austria, France, and Slovakia. The Korean case showed 99.8-99.9% similarity with isolates from Asia (the highest similarity with an isolate from Sichuan, China), whereas the similarity with European isolates ranged from 99.5 to 99.6%.

Citations

Citations to this article as recorded by  Crossref logo
  • Worldwide literature on epidemiology of human alveolar echinococcosis: a systematic review of research published in the twenty-first century
    Sven Baumann, Rong Shi, Wenya Liu, Haihua Bao, Julian Schmidberger, Wolfgang Kratzer, Weixia Li, Thomas F. E. Barth, Sven Baumann, Johannes Bloehdorn, Iris Fischer, Tilmann Graeter, Natalja Graf, Beate Gruener, Doris Henne-Bruns, Andreas Hillenbrand, Tanj
    Infection.2019; 47(5): 703.     CrossRef
  • Lasiopodomys fuscus as an important intermediate host for Echinococcus multilocularis: isolation and phylogenetic identification of the parasite
    Qi-Gang Cai, Xiu-Min Han, Yong-Hai Yang, Xue-Yong Zhang, Li-Qing Ma, Panagiotis Karanis, Yong-Hao Hu
    Infectious Diseases of Poverty.2018;[Epub]     CrossRef
  • Assessment of the global pattern of genetic diversity in Echinococcus multilocularis inferred by mitochondrial DNA sequences
    Adel Spotin, Belgees Boufana, Ehsan Ahmadpour, Adriano Casulli, Mahmoud Mahami-Oskouei, Soheila Rouhani, Amirreza Javadi-Mamaghani, Firooz Shahrivar, Paria Khoshakhlagh
    Veterinary Parasitology.2018; 262: 30.     CrossRef
  • The echinococcoses in Asia: The present situation
    Akira Ito, Christine M. Budke
    Acta Tropica.2017; 176: 11.     CrossRef
  • 8,866 View
  • 98 Download
  • Crossref

Case Report

Molecular Diagnosis of an Ocular Toxocariasis Patient in Vietnam
Nguyen Van De, Nguyen Vu Trung, Le Van Duyet, Jong-Yil Chai
Korean J Parasitol 2013;51(5):563-567.
Published online October 31, 2013
DOI: https://doi.org/10.3347/kjp.2013.51.5.563

An ocular Toxocara canis infection is reported for the first time in Vietnam. A 34-year-old man residing in a village of Son La Province, North Vietnam, visited the National Eye Hospital (NEH) in August 2011. He felt a bulge-sticking pain in his left eye and loss of vision occurred over 3 months before visiting the hospital. The eye examination in the hospital showed damage of the left eye, red eye, retinal fibrosis, retinal detachment, inflammation of the eye tissues, retinal granulomas, and a parasitic cyst inside. A larva of Toxocara was collected with the cyst by a medical doctor by surgery. Comparison of 264 nucleotides of internal transcribed spacer 2 (ITS2) of ribosomal DNA was done between our Vietnamese Toxocara canis and other Toxocara geographical isolates, including Chinese T. canis, Japanese T. canis, Sri Lankan T. canis, and Iranian T. canis. The nucleotide homology was 97-99%, when our T. canis was compared with geographical isolates. Identification of a T. canis infection in the eye by a molecular method was performed for the first time in Vietnam.

Citations

Citations to this article as recorded by  Crossref logo
  • Toxocara cati Infection in Cats (Felis catus): A Systematic Review and Meta-Analysis
    Jorge Luis Bonilla-Aldana, Alba Cristina Espinosa-Nuñez, D. Katterine Bonilla-Aldana, Alfonso J. Rodriguez-Morales
    Animals.2024; 14(7): 1022.     CrossRef
  • An Integrated Coproscopic and Molecular Method Provides Insights into the Epidemiology of Zoonotic Intestinal Helminths of Dogs across Cambodia
    Patsy A. Zendejas-Heredia, Vito Colella, Lucas G. Huggins, Roland Schaper, Bettina Schunack, Rebecca J. Traub, Long-Xian Zhang
    Transboundary and Emerging Diseases.2023; 2023: 1.     CrossRef
  • An overview of human helminthioses in Vietnam: Their prevention, control and lessons learnt
    Hung Manh Nguyen, Dung Trung Do, Stephen E. Greiman, Ha Van Nguyen, Hien Van Hoang, Toan Quoc Phan, Phuc Pham-Duc, Henry Madsen
    Acta Tropica.2023; 238: 106753.     CrossRef
  • A delayed diagnosis of ocular toxocariasis presenting as total monocular retinal detachment in an immunocompetent 57-year-old male
    George W. Jowsey, Gavin X. McLeod
    IDCases.2023; 32: e01764.     CrossRef
  • Molecular and microscopic detection of natural and experimental infections of Toxocara vitulorum in bovine milk
    Amira Dewair, Mohamed Bessat, Jacopo Guccione
    PLOS ONE.2020; 15(5): e0233453.     CrossRef
  • Toxocariasis: a silent threat with a progressive public health impact
    Jia Chen, Quan Liu, Guo-Hua Liu, Wen-Bin Zheng, Sung-Jong Hong, Hiromu Sugiyama, Xing-Quan Zhu, Hany M. Elsheikha
    Infectious Diseases of Poverty.2018;[Epub]     CrossRef
  • Detection of Toxocara canis DNA in tissues of experimentally infected mice
    Micaele Quintana de Moura, Marcia Raquel Pegoraro de Macedo, Wesley Douglas da Silva Terto, Luciana Farias da Costa Avila, Fabio Pereira Leivas Leite, Carlos James Scaini, Natália Berne Pinto, Gabriela de Almeida Capella, Adriane Leites Strothmann, Marcos
    Acta Tropica.2018; 187: 51.     CrossRef
  • Dot enzyme-linked immunosorbent assay (ELISA) for the detection of Toxocara infection using a rat model
    Vachel Gay V. Paller, Cyrelle M. Besana, Isabel Kristine M. Valdez
    Journal of Parasitic Diseases.2017; 41(4): 933.     CrossRef
  • Levels of Toxocara infections in dogs and cats from urban Vietnam together with associated risk factors for transmission
    N. Thi Lan Anh, D. Thi Thu Thuy, D. Huu Hoan, N. Thi Hop, D. Trung Dung
    Journal of Helminthology.2016; 90(4): 508.     CrossRef
  • Seroprevalence of fascioliasis, toxocariasis, strongyloidiasis and cysticercosis in blood samples diagnosed in Medic Medical Center Laboratory, Ho Chi Minh City, Vietnam in 2012
    Toan Nguyen, Fei Wen Cheong, Jonathan Wee Kent Liew, Yee Ling Lau
    Parasites & Vectors.2016;[Epub]     CrossRef
  • Field evaluation of a rapid diagnostic test to detect antibodies in human toxocariasis
    P.K.C. Lim, H. Yamasaki, J.W. Mak, S.F. Wong, C.W. Chong, I.K.S. Yap, S. Ambu, V. Kumarasamy
    Acta Tropica.2015; 148: 32.     CrossRef
  • 9,353 View
  • 94 Download
  • Crossref

Original Article

A Rapid Diagnostic Test for Toxoplasmosis using Recombinant Antigenic N-terminal Half of SAG1 Linked with Intrinsically Unstructured Domain of GRA2 Protein
Kyoung Ju Song, Zhaoshou Yang, Chom-Kyu Chong, Jin-Soo Kim, Kyung Chan Lee, Tong-Soo Kim, Ho-Woo Nam
Korean J Parasitol 2013;51(5):503-510.
Published online October 31, 2013
DOI: https://doi.org/10.3347/kjp.2013.51.5.503

Toxoplasma gondii is an apicomplexan parasite with a broad host range of most warm-blooded mammals including humans, of which one-thirds of the human population has been infected worldwide which can cause congenital defects, abortion, and neonatal complications. Here, we developed a rapid diagnostic test (RDT) for T. gondii infection. Antigenic N-terminal half of the major surface antigen (SAG1) was linked with intrinsically unstructured domain (IUD) of dense granule protein 2 (GRA2). The recombinant GST-GRA2-SAG1A protein was successfully expressed and purified as 51 kDa of molecular weight. Furthermore, antigenicity and solubility of the rGST-GRA2-SAG1A protein were significantly increased. The overall specificity and sensitivity of GST-GRA2-SAG1A loaded RDT (TgRDT) were estimated as 100% and 97.1% by comparing with ELISA result which uses T. gondii whole cell lysates as the antigen. The TgRDT tested with Uganda people sera for field trial and showed 31.9% of seroprevalence against T. gondii antibody. The TgRDT is proved to be a kit for rapid and easy to use with high accuracy, which would be a suitable serodiagnostic tool for toxoplasmosis.

Citations

Citations to this article as recorded by  Crossref logo
  • Development of an Immunochromatographic Test with Recombinant MIC2-MIC3 Fusion Protein for Serological Detection of Toxoplasma gondii
    Jianzhong Wang, Yi Zhao, Jicheng Qiu, Jing Liu, Rui Zhou, Xialin Ma, Xiaojie Wu, Xiaoguang Li, Wei Mao, Yiduo Liu, Heng Zhang
    Veterinary Sciences.2025; 12(6): 509.     CrossRef
  • Application of gold immunochromatographic assay strip combined with digital evaluation for early detection of Toxoplasma gondii infection in multiple species
    Jiyuan Fan, Hao Sun, Jiawen Fang, Yafan Gao, Haojie Ding, Bin Zheng, Qingming Kong, Xunhui Zhuo, Shaohong Lu
    Parasites & Vectors.2024;[Epub]     CrossRef
  • Single Cell Expression Systems for the Production of Recombinant Proteins for Immunodiagnosis and Immunoprophylaxis of Toxoplasmosis
    Karolina Sołowińska, Lucyna Holec-Gąsior
    Microorganisms.2024; 12(8): 1731.     CrossRef
  • Seroprevalence of Toxoplasma gondii infection among patients of a tertiary hospital in Guangzhou, Guangdong province, PR China
    Yu-bin Guan, Xiao-xiao Sun, Shao-lian Chen, Xiao-ting Zhu, Zhi-hua Zeng, Han-wei Lu, Hong-mei Feng, Yu Guo, Wen-gong Jiang, Kui Xiong, Xiao-rong Yang, Ho-Woo Nam, Zhao-shou Yang, Pan Li
    PLOS ONE.2023; 18(7): e0286430.     CrossRef
  • Past and present seroprevalence and disease burden estimates of Toxoplasma gondii infections in Germany: An appreciation of the role of serodiagnostics
    Frank Seeber
    International Journal of Medical Microbiology.2023; 313(6): 151592.     CrossRef
  • Seroprevalence of Toxoplasma gondii assayed using Rapid Diagnostic Tests among Residents in Three Counties Adjacent to The Demilitarized Zone, Korea
    Jeehi Jung, Jinyoung Lee, Yoon Kyung Chang, Seong Kyu Ahn, Seo Hye Park, Sung-Jong Hong, Jihoo Lee, Chom-Kyu Chong, Hye-Jin Ahn, Ho-Woo Nam, Tong-Soo Kim, Dongjae Kim
    The Korean Journal of Parasitology.2021; 59(1): 9.     CrossRef
  • Clusters of Toxoplasmosis in Ganghwa-gun, Cheorwon-gun, and Goseong-gun, Korea
    Jihye Yu, Woojin Kim, Yoon Kyung Chang, Tong-Soo Kim, Sung-Jong Hong, Hye-Jin Ahn, Ho-Woo Nam, Dongjae Kim
    The Korean Journal of Parasitology.2021; 59(3): 251.     CrossRef
  • Serological and molecular rapid diagnostic tests for Toxoplasma infection in humans and animals
    Amjad Hayat Khan, Rahmah Noordin
    European Journal of Clinical Microbiology & Infectious Diseases.2020; 39(1): 19.     CrossRef
  • Clusters of Toxoplasmosis in Gyodong-Myeon and Samsan-Myeon, Ganghwa-Gun, Korea
    Woojin Kim, Yoon Kyung Chang, Tong-Soo Kim, Sung-Jong Hong, Hye-Jin Ahn, Ho-Woo Nam, Dongjae Kim
    The Korean Journal of Parasitology.2020; 58(5): 493.     CrossRef
  • Identification of novel antigens for serum IgG diagnosis of human toxoplasmosis
    Juntao Luo, Jingyi Wan, Ziru Tang, Shuang Shen
    Experimental Parasitology.2019; 204: 107722.     CrossRef
  • Seroprevalence of Toxoplasmosis with ELISA and Rapid Diagnostic Test among Residents in Gyodong-do, Inchon city, Korea: A Four-Year Follow-up
    Yeong Hoon Kim, Ji hoo Lee, Seong kyu Ahn, Tong-Soo Kim, Sung-Jong Hong, Chom-Kyu Chong, Hye-Jin Ahn, Ho-Woo Nam
    The Korean Journal of Parasitology.2017; 55(3): 247.     CrossRef
  • Development of direct assays for Toxoplasma gondii and its use in genomic DNA sample
    Lívia M. Alves, Vinícius R. Rodovalho, Ana C.H. Castro, Márcia A.R. Freitas, Caroline M. Mota, Tiago W.P. Mineo, José R. Mineo, João M. Madurro, Ana G. Brito-Madurro
    Journal of Pharmaceutical and Biomedical Analysis.2017; 145: 838.     CrossRef
  • Seroprevalence of Toxoplasmosis Detected by RDT in Residents near the DMZ (demilitarized zone) of Cheorwon-gun, Gangwon-do, Korea
    Yeong Hoon Kim, Jihoo Lee, Young-Eun Kim, Seongkyu Ahn, Tong-Soo Kim, Sung-Jong Hong, Chom-Kyu Chong, Hye-Jin Ahn, Ho-Woo Nam
    The Korean Journal of Parasitology.2017; 55(4): 385.     CrossRef
  • Western Blot Detection of Human Anti-Chikungunya Virus Antibody with Recombinant Envelope 2 Protein
    Zhaoshou Yang, Jihoo Lee, Hye-Jin Ahn, Chom-Kyu Chong, Ronaldo F. Dias, Ho-Woo Nam
    The Korean Journal of Parasitology.2016; 54(2): 239.     CrossRef
  • Digested disorder, Quarterly intrinsic disorder digest (October-November-December, 2013)
    Shelly DeForte, Krishna D Reddy, Vladimir N Uversky
    Intrinsically Disordered Proteins.2015; 3(1): e984569.     CrossRef
  • Probability of Antibody Formation against Circumsporozoite Protein of Plasmodium vivax among Korean Malaria Patients
    Ho-Woo Nam, Kyoung Ju Song, Hye Jin Ahn, Zhaoshou Yang, Chom-Kyu Chong, Pyo Yun Cho, Seong Kyu Ahn, Tong-Soo Kim
    The Korean Journal of Parasitology.2014; 52(2): 143.     CrossRef
  • High Expression of Water-Soluble Recombinant Antigenic Domains ofToxoplasma gondii Secretory Organelles
    Zhaoshou Yang, Hye-Jin Ahn, Ho-Woo Nam
    The Korean Journal of Parasitology.2014; 52(4): 367.     CrossRef
  • 9,683 View
  • 106 Download
  • Crossref

Brief Communication

IgG Western Blot for Confirmatory Diagnosis of Equivocal Cases of Toxoplasmosis by EIA-IgG and Fluorescent Antibody Test
Imen Khammari, Fatma Saghrouni, Alia Yaacoub, Sondoss Gaied Meksi, Hinda Ach, Lamia Garma, Akila Fathallah, Moncef Ben Sa?d
Korean J Parasitol 2013;51(4):485-488.
Published online August 30, 2013
DOI: https://doi.org/10.3347/kjp.2013.51.4.485

The performance values of available techniques used in serodiagnosis of toxoplasmosis are satisfactory but they raise problems of equivocal and discordant results for very low IgG titers. Recently marketed, LDBio-Toxo II IgG Western blot (IB) showed an excellent correlation with the dye test. We estimated the proportion of equivocal and discordant results between the enzyme immunoassay Platelia Toxo IgG (EIA-IgG) and fluorescent antibody test (FAT) and assessed the usefulness of the IB as a confirmatory test. Out of 2,136 sera collected from pregnant women, 1,644 (77.0%) tested unequivocally positive and 407 (19.0%) were negative in both EIA-IgG and FAT. The remaining 85 (4%) sera showed equivocal or discordant results. Among them, 73 (85.9%) were positive and 12 (14.1%) were negative in IB. Forty-one (89.1%) equivocal sera in EIA-IgG and 46 (86.8%) equivocal sera in FAT were positive in IB. Reducing the cut-off values of both screening techniques improved significantly their sensitivity in detecting very low IgG titers at the expense of their specificity. In conclusion, equivocal results in routine-used techniques and their discordance in determination of the immune status in pregnancy women were not uncommon. IB test appeard to be highly useful in these situations as a confirmatory technique.

Citations

Citations to this article as recorded by  Crossref logo
  • Systematic Review and Meta-Analysis of Congenital Toxoplasmosis Diagnosis: Advances and Challenges
    Priscila Silva Franco, Ana Carolina Morais Oliveira Scussel, Rafaela José Silva, Thadia Evelyn Araújo, Henrique Tomaz Gonzaga, Camila Ferreira Marcon, Joaquim Pedro Brito-de-Sousa, Angélica Lemos Debs Diniz, Marina Carvalho Paschoini, Bellisa Freitas Barb
    Journal of Tropical Medicine.2024; 2024: 1.     CrossRef
  • Congenital Toxoplasmosis Diagnosis: Current Approaches and New Insights
    Alfredo Márquez-Mauricio, Heriberto Caballero-Ortega, Fernando Gómez-Chávez
    Acta Parasitologica.2023; 68(3): 473.     CrossRef
  • Performances of ICT Toxoplasma IgG-IgM test in comparison with Vidas® toxo competition to determine the immune status against Toxoplasma gondii
    Sylvie Abraham, Raphael Piarroux, Ying Zhou, Vera Tesic, Ana Abeleda, Nadhira Houhou-Fidouh, Pascale Nicaise-Rolland, Luce Landraud, Rima McLeod, Sandrine Houzé
    European Journal of Clinical Microbiology & Infectious Diseases.2023; 42(11): 1327.     CrossRef
  • Determination of an optimal ELISA cut-off for the diagnosis of Toxoplasma gondii infection in pigs using Bayesian latent class modelling of data from multiple diagnostic tests
    Abbey Olsen, Henrik Vedel Nielsen, Lis Alban, Hans Houe, Tina Birk Jensen, Matthew Denwood
    Preventive Veterinary Medicine.2022; 201: 105606.     CrossRef
  • Diagnostic Accuracy of LDBIO-Toxo II IgG and IgM Western Blot in Suspected Seroconversion in Pregnancy: A Multicentre Study
    Valeria Meroni, Francesca Genco, Luigia Scudeller, Marie-Pierre Brenier-Pinchart, Hélène Fricker-Hidalgo, Coralie L’Ollivier, Luc Paris, Hervé Pelloux
    Pathogens.2022; 11(6): 665.     CrossRef
  • Difficultés d’interprétation de la sérologie toxoplasmose
    Luc Paris, Sandrine Houzé
    Revue Francophone des Laboratoires.2022; 2022(545): 33.     CrossRef
  • Serological diagnosis of toxoplasmosis: evaluation of the commercial test recomLine Toxoplasma IgG immunoblot (Mikrogen) based on recombinant antigens
    Vincent Jean-Pierre, Julien Miozzo, Hélène Fricker-Hidalgo, Cécile Garnaud, Marie Gladys Robert, Hervé Pelloux, Marie-Pierre Brenier-Pinchart
    Parasite.2022; 29: 52.     CrossRef
  • Contribution of the Toxoplasma ICT IgG IgM® test in determining the immune status of pregnant women against toxoplasmosis
    Ben‐Abdallah Rym, Kalboussi Yasmine, Bellali Hedia, Issaoui Nesrine, Souissi Olfa, Maatoug Rania, Aoun Karim, Bouratbine Aïda
    Journal of Clinical Laboratory Analysis.2021;[Epub]     CrossRef
  • A longitudinal study of Toxoplasma gondii seroconversion on four large Danish sow farms
    Abbey Olsen, Lis Alban, Matthew Denwood, Hans Houe, Tina Birk Jensen, Henrik Vedel Nielsen
    Veterinary Parasitology.2021; 295: 109460.     CrossRef
  • Contribution of the "Recomline Toxoplasma IgM" Kit in the Distinction between Toxoplasmic IgM and Natural IgM
    Khammari Imen, Ben Halima Nada, Ismaïl Samar, Chouaieb Hamed, Fathallah Akila
    International Journal Of Pharmaceutical And Phytopharmacological Research.2021; 11(6): 15.     CrossRef
  • Evaluating the “Recomline Toxoplasma IgM” Kit for Differentiating Toxoplasmic and Natural IgM
    Imen Khammari, Nada Ben Halima, Samar Ismaïl, Hamed Chouaieb, Akila Fathallah
    Interdisciplinary Research in Medical Sciences Specialty.2021; 1(2): 1.     CrossRef
  • Performance of a Toxo IgM prototype assay for the diagnosis of maternal and congenital Toxoplasma infections
    Martine Wallon, Hélène Fricker-Hidalgo, Emmanuelle Chapey, Claire Bailet, Céline Dard, Marie-Pierre Brenier-Pinchart, Hervé Pelloux
    Clinical Chemistry and Laboratory Medicine (CCLM).2020; 58(11): 1959.     CrossRef
  • Performance of Zika Assays in the Context of Toxoplasma gondii, Parvovirus B19, Rubella Virus, and Cytomegalovirus (TORCH) Diagnostic Assays
    Bettie Voordouw, Barry Rockx, Thomas Jaenisch, Pieter Fraaij, Philippe Mayaud, Ann Vossen, Marion Koopmans
    Clinical Microbiology Reviews.2019;[Epub]     CrossRef
  • Establishing tools for early diagnosis of congenital toxoplasmosis: Flow cytometric IgG avidity assay as a confirmatory test for neonatal screening
    Aline de Castro Zacche-Tonini, Giuliana Schmidt França Fonseca, Laura Néspoli Nassar Pansini de Jesus, Geisa Baptista Barros, Jordana Grazziela Alves Coelho-dos-Reis, Samantha Ribeiro Béla, Anderson Silva Machado, Ana Carolina Aguiar Vasconcelos Carneiro,
    Journal of Immunological Methods.2017; 451: 37.     CrossRef
  • A New IgG Immunoblot Kit for Diagnosis of Toxoplasmosis in Pregnant Women
    Imen Khammari, Fatma Saghrouni, Sami Lakhal, Aida Bouratbine, Moncef Ben Said, Jalel Boukadida
    The Korean Journal of Parasitology.2014; 52(5): 493.     CrossRef
  • Identification of soluble and membrane antigenic markers of acquired toxoplasmosis by immunoblot
    I. Khammari, F. Saghrouni, S. Lakhal, I. Bougmiza, A. Bouratbine, M. Ben Said, J. Boukadida
    Parasite Immunology.2014; 36(12): 684.     CrossRef
  • 8,763 View
  • 98 Download
  • Crossref

Case Reports

A Case of Diphyllobothrium nihonkaiense Infection as Confirmed by Mitochondrial COX1 Gene Sequence Analysis
Sang Hyun Park, Keeseon S. Eom, Min Sun Park, Oh Kyoung Kwon, Hyo Sun Kim, Jai Hoon Yoon
Korean J Parasitol 2013;51(4):471-473.
Published online August 30, 2013
DOI: https://doi.org/10.3347/kjp.2013.51.4.471

Diphyllobothrium nihonkaiense has been reported in Korea as Diphyllobothrium latum because of their close morphologic resemblance. We have identified a human case of D. nihonkaiense infection using the mitochondrial cytochrome c oxidase subunit I (cox1) gene sequence analysis. On 18 February 2012, a patient who had consumed raw fish a month earlier visited our outpatient clinic with a long tapeworm parasite excreted in the feces. The body of the segmented worm was 2 m long and divided into the scolex (head) and proglottids. It was morphologically close to D. nihonkaiense and D. latum. The cox1 gene analysis showed 99.4% (340/342 bp) homology with D. nihonkaiense but only 91.8% (314/342 bp) homology with D. latum. The present study suggested that the Diphyllobothrium spp. infection in Korea should be analyzed with specific DNA sequence for an accurate species identification.

Citations

Citations to this article as recorded by  Crossref logo
  • Dietary footprints of a global parasite: diagnosing Dibothriocephalus nihonkaiensis in non-endemic regions
    Wilson G.W. Goh, Jean-Marc Chavatte, Gabriel Z.R. Yan, Yuan Yi Constance Chen, Mark Dhinesh Muthiah, Lionel H.W. Lum
    Gut Pathogens.2025;[Epub]     CrossRef
  • Repertory of eukaryotes (eukaryome) in the human gastrointestinal tract: taxonomy and detection methods
    I. Hamad, D. Raoult, F. Bittar
    Parasite Immunology.2016; 38(1): 12.     CrossRef
  • Diphyllobothrium nihonkaiense: wide egg size variation in 32 molecularly confirmed adult specimens from Korea
    Seoyun Choi, Jaeeun Cho, Bong-Kwang Jung, Deok-Gyu Kim, Sarah Jiyoun Jeon, Hyeong-Kyu Jeon, Keeseon S. Eom, Jong-Yil Chai
    Parasitology Research.2015; 114(6): 2129.     CrossRef
  • Three Cases of Diphyllobothrium nihonkaiense Infection in Korea
    Hong-Ja Kim, Keeseon S. Eom, Min Seo
    The Korean Journal of Parasitology.2014; 52(6): 673.     CrossRef
  • Extracorporeal Worm Extraction of Diphyllobothrium nihonkaiense with Amidotrizoic Acid in a Child
    Hye Kyung Shin, Joo-Hyung Roh, Jae-Won Oh, Jae-Sook Ryu, Youn-Kyoung Goo, Dong-Il Chung, Yong Joo Kim
    The Korean Journal of Parasitology.2014; 52(6): 677.     CrossRef
  • Two Human Cases of Diphyllobothrium nihonkaiense Infection in Korea
    Su-Min Song, Hye-Won Yang, Min Kyu Jung, Jun Heo, Chang Min Cho, Youn-Kyoung Goo, Yeonchul Hong, Dong-Il Chung
    The Korean Journal of Parasitology.2014; 52(2): 197.     CrossRef
  • Parasitic Infections Based on 320 Clinical Samples Submitted to Hanyang University, Korea (2004-2011)
    Sung-Chul Choi, Soo-Young Lee, Hyun-Ouk Song, Jae-Sook Ryu, Myoung-Hee Ahn
    The Korean Journal of Parasitology.2014; 52(2): 215.     CrossRef
  • 8,812 View
  • 82 Download
  • Crossref
Cutaneous Gnathostomiasis with Recurrent Migratory Nodule and Persistent Eosinophilia: a Case Report from China
Jing Cui, Ye Wang, Zhong Quan Wang
Korean J Parasitol 2013;51(4):467-470.
Published online August 30, 2013
DOI: https://doi.org/10.3347/kjp.2013.51.4.467

The present study reports a human case of cutaneous gnathostomiasis with recurrent migratory nodule and persistent eosinophilia in China. A 52-year-old woman from Henan Province, central China, presented with recurrent migratory reddish swelling and subcutaneous nodule in the left upper arm and on the back for 3 months. Blood examination showed eosinophila (21.2%), and anti-sparganum antibodies were positive. Skin biopsy of the lesion and histopathological examinations revealed dermal infiltrates of eosinophils but did not show any parasites. Thus, the patient was first diagnosed as sparganosis; however, new migratory swellings occurred after treatment with praziquantel for 3 days. On further inquiring, she recalled having eaten undercooked eels and specific antibodies to the larvae of Gnathostoma spinigerum were detected. The patient was definitely diagnosed as cutaneous gnathostomiasis caused by Gnathostoma sp. and treated with albendazole (1,000 mg/day) for 15 days, and the subsequent papule and blister developed after the treatment. After 1 month, laboratory findings indicated a reduced eosinophil count (3.3%). At her final follow-up 18 months later, the patient had no further symptoms and anti-Gnathostoma antibodies became negative. Conclusively, the present study is the first report on a human case of cutaneous gnathostomiasis in Henan Province, China, based on the past history (eating undercooked eels), clinical manifestations (migratory subcutaneous nodule and persistent eosinophilia), and a serological finding (positive for specific anti-Gnathostoma antibodies).

Citations

Citations to this article as recorded by  Crossref logo
  • First reported case of intraocular gnathostomiasis in China
    Shuang Wang, Ling Zhang, Feng Miao, Jun Huang, Juan Guo
    Journal of Travel Medicine.2022;[Epub]     CrossRef
  • Current and future strategies against cutaneous parasites
    Ernest Man, Helen P. Price, Clare Hoskins
    Pharmaceutical Research.2022; 39(4): 631.     CrossRef
  • Eosinophilic Meningitis (Angiostrongylus spp. and Gnathostoma spp.)
    Nelson Iván Agudelo Higuita, Jackrapong Bruminhent
    Current Tropical Medicine Reports.2022; 9(1): 40.     CrossRef
  • Morphological and Phylogenetic Analysis of Eustrongylides sp. and Gnathostoma spinigerum Parasitizing the Asian Swamp Eel Monopterusalbus in China
    Sixin Zhang, Guangping Huang, Liang Li, Xianyong Liu, Xiaoli Tang, Xun Suo
    Pathogens.2021; 10(6): 711.     CrossRef
  • Human gnathostomiasis: a neglected food-borne zoonosis
    Guo-Hua Liu, Miao-Miao Sun, Hany M. Elsheikha, Yi-Tian Fu, Hiromu Sugiyama, Katsuhiko Ando, Woon-Mok Sohn, Xing-Quan Zhu, Chaoqun Yao
    Parasites & Vectors.2020;[Epub]     CrossRef
  • Imported gnathostomiasis manifesting as cutaneous larva migrans and Löffler’s syndrome
    William L. Hamilton, Daniel Agranoff
    BMJ Case Reports.2018; 2018: bcr-2017-223132.     CrossRef
  • 12,906 View
  • 175 Download
  • Crossref

Original Article

Serodiagnosis of Toxocariasis by ELISA Using Crude Antigen of Toxocara canis Larvae
Yan Jin, Chenghua Shen, Sun Huh, Woon-Mok Sohn, Min-Ho Choi, Sung-Tae Hong
Korean J Parasitol 2013;51(4):433-439.
Published online August 30, 2013
DOI: https://doi.org/10.3347/kjp.2013.51.4.433

Toxocariasis is a worldwide zoonosis caused by larvae of ascarid nematodes of dogs or cats, Toxocara canis or T. cati. Diagnosis of human toxocariasis currently relies on serology that uses T. canis excretory-secretory antigen to detect specific IgG antibodies by ELISA. We investigated the serodiagnostic efficacy of ELISA using crude antigen of T. canis larvae (TCLA). Serum specimens of 64 clinically confirmed toxocariasis, 115 healthy controls, and 119 other tissue-invading helminthiases were screened by ELISA using TCLA. The ELISA using TCLA showed 92.2% (59/64 patient samples) sensitivity and 86.6% (103/119) specificity. Its positive diagnostic predictivity was 78.7% and negative predictivity was 97.8%. No serum of healthy controls reacted but that of anisakiasis (45.5%), gnathostomiasis (19.2%), clonorchiasis (15.8%), sparganosis (11.1%), and cysticercosis (6.3%) cross-reacted. Immunoblot analysis on TCLA recognized antigenic proteins of 28- and 30-kDa bands in their dominant protein quantity and strong blotting reactivity. The present results indicate that the ELISA using our TCLA antigen is acceptable by the sensitivity and specificity for serodiagnosis of human toxocariasis. ELISA with TCLA is recommended to make differential diagnosis for patients with any sign of organ infiltration and eosinophilia.

Citations

Citations to this article as recorded by  Crossref logo
  • Intermediate Uveitis: An Updated Review of the Differential Diagnosis and Relevant Special Investigations
    Jacob Biju Mark, Derrick P. Smit, Rajashree E, Rathinam SR
    Ocular Immunology and Inflammation.2025; 33(4): 522.     CrossRef
  • Análisis serológico de Toxocara canis y Toxocara cati por ELISA en niños de una escuela de educación básica de la provincia de Chimborazo
    Laura Katheryne Hernández León, Sandra Noemí Escobar Arrieta, Verónica Mercedes Cando Brito
    Anatomía Digital.2025; 8(2.2): 93.     CrossRef
  • Epidemiological profile of human toxocariasis in patients examined at Evandro Chagas Institute (IEC/SVSA/MS) between 2014 and 2019
    Lucas Solano Araújo da Silva, Isabelle Helena Lima Dias, Álvaro Luan Santana Fonseca, Martin Johannes Enk, Joyce Favacho Cardoso Nogueira, Ricardo José de Paula Souza e Guimarães, Christiane de Oliveira Goveia
    Comparative Immunology, Microbiology and Infectious Diseases.2024; 105: 102112.     CrossRef
  • Evaluation of Somatic Antigens of Adult Toxocara helminthes for Detection of Human Toxocariasis
    Zahra Navi, Reza Falak, Mehdi Mohebali, Mohammad Bagher Molairad, Zabihollah Zarei, Mojgan Aryaeipour, Abbas Rahimi Foroushani, Mohammad Zibaei, Mohammad Bagher Rokni
    Parasite Immunology.2024;[Epub]     CrossRef
  • Toxocara canis and Fasciola hepatica Co-Infection Leading to Hepatic Abscess: A Case Report
    Seung Wan Kim, Byoung Kuk Jang
    Journal of Korean Medical Science.2023;[Epub]     CrossRef
  • Who Let the Dogs Out? Unmasking the Neglected: A Semi-Systematic Review on the Enduring Impact of Toxocariasis, a Prevalent Zoonotic Infection
    Katrin Henke, Sotirios Ntovas, Eleni Xourgia, Aristomenis K. Exadaktylos, Jolanta Klukowska-Rötzler, Mairi Ziaka
    International Journal of Environmental Research and Public Health.2023; 20(21): 6972.     CrossRef
  • Eosinophilic leukaemoid reaction and myocardial involvement in a male adolescent with Toxocara canis infection
    Panagiotis Krepis, Nikos Spyridis, Despina N Maritsi, Vasiliki Tsekoura, Lydia Kossiva
    Journal of Paediatrics and Child Health.2021; 57(6): 935.     CrossRef
  • A new ELISA and western blot technique based on recombinant TES antigen and/or larval antigen for the detection of toxocariasis in humans
    Marie-Kristin Raulf, Daniela Jordan, Herbert Auer, Jens M. Warnecke, Bernd Lepenies, Christina Strube
    Parasitology.2021; 148(3): 333.     CrossRef
  • Screening of Cystic Echinococcosis and Toxocariasis in Urmia Municipal Workers, Northwest Iran
    Negar Asadi, Khosrow Hazrati Tappeh, Iraj Mohebbi, Elham Yousefi, Shahram Khademvatan
    Infectious Disorders - Drug Targets.2021; 21(2): 220.     CrossRef
  • A Neurotoxocariasis Case Manifesting Multiple Cerebral Infarction and Eosinophilic Meningoencephalitis
    SangJoon Kang, Jaeyoung Park, Hoe Jong Jeong, Jae-Jeong Joo, Seungmin Kim
    Journal of the Korean Neurological Association.2021; 39(4): 331.     CrossRef
  • Toxocariasis as a Rare Parasitic Complication of a Transthoracic Spine Surgery Procedure
    Jan Soukup, Jan Cerny, Martin Cegan, Petr Kelbich, Tomas Novotny
    Medicina.2021; 57(12): 1328.     CrossRef
  • New insight into the diagnostic cut-off value of serum anti-ToxocaraIgG for ocular toxocariasis in uveitis patients
    N.F. Abd El-Aal, M.A.A. Basha, A.M. Eid
    Journal of Helminthology.2020;[Epub]     CrossRef
  • Seroprevalence of Larval Toxocarosis in the Czech Republic
    Katerina Skulinova, Jan Novak, Martin Kasny, Libuse Kolarova
    Acta Parasitologica.2020; 65(1): 68.     CrossRef
  • Toxocara infection in Italian myelitis
    Beuy Joob, Viroj Wiwanitkit
    Neurological Sciences.2020; 41(4): 973.     CrossRef
  • Establishment of an Experimental Procedure for Preparing Trial Serum Samples for the Specific Serodiagnosis of Toxocara canis for External Quality Assessment Schemes
    Quang Huy Vu, Diep Tuan Tran, Phu Manh Sieu Tran, Van Chuong Le, Thi Diem Phuc Huynh, Quang Sang Bui
    Journal of Parasitology Research.2020; 2020: 1.     CrossRef
  • Prevalence of Toxocariasis and Its Risk Factors in Patients with Eosinophilia in Korea
    Hyun Beom Song, Deokho Lee, Yan Jin, Jinwoo Kang, Shin-Hyeong Cho, Min Sun Park, Jin-Ho Park, Woo-Jung Song, Hye-Ryun Kang, Sang Hyub Lee, Sung-Tae Hong, Min-Ho Choi
    The Korean Journal of Parasitology.2020; 58(4): 413.     CrossRef
  • An innovative approach in the detection of Toxocara canis excretory/secretory antigens using specific nanobodies
    Francisco J. Morales-Yanez, Idalia Sariego, Cécile Vincke, Gholamreza Hassanzadeh-Ghassabeh, Katja Polman, Serge Muyldermans
    International Journal for Parasitology.2019; 49(8): 635.     CrossRef
  • Human toxocariasis – A look at a neglected disease through an epidemiological ‘prism’
    Ali Rostami, Guangxu Ma, Tao Wang, Anson V. Koehler, Andreas Hofmann, Bill C.H. Chang, Calum N. Macpherson, Robin B. Gasser
    Infection, Genetics and Evolution.2019; 74: 104002.     CrossRef
  • Ocular toxocariasis: a neglected parasitic disease in Egypt
    Nagwa Mostafa El-Sayed, Nagham Gamal Masoud
    Bulletin of the National Research Centre.2019;[Epub]     CrossRef
  • Clinical Profile, Treatment, and Visual Outcome of Ocular Toxocara in a Tertiary Eye Care Centre
    Ekta S. Sahu, Bikramjit Pal, Tarun Sharma, Jyotirmay Biswas
    Ocular Immunology and Inflammation.2018; 26(5): 753.     CrossRef
  • Human toxocariasis
    Guangxu Ma, Celia V Holland, Tao Wang, Andreas Hofmann, Chia-Kwung Fan, Rick M Maizels, Peter J Hotez, Robin B Gasser
    The Lancet Infectious Diseases.2018; 18(1): e14.     CrossRef
  • Zoonotic helminth exposure and risk of allergic diseases: A study of two generations in Norway
    N. O. Jõgi, C. Svanes, S. P. Siiak, E. Logan, J. W. Holloway, J. Igland, A. Johannessen, M. Levin, F. G. Real, V. Schlunssen, W. G. C. Horsnell, R. J. Bertelsen
    Clinical & Experimental Allergy.2018; 48(1): 66.     CrossRef
  • Toxocariasis: a silent threat with a progressive public health impact
    Jia Chen, Quan Liu, Guo-Hua Liu, Wen-Bin Zheng, Sung-Jong Hong, Hiromu Sugiyama, Xing-Quan Zhu, Hany M. Elsheikha
    Infectious Diseases of Poverty.2018;[Epub]     CrossRef
  • Detection of Toxocara canis DNA in tissues of experimentally infected mice
    Micaele Quintana de Moura, Marcia Raquel Pegoraro de Macedo, Wesley Douglas da Silva Terto, Luciana Farias da Costa Avila, Fabio Pereira Leivas Leite, Carlos James Scaini, Natália Berne Pinto, Gabriela de Almeida Capella, Adriane Leites Strothmann, Marcos
    Acta Tropica.2018; 187: 51.     CrossRef
  • Comparison of ELISA and Urine Microscopy for Diagnosis ofSchistosoma haematobiumInfection
    Hyun Beom Song, Jiyoung Kim, Yan Jin, Jin Soo Lee, Hoo Gn Jeoung, Young Ha Lee, Abd Al Wahab Saeed, Sung-Tae Hong
    Journal of Korean Medical Science.2018;[Epub]     CrossRef
  • Genetic analysis of Toxocara spp. in stray cats and dogs in Van province, Eastern Turkey
    Bekir Oguz, Nalan Ozdal, M. Serdar Deger
    Journal of Veterinary Research.2018; 62(3): 291.     CrossRef
  • Proteomic analysis of Toxocara canis excretory and secretory (TES) proteins
    Rita Leal Sperotto, Frederico Schmitt Kremer, Maria Elisabeth Aires Berne, Luciana F. Costa de Avila, Luciano da Silva Pinto, Karina Mariante Monteiro, Karin Silva Caumo, Henrique Bunselmeyer Ferreira, Natália Berne, Sibele Borsuk
    Molecular and Biochemical Parasitology.2017; 211: 39.     CrossRef
  • Clinical usefulness of Western blotting and ELISA avidity for the diagnosis of human toxocariasis
    M. Rudzińska, B. Kowalewska, K. Sikorska
    Parasite Immunology.2017;[Epub]     CrossRef
  • The Clinical Characteristics of Ocular Toxocariasis in Jeju Island Using Ultra-wide-field Fundus Photography
    Jong Young Lee, Jin Young Kim, Sang-Yoon Lee, Hye Jin Lee, Jin Ho Jeong, Eun Kyoung Lee
    Journal of the Korean Ophthalmological Society.2017; 58(5): 554.     CrossRef
  • Association between intermediate uveitis and toxocariasis in the Korean population
    Jin-woo Kwon, Yoonseob Sim, Donghyun Jee
    Medicine.2017; 96(5): e5829.     CrossRef
  • Humoral response of mice infected with Toxocara canis following different infection schemes
    Jan Novák, Lucie Panská, Tomáš Macháček, Libuše Kolářová, Petr Horák
    Acta Parasitologica.2017;[Epub]     CrossRef
  • Sero-detection of Toxocara canis infection in human with T.canis recombinant arginine kinase, cathepsin L-1 and TES-26 antigens
    Anju Varghese, Opinder K. Raina, Dinesh Chandra, Bijay R. Mirdha, Naresh H. Kelawala, Jayesh B. Solanki, Niranjan Kumar, Reghu Ravindran, Anandanarayanan Arun, Ajayta Rialch, Hniang Lalrinkima, Rohan N. Kelawala, Subhamoy Samanta
    Acta Parasitologica.2017;[Epub]     CrossRef
  • Evaluation of Toxocara cati Excretory–Secretory Larval Antigens in Serodiagnosis of Human Toxocariasis
    Mohammad Zibaei, Seyed Mahmoud Sadjjadi, Bahador Sarkari, Shoji Uga
    Journal of Clinical Laboratory Analysis.2016; 30(3): 248.     CrossRef
  • Diagnostic Value of the Serum Anti-ToxocaraIgG Titer for Ocular Toxocariasis in Patients with Uveitis at a Tertiary Hospital in Korea
    Ki Woong Bae, Seong Joon Ahn, Kyu Hyung Park, Se Joon Woo
    Korean Journal of Ophthalmology.2016; 30(4): 258.     CrossRef
  • A Case of Subconjunctival Thelasia Callipaeda Infestation
    Young Je Choi, Gwang Rae Shin, Young Duk Kim
    Journal of the Korean Ophthalmological Society.2016; 57(9): 1476.     CrossRef
  • Detection of Specific Antibody Reactivity to Toxocara Larval Excretory-secretory Antigens in Asthmatic Patients (5-15 Years)
    Mahdi Mosayebi, Latif Moini, Reza Hajihossein, Mojtaba Didehdar, Zahra Eslamirad
    The Open Microbiology Journal.2016; 10(1): 162.     CrossRef
  • Cross-reactivity of Toxocariasis with Crude Antigen ofToxascaris leoninaLarvae by ELISA
    Yan Jin, Chenghua Shen, Sun Huh, Min-Ho Choi, Sung-Tae Hong
    Journal of Korean Medical Science.2015; 30(5): 549.     CrossRef
  • Klasyczne i nowoczesne metody diagnozowania toksokarozy u dzieci
    Anna Kroteń, Artur Sulik, Elżbieta Ołdak
    Pediatria Polska.2015; 90(4): 319.     CrossRef
  • Pulmonary Toxocariasis: Initial and Follow-Up CT Findings in 63 Patients
    Kyung Hee Lee, Tae Jung Kim, Kyung Won Lee
    American Journal of Roentgenology.2015; 204(6): 1203.     CrossRef
  • A Case of Eosinophilic Pleural Effusion Caused by Toxocariasis without Serum Eosinophilia
    Min Ji Cho, Ju Ock Kim, Sung Soo Jung, Hee Sun Park, Da Hyun Kang, Dong Il Park
    Soonchunhyang Medical Science.2015; 21(2): 173.     CrossRef
  • SEROPOSITIVITY FOR ASCARIOSIS AND TOXOCARIOSIS AND CYTOKINE EXPRESSION AMONG THE INDIGENOUS PEOPLE IN THE VENEZUELAN DELTA REGION
    Zaida Araujo, Sietze Brandes, Elena Pinelli, María A. Bochichio, Andrea Palacios, Albina Wide, Bruno Rivas-Santiago, Juan Carlos Jiménez
    Revista do Instituto de Medicina Tropical de São Paulo.2015; 57(1): 47.     CrossRef
  • Significance of Serum Antibody Test for Toxocariasis in Healthy Healthcare Examinees with Eosinophilia in Seoul and Gyeongsangnam-do, Korea
    Hong Seok Kim, Yan Jin, Min-Ho Choi, Jae-Hwan Kim, Young Ha Lee, Cheong Ha Yoon, Eui-Hyuk Hwang, Hun Kang, Sang-Yong Ahn, Gi Jin Kim, Sung-Tae Hong
    Journal of Korean Medical Science.2014; 29(12): 1618.     CrossRef
  • Ocular toxocariasis: clinical features, diagnosis, treatment, and prevention
    Seong Joon Ahn, Na-Kyung Ryoo, Se Joon Woo
    Asia Pacific Allergy.2014; 4(3): 134.     CrossRef
  • Human toxocariasis: current advances in diagnostics, treatment, and interventions
    Gustavo Marçal Schmidt Garcia Moreira, Paula de Lima Telmo, Marcelo Mendonça, Ângela Nunes Moreira, Alan John Alexander McBride, Carlos James Scaini, Fabricio Rochedo Conceição
    Trends in Parasitology.2014; 30(9): 456.     CrossRef
  • Toxocara Optic Neuropathy after Ingestion of Raw Meat Products
    Hee Kyung Yang, Se Joon Woo, Jeong-Min Hwang
    Optometry and Vision Science.2014; 91(11): e267.     CrossRef
  • Clinical Features and Course of Ocular Toxocariasis in Adults
    Seong Joon Ahn, Se Joon Woo, Yan Jin, Yoon-Seok Chang, Tae Wan Kim, Jeeyun Ahn, Jang Won Heo, Hyeong Gon Yu, Hum Chung, Kyu Hyung Park, Sung Tae Hong, Calum N. L. Macpherson
    PLoS Neglected Tropical Diseases.2014; 8(6): e2938.     CrossRef
  • 12,726 View
  • 163 Download
  • Crossref

Mini Review

Clinical Features and Treatment of Ocular Toxoplasmosis
Young-Hoon Park, Ho-Woo Nam
Korean J Parasitol 2013;51(4):393-399.
Published online August 30, 2013
DOI: https://doi.org/10.3347/kjp.2013.51.4.393

Ocular toxoplasmosis is a disease caused by the infection with Toxoplasma gondii through congenital or acquired routes. Once the parasite reaches the retina, it proliferates within host cells followed by rupture of the host cells and invasion into neighboring cells to make primary lesions. Sometimes the restricted parasite by the host immunity in the first scar is activated to infect another lesion nearby the scar. Blurred vision is the main complaint of ocular toxoplasmic patients and can be diagnosed by detection of antibodies or parasite DNA. Ocular toxoplasmosis needs therapy with several combinations of drugs to eliminate the parasite and accompanying inflammation; if not treated it sometimes leads to loss of vision. We describe here clinical features and currently available chemotherapy of ocular toxoplasmosis.

Citations

Citations to this article as recorded by  Crossref logo
  • Systematic screening identifies medication and disease factors associated with schizophrenia risk
    Ariel Israel, Abraham Weizman, Sarah Israel, Joshua Stokar, Shai Ashkenazi, Shlomo Vinker, Eli Magen, Eugene Merzon
    Brain, Behavior, and Immunity.2026; 131: 106135.     CrossRef
  • The importance of translational research in the study of ocular toxoplasmosis: insights from the 17th International Congress on Toxoplasmosis 2024
    Alejandra de-la-Torre, Germán Mejía-Salgado, Gereon Schares
    FEMS Microbes.2025;[Epub]     CrossRef
  • A COMBINATION REGIMEN OF INTRAVITREAL CLINDAMYCIN WITH DEXAMETHASONE, SYSTEMIC CO-TRIMOXAZOLE AND STEROIDS FOR MACULAR TOXOPLASMA RETINOCHOROIDITIS IN IMMUNOCOMPETENT CASES
    Sushree Satavasia, Akshay Mishra, Vishal Jadhav, Talluri Ronnie Abhishek, Anup Kelgaonkar, Anamika Patel, Soumyava Basu, Avinash Pathengay
    Retina.2025; 45(5): 871.     CrossRef
  • Deep Learning-Based Classification of Ocular Toxoplasmosis Fundus Images: A Comparative Study of CNN and SVM Models
    Shivam Tiwari, Kalicharan Sahu, Surbhi Vijh, Charu Awasthi
    Procedia Computer Science.2025; 259: 1189.     CrossRef
  • Epidemiological spectrum of infectious uveitis in the Asia-Pacific
    Alexander Newman, Peter McCluskey
    Taiwan Journal of Ophthalmology.2025; 15(2): 157.     CrossRef
  • Toxoplasmosis in patient underwent stem cell transplantation, bone marrow transplantation due to multiple myeloma
    Magdalena Bulek, Aleksandra Kopyś-Wócik, Natalie Papachristoforou, Aleksandra Kocjan
    Postępy Higieny i Medycyny Doświadczalnej.2025; 79(1): 106.     CrossRef
  • Toxoplasma gondii at the Host Interface: Immune Modulation and Translational Strategies for Infection Control
    Billy J. Erazo Flores, Laura J. Knoll
    Vaccines.2025; 13(8): 819.     CrossRef
  • A Comprehensive Review of Toxoplasmosis: Serious Threat to Human Health
    Aswin Rafif Khairullah, Shendy Canadya Kurniawan, Agus Widodo, Mustofa Helmi Effendi, Abdullah Hasib, Otto Sahat Martua Silaen, Sancaka Chasyer Ramandinianto, Ikechukwu Benjamin Moses, Katty Hendriana Priscilia Riwu, Sheila Marty Yanestria, Muhammad Esa E
    The Open Public Health Journal.2024;[Epub]     CrossRef
  • Benchmarking Deep Learning Frameworks for Automated Diagnosis of Ocular Toxoplasmosis: A Comprehensive Approach to Classification and Segmentation
    Syed Samiul Alam, Samiul Based Shuvo, Shams Nafisa Ali, Fardeen Ahmed, Arbil Chakma, Yeong Min Jang
    IEEE Access.2024; 12: 22759.     CrossRef
  • From Misdiagnosis to Management: A Case Report of Ocular Inflammatory Disease
    Catarina M Francisco, Miguel Santos, Sofia Mano, Inês Leal, Joana Coelho
    Cureus.2024;[Epub]     CrossRef
  • Posterior segment optical coherence tomography: A diagnostic aid in posterior uveitis
    Parul M. Danayak, Rupal M. Chaudhary, Zalak Shah
    Kerala Journal of Ophthalmology.2024; 36(2): 152.     CrossRef
  • Human Ocular Toxoplasmosis in Romania: History, Epidemiology, and Public Health: A Narrative Review
    Laura Andreea Ghenciu, Ovidiu Alin Hațegan, Sorin Lucian Bolintineanu, Alexandra-Ioana Dănilă, Roxana Iacob, Emil Robert Stoicescu, Maria Alina Lupu, Tudor Rareș Olariu
    Microorganisms.2024; 12(8): 1541.     CrossRef
  • Ocular Toxoplasmosis
    Eunice Jin Hui Goh, Ikhwanuliman Putera, Rina La Distia Nora, Padmamalini Mahendradas, Jyotirmay Biswas, Soon-Phaik Chee, Ilaria Testi, Carlos E Pavesio, Andre Luiz Land Curi, Daniel Vitor Vasconcelos-Santos, Atul Arora, Vishali Gupta, Alejandra de-la-Tor
    Ocular Immunology and Inflammation.2023; 31(7): 1342.     CrossRef
  • Etiology of Pediatric Uveitis in a Tertiary Pediatric Eye Hospital in Egypt
    Eiman Abd El Latif, Rasha Mousa, Mohammed Tawfeeq Mahdi, Ahmed Mahmoud Amin, Mahmoud Mohammed Ahmed Ali, Nour Eldin Abdelhamid, Mohamed Elmoddather, Hassan Shamselden Yousef, Ehab Hafez Gouda Hafez, Sameh Galal Taher Salem, Ashraf Hassan Soliman
    Ocular Immunology and Inflammation.2023; 31(10): 1978.     CrossRef
  • Interferon-gamma release assay and chest X-ray to classify intraocular tuberculosis among clinically undifferentiated uveitis
    Mei Riasanti, Ikhwanuliman Putera, Priscilla Jessica, Muhammad Zakiy Waliyuddin, Faiz Alwan Tagar, Andini Karlina CH, Yulia Aziza, Made Susiyanti, Lukman Edwar, Ratna Sitompul, Rina La Distia Nora
    Medical Journal of Indonesia.2023; 31(4): 225.     CrossRef
  • Stepwise approach for fundus imaging in the diagnosis and management of posterior uveitis
    Aniruddha Agarwal, Francesco Pichi, Alessandro Invernizzi, Dilraj S. Grewal, Rohan Bir Singh, Awaneesh Upadhyay
    Survey of Ophthalmology.2023; 68(3): 446.     CrossRef
  • Macular Pucker: A Devastating Complication in Ocular Toxoplasmosis
    Syarifah Nur Humaira Syed Mohd Khomsah, Julieana Muhammed, Wan-Hazabbah Wan Hitam
    Cureus.2023;[Epub]     CrossRef
  • Optical Coherence Tomography Angiography of the Choriocapillaris in Subclinical Toxoplasma Chorioretinitis: A Case Report
    Ahmed B Alsatrawi
    Cureus.2023;[Epub]     CrossRef
  • Retinal ferroptosis as a critical mechanism for the induction of retinochoroiditis during ocular toxoplasmosis
    Kazuhisa Yamada, Akira Tazaki, Nanako Ushio-Watanabe, Yoshihiko Usui, Atsunobu Takeda, Masaaki Matsunaga, Ayana Suzumura, Hideyuki Shimizu, Hao Zheng, Nanang R. Ariefta, Masahiro Yamamoto, Hideaki Hara, Hiroshi Goto, Koh-Hei Sonoda, Koji M. Nishiguchi, Ma
    Redox Biology.2023; 67: 102890.     CrossRef
  • Pediatric Posterior Infectious Uveitis
    André Luiz Land Curi, Alejandra de-la-Torre, Ariel Schlaen, Papdmamalini Mahendradas, Jyortimay Biswas
    Ocular Immunology and Inflammation.2023; 31(10): 1944.     CrossRef
  • Toxoplasmosis Related Neuroretinitis: More than Meets the Eye
    Alastair Coulson, Divya Jacob, Lyudmila Kishikova, Ahmed Saad
    Ocular Immunology and Inflammation.2022; 30(3): 556.     CrossRef
  • Utility of blood as the clinical specimen for the diagnosis of ocular toxoplasmosis using uracil DNA glycosylase-supplemented loop-mediated isothermal amplification and real-time polymerase chain reaction assays based on REP-529 sequence and B1 gene
    Bahman Rahimi Esboei, Shirzad Fallahi, Mohammad Zarei, Bahram Kazemi, Mehdi Mohebali, Saeedeh Shojaee, Parisa Mousavi, Aref Teimouri, Raziyeh Mahmoudzadeh, Mirataollah Salabati, Hossein Keshavarz Valian
    BMC Infectious Diseases.2022;[Epub]     CrossRef
  • Toxoplasma Chorioretinitis
    Somya Ish, Shreyash Agrawal, Pranav Ish
    Indian Journal of Medical Specialities.2022; 13(1): 67.     CrossRef
  • Ocular Toxoplasmosis: A Review of Current Literature
    Neal S. Patel, Demetrios G. Vavvas
    International Ophthalmology Clinics.2022; 62(2): 231.     CrossRef
  • Calomys callosus: An Experimental Animal Model Applied to Parasitic Diseases Investigations of Public Health Concern
    Rafael Borges Rosa, Mylla Spirandelli da Costa, Samuel Cota Teixeira, Emilene Ferreira de Castro, Willyenne Marília Dantas, Eloisa Amália Vieira Ferro, Murilo Vieira da Silva
    Pathogens.2022; 11(3): 369.     CrossRef
  • Insights From the Eye for Patients With Kidney Transplant
    Christine Xu, Alisa J. Prager, Carolyn D. Alonso, Aditya S. Pawar
    Transplantation Proceedings.2022; 54(8): 2182.     CrossRef
  • An illustration of ocular toxoplasmosis with consequent lenticular opacities and asteroid hyalosis
    Dimakatso G. Mashala
    African Vision and Eye Health.2022;[Epub]     CrossRef
  • Azithromycin concentration in rabbits’ plasma and posterior segment of the eyes following oral drug administration: a dose-finding study for the application in ocular toxoplasmosis
    Hisar Daniel, Melva Louisa, Lukman Edwar
    Journal of Pharmacy and Pharmacology.2022; 74(12): 1743.     CrossRef
  • Revenge of the Tick: Tick-Borne Diseases and the Eye in the Age of Climate Change and Globalisation
    Xin Le Ng, Berdjette Y. Y. Lau, Cassandra X. C. Chan, Dawn K. A. Lim, Blanche X. H. Lim, Chris H. L. Lim
    Zoonotic Diseases.2022; 2(4): 183.     CrossRef
  • Infectious Sclerouveitis in an Immunocompetent Patient: A Probable Case of Simultaneous Ocular Tuberculosis and Toxoplasmosis
    Wen K Chong, Karen Khoo Kah Kuen, Lam Mun-Wei, Abdul-Salim Ismail, Azhany Yaakub
    Cureus.2022;[Epub]     CrossRef
  • Insights from the Eye for Patients with Kidney Transplant
    Christine Xu, Alisa J. Prager, Carolyn D. Alonso, Aditya Pawar
    SSRN Electronic Journal.2022;[Epub]     CrossRef
  • Ocular toxoplasmosis: phenotype differences between toxoplasma IgM positive and IgM negative patients in a large cohort
    Sofia Ajamil-Rodanes, Joshua Luis, Rabia Bourkiza, Benedict Girling, Angela Rees, Catherine Cosgrove, Carlos Pavesio, Mark Westcott
    British Journal of Ophthalmology.2021; 105(2): 210.     CrossRef
  • Retinal vasculitis: A framework and proposal for a classification system
    Ghazala A. Datoo O'Keefe, Narsing Rao
    Survey of Ophthalmology.2021; 66(1): 54.     CrossRef
  • Retinocoroiditis toxoplásmica de presentación atípica en pacientes con enfermedades hematológicas malignas
    J.P. Figueroa-Vercellino, L. Miguel, A. Moll-Udina, C. Alba-Linero, V. Llorenç, A. Adán
    Archivos de la Sociedad Española de Oftalmología.2021; 96(3): 152.     CrossRef
  • Atypical toxoplasmic retinochoroiditis in patients with malignant hematological diseases
    J.P. Figueroa-Vercellino, L. Miguel, A. Moll-Udina, C. Alba-Linero, V. Llorenç, A. Adán
    Archivos de la Sociedad Española de Oftalmología (English Edition).2021; 96(3): 152.     CrossRef
  • Detection of antibodies to Toxoplasma gondii among owned dogs in Cambodia
    Thi Thuy Nguyen, Chanya Kengradomkij, Tawin Inpankaew
    Food and Waterborne Parasitology.2021; 22: e00103.     CrossRef
  • Etiology of Uveitis in Upper Egypt
    Eiman Abd El Latif, Asaad Nooreldin, Mohammed Shikhoun Ahmed, Mohamed Elmoddather, Wael El Gendy
    Clinical Ophthalmology.2021; Volume 15: 195.     CrossRef
  • Screening for common eye diseases in the elderly with Optos ultra-wide-field scanning laser ophthalmoscopy: a pilot study with focus on ocular toxoplasmosis
    Pablo Eduardo Logroño Wiese, Frank Seeber, Anne-Sophie Endres, Claudia Brockmann, Uwe Pleyer
    International Ophthalmology.2021; 41(5): 1573.     CrossRef
  • Ocular Toxoplasmosis: Mechanisms of Retinal Infection and Experimental Models
    Veronica Rodriguez Fernandez, Giovanni Casini, Fabrizio Bruschi
    Parasitologia.2021; 1(2): 50.     CrossRef
  • Acquired Immunodeficiency Syndrome Presented as Atypical Ocular Toxoplasmosis
    Elias Khalili Pour, Hamid Riazi-Esfahani, Nazanin Ebrahimiadib, Violet Zaker Esteghamati, Mohammad Zarei, Kamal Kishore
    Case Reports in Ophthalmological Medicine.2021; 2021: 1.     CrossRef
  • The challenges of treating a patient with recurrent congenital toxoplasmic chorioretinitis
    Aleksandra Krasińska, Kamila Jaz, Joanna Mamczur, Jarosław Kocięcki
    Medical Journal of Cell Biology.2021; 9(2): 56.     CrossRef
  • A Trust-Based Methodology to Evaluate Deep Learning Models for Automatic Diagnosis of Ocular Toxoplasmosis from Fundus Images
    Rodrigo Parra, Verena Ojeda, Jose Luis Vázquez Noguera, Miguel García-Torres, Julio César Mello-Román, Cynthia Villalba, Jacques Facon, Federico Divina, Olivia Cardozo, Verónica Elisa Castillo, Ingrid Castro Matto
    Diagnostics.2021; 11(11): 1951.     CrossRef
  • The pathogenicity and virulence of Toxoplasma gondii
    Syrian G. Sanchez, Sébastien Besteiro
    Virulence.2021; 12(1): 3095.     CrossRef
  • Toxoplasma Retinochoroiditis with Chorioretinal Neovascularization in a Young Patient
    Nikhila S. Khandwala, Robert A. Hyde, Cagri G. Besirli
    Case Reports in Ophthalmology.2021; 12(1): 259.     CrossRef
  • The Diagnostic Conundrum of Retinitis and a Pigmented Scar
    Nikhila S. Khandwala, Jason M.L. Miller, Robert A. Hyde, Christopher D. Conrady, Rajesh C. Rao, Cagri G. Besirli
    Case Reports in Ophthalmology.2021; 12(1): 164.     CrossRef
  • OCULAR TOXOPLASMOSIS
    Iskren Kaftandjiev, Rumen Harizanov
    PROBLEMS of Infectious and Parasitic Diseases.2021; 49(1): 41.     CrossRef
  • TRATAMENTOS ALTERNATIVOS PARA TOXOPLASMOSE OCULAR: uma revisão integrativa
    Patricia Emanuella Ramos Marzola, Rodrigo Vasconcelos Marzola
    Arquivos Catarinenses de Medicina.2021; 49(4): 98.     CrossRef
  • Effectiveness of Treatments for Ocular Toxoplasmosis
    Julio Casoy, Heloisa Nascimento, Luci Meire P. Silva, Yuslay Fernández-Zamora, Cristina Muccioli, João Rafael de Oliveira Dias, Mário Junqueira Nóbrega, Heloísa Amaral Junqueira Nóbrega, Jacqueline Zummo, Rubens Belfort
    Ocular Immunology and Inflammation.2020; 28(2): 249.     CrossRef
  • Chorio-retinal toxoplasmosis: treatment outcomes, lesion evolution and long-term follow-up in a single tertiary center
    Vicktoria Vishnevskia-Dai, Asaf Achiron, Ortal Buhbut, Ofri Vorobichik Berar, Anne Ampaire Musika, Sivan M. Elyashiv, Idan Hecht
    International Ophthalmology.2020; 40(4): 811.     CrossRef
  • Toxoplasma gondii Parasitophorous Vacuole Membrane-Associated Dense Granule Proteins Regulate Maturation of the Cyst Wall
    Rebekah B. Guevara, Barbara A. Fox, David J. Bzik, Silvia N. J. Moreno
    mSphere.2020;[Epub]     CrossRef
  • Optical coherence tomography angiography findings in macular toxoplasma retinochoroiditis: A case report
    Alejandro L. Perez, Rosa A. Lozada, Andres Emanuelli, Armando L. Oliver
    American Journal of Ophthalmology Case Reports.2020; 19: 100764.     CrossRef
  • New findings useful for clinical practice using swept-source optical coherence tomography angiography in the follow-up of active ocular toxoplasmosis
    João Rafael de Oliveira Dias, Camila Campelo, Eduardo Amorim Novais, Gabriel Costa de Andrade, Paula Marinho, Yusláy Fernández Zamora, Luciana Finamor Peixoto, Maurício Maia, Heloísa Nascimento, Rubens Belfort
    International Journal of Retina and Vitreous.2020;[Epub]     CrossRef
  • Optical Coherence Tomography Angiography Analysis of Retinal and Choroidal Vascular Networks during Acute, Relapsing, and Quiescent Stages of Macular Toxoplasma Retinochoroiditis
    Georges Azar, Catherine Favard, Sawsen Salah, Antoine Brézin, Vivien Vasseur, Martine Mauget-Faÿsse, Luca Di Antonio
    BioMed Research International.2020;[Epub]     CrossRef
  • Dual-Stage Picolinic Acid-Derived Inhibitors of Toxoplasma gondii
    Muhammad M. Khalifa, Bruno Martorelli Di Genova, Sarah G. McAlpine, Gina M. Gallego-Lopez, David M. Stevenson, Soren D. Rozema, Neil P. Monaghan, James C. Morris, Laura J. Knoll, Jennifer E. Golden
    ACS Medicinal Chemistry Letters.2020; 11(12): 2382.     CrossRef
  • TOXOPLASMA NEURO-RETINITIS IN AN IMMUNO-COMPETENT ADULT- A CASE REPORT AND REVIEW OF LITERATURE
    Tharini Senthamizh, Subashini Kaliaperumal
    INTERNATIONAL JOURNAL OF SCIENTIFIC RESEARCH.2020; : 1.     CrossRef
  • Bilateral Ocular Toxoplasmosis that Caused Optic Atrophy Secondary to Papillitis
    Donghun Lee, Minwoo Kim, Jong Won Moon
    Journal of the Korean Ophthalmological Society.2020; 61(9): 1109.     CrossRef
  • A white circular-spot pattern of iridian atrophy associated with Varicella-zoster virus and Toxoplasma gondii coinfection: a case report
    Juliana Muñoz-Ortiz, Olga Lorena Rubio-Romero, Maria Cecilia Cedeño, Karla Arteaga-Rivera, Alejandra de-la-Torre
    BMC Ophthalmology.2020;[Epub]     CrossRef
  • Dipenyleneiodonium Induces Growth Inhibition of Toxoplasma gondii through ROS Induction in ARPE-19 Cells
    Pu Reum Sun, Fei Fei Gao, Hei Gwon Choi, Wei Zhou, Jae-Min Yuk, Jaeyul Kwon, Young-Ha Lee, Guang-Ho Cha
    The Korean Journal of Parasitology.2019; 57(2): 83.     CrossRef
  • Management of Advanced HIV Disease
    Nathan A. Summers, Wendy S. Armstrong
    Infectious Disease Clinics of North America.2019; 33(3): 743.     CrossRef
  • Profil clinique et épidémiologique de la toxoplasmose oculaire à Kinshasa
    N. Nsiangani Lusambo, D. Kaimbo Wa Kaimbo
    Journal Français d'Ophtalmologie.2019; 42(8): 900.     CrossRef
  • Electrochemiluminescence Epidemiologic Detection of Toxoplasma gondii Infection in Pregnant Women With Direct and Indirect Diagnostic Techniques (ELISA Avidity Plus Biochemical Assay), Tehran, Iran
    Ehsan Shariat Bahadory, Ali Dalir Ghaffari, Somayyeh Namrood, Seyyedeh Somayyeh Mosavipour, Javid Sadraie
    International Journal of Epidemiologic Research.2019; 6(2): 49.     CrossRef
  • Status of common parasitic diseases in Korea in 2019
    Sun Huh
    Journal of the Korean Medical Association.2019; 62(8): 437.     CrossRef
  • Fulminant Toxoplasmic Chorioretinitis Following Intravitreal Dexamethasone Implantation
    Areum Jeong, Dong-Geun Park, Min Sagong
    Journal of the Korean Ophthalmological Society.2019; 60(9): 896.     CrossRef
  • The Eye as a Window to Systemic Infectious Diseases: Old Enemies, New Imaging
    Vittorio Pirani, Paolo Pelliccioni, Serena De Turris, Alessandro Rosati, Alessandro Franceschi, Claudia Cesari, Michele Nicolai, Cesare Mariotti
    Journal of Clinical Medicine.2019; 8(9): 1392.     CrossRef
  • Association of TREM-1, IL-1β, IL-33/ST2, and TLR Expressions With the Pathogenesis of Ocular Toxoplasmosis in Mouse Models on Different Genetic Backgrounds
    Yanxia Zhang, Jian He, Huanqin Zheng, Shiguang Huang, Fangli Lu
    Frontiers in Microbiology.2019;[Epub]     CrossRef
  • Toxoplasma gondii Intravacuolar-Network-Associated Dense Granule Proteins Regulate Maturation of the Cyst Matrix and Cyst Wall
    Rebekah B. Guevara, Barbara A. Fox, Alejandra Falla, David J. Bzik, Silvia N. J. Moreno
    mSphere.2019;[Epub]     CrossRef
  • Ocular toxoplasmosis with surprisingly good retinal function
    Tove Lise Morisbakk, Per O Lundmark
    Scandinavian Journal of Optometry and Visual Science.2019; 12(1): 1.     CrossRef
  • Water related ocular diseases
    Syed Shoeb Ahmad
    Saudi Journal of Ophthalmology.2018; 32(3): 227.     CrossRef
  • Assessment of ocular toxoplasmosis patients reported at a tertiary center in the northeast of Iran
    Seyedeh Maryam Hosseini, Elham Moghaddas, Karim Sharifi, Malihe Dadgar Moghaddam, Seyed Aliakbar Shamsian
    International Ophthalmology.2018; 38(6): 2527.     CrossRef
  • Ocular Toxoplasmosis Mimicking Choroidal Metastasis From Colorectal Adenocarcinoma
    Samuel C. Fowler, Daniel R. Capiz-Correa, Hans E. Grossniklaus, Rebecca D. Shadowen, David A. Reichstein
    Journal of VitreoRetinal Diseases.2018; 2(6): 384.     CrossRef
  • A Perspective on Thiazolidinone Scaffold Development as a New Therapeutic Strategy for Toxoplasmosis
    Cristian Rocha-Roa, Diego Molina, Néstor Cardona
    Frontiers in Cellular and Infection Microbiology.2018;[Epub]     CrossRef
  • Diagnostic and Therapeutic Challenges
    Quraish Ghadiali, Orly Gal-Or, Jonathan Naysan, James Klancnik, K. Bailey Freund, SriniVas R. Sadda
    Retina.2018; 38(12): 2429.     CrossRef
  • Swept-source optical coherence tomography and optical coherence tomography angiography in acquired toxoplasmic chorioretinitis: a case report
    Diego Vezzola, Davide Allegrini, Alfredo Borgia, Paolo Fogagnolo, Luca Mario Rossetti, Mario R. Romano, Stefano De Cillà
    Journal of Medical Case Reports.2018;[Epub]     CrossRef
  • Analysis Concentration of <i>Toxoplasma gondii</i> on Anti-Toxoplasma IgG-IgM Antibody Levels, and the Outcomes of Pregnancy in Mice Balb/c
    Tigor Peniel Simanjuntak, Mochammad Hatta, Robert H. Sirait, Marni Br Karo, Lenny Irmawaty Sirait, Tetty Rina Aritonang, Syahrul Rauf, Ressy Dwiyanti
    Open Journal of Obstetrics and Gynecology.2017; 07(03): 281.     CrossRef
  • Recent Developments in the Diagnosis and Treatment of Ocular Toxoplasmosis
    Cem Ozgonul, Cagri Giray Besirli
    Ophthalmic Research.2017; 57(1): 1.     CrossRef
  • Infectious uveitis: An enigma
    Parthopratim Dutta Majumder, Avirupa Ghosh, Jyotirmay Biswas
    Middle East African Journal of Ophthalmology.2017; 24(1): 2.     CrossRef
  • Effect of Nigella sativa oil on experimental toxoplasmosis
    Rasha F. Mady, Wessam El-Hadidy, Samar Elachy
    Parasitology Research.2016; 115(1): 379.     CrossRef
  • Host and Toxoplasma gondii genetic and non-genetic factors influencing the development of ocular toxoplasmosis: A systematic review
    Carolina Fernández, Jesús Jaimes, María Camila Ortiz, Juan David Ramírez
    Infection, Genetics and Evolution.2016; 44: 199.     CrossRef
  • Ocular Inflammation Associated with Systemic Infection
    Byung Gil Moon, Joo Yong Lee
    Hanyang Medical Reviews.2016; 36(3): 192.     CrossRef
  • DNA Microarray Detection of 18 Important Human Blood Protozoan Species
    Mu-Xin Chen, Lin Ai, Jun-Hu Chen, Xin-Yu Feng, Shao-Hong Chen, Yu-Chun Cai, Yan Lu, Xiao-Nong Zhou, Jia-Xu Chen, Wei Hu, Enock Matovu
    PLOS Neglected Tropical Diseases.2016; 10(12): e0005160.     CrossRef
  • Macular infarction in a patient with Toxoplasma retinochoroditis
    Vinod Kumar, Brijesh Takkar, Parijat Chandra, Atul Kumar
    BMJ Case Reports.2016; 2016: bcr2015212596.     CrossRef
  • Müller cell activation and photoreceptor depletion in a mice model of congenital ocular toxoplasmosis
    Ibtissem Lahmar, Alexander W. Pfaff, Luc Marcellin, Arnaud Sauer, Adnane Moussa, Hamouda Babba, Ermanno Candolfi
    Experimental Parasitology.2014; 144: 22.     CrossRef
  • Neuropsychiatric manifestations of latent toxoplasmosis on mothers and their offspring
    Amir Abdoli, Abdolhossein Dalimi, Mohsen Arbabi, Fatemeh Ghaffarifar
    The Journal of Maternal-Fetal & Neonatal Medicine.2014; 27(13): 1368.     CrossRef
  • Excretory–secretory antigens: A suitable candidate for immunization against ocular toxoplasmosis in a murine model
    Kiumars Norouzpour Deilami, Ahmad Daryani, Ehsan Ahmadpour, Mehdi Sharif, Yousef Dadimoghaddam, Shahabeddin Sarvi, Ahad Alizadeh
    Comparative Immunology, Microbiology and Infectious Diseases.2014; 37(5-6): 369.     CrossRef
  • 20,863 View
  • 340 Download
  • Crossref

Original Article

Serodiagnosis of Echinococcosis by ELISA Using Cystic Fluid from Uzbekistan Sheep
Yan Jin, Khikmat Anvarov, Abdukhakim Khajibaev, Samin Hong, Sung-Tae Hong
Korean J Parasitol 2013;51(3):313-317.
Published online June 30, 2013
DOI: https://doi.org/10.3347/kjp.2013.51.3.313

According to increase of travel, the cases of imported echinococcosis have been increasing in Korea. The present study was undertaken to develop a serodiagnostic system for echinococcosis in Korea. For diagnosis of echinococcosis, the fluid of Echinococcus granulosus hydatid cysts was collected from naturally infected sheep in Uzbekistan. Also serum samples of infected patients who were surgically confirmed were collected in a hospital in Tashkent, Uzbekistan. According to the absorbance of 59 echinococcosis positive and 39 negative control serum samples, the cut-off value was determined as 0.27. The sensitivity and specificity of ELISA with hydatid fluid antigen were 91.5% and 96%, respectively. The antigen cross-reacted with the serum of some cysticercosis or clonorchiasis patients. However, immunoblot analysis on the cystic fluid recognized antigenic proteins of 7-, 16-, and 24-kDa bands in their dominant protein quantity and strong blotting reactivity. In conclusion, the present ELISA system using hydatid cyst fluid antigen from Uzbekistan sheep is sensitive and specific for diagnosis of echinococcosis cases.

Citations

Citations to this article as recorded by  Crossref logo
  • Delayed Diagnosis of Imported Cystic Echinococcosis and Successful Treatment With Percutaneous Drainage and Albendazole in Korea: A Case Report
    Won Jun Choi, Hanna Jin, Hyeon Jae Jo, Chan Mi Lee, Chang Kyung Kang, Pyoeng Gyun Choe, Wan Beom Park, Nam Joong Kim, Min-Ho Choi
    Journal of Korean Medical Science.2025;[Epub]     CrossRef
  • Human and camel cystic echinococcosis – a polyclonal antibody-based sandwich ELISA for its serodiagnosis with molecular identification
    A. Maher, N. I. Toaleb, R. M. Shaapan, D. Aboelsoued, M. B. Salman, S. Zaky
    Veterinary Research Communications.2024; 48(4): 2193.     CrossRef
  • Past and present of diagnosis of echinococcosis: A review (1999–2021)
    Mughees Aizaz Alvi, Rana Muhammad Athar Ali, Sadiq Khan, Muhammad Saqib, Warda Qamar, Li Li, Bao-Quan Fu, Hong-Bin Yan, Wan-Zhong Jia
    Acta Tropica.2023; 243: 106925.     CrossRef
  • A Novel Designed Sandwich ELISA for the Detection of Echinococcus granulosus Antigen in Camels for Diagnosis of Cystic Echinococcosis
    Nagwa I. Toaleb, Dina Aboelsoued, Kadria N. Abdel Megeed, Sahar Hussein Abdalla Hekal
    Tropical Medicine and Infectious Disease.2023; 8(8): 400.     CrossRef
  • A simple and efficient purification method of native immunoreactive antigen for diagnosis of camel hydatidosis
    Nagwa I. Toaleb, Mohamed S. Helmy, Eman E. El Shanawany, Eman H. Abdel-Rahman
    Veterinary World.2020; 13(1): 141.     CrossRef
  • Multi-Epitope Fusion Protein Eg mefAg-1 as a Serodiagnostic Candidate for Cystic Echinococcosis in Sheep
    Liu Tianli, Wang Xifeng, Tian Zhenzhong, Wang Lixia, Zhang Xingxing, Qiao Jun, Meng Qingling, Gong Shasha, Chen Ying, Cai Xuepeng
    The Korean Journal of Parasitology.2019; 57(1): 61.     CrossRef
  • An Imported Case of Disseminated Echinococcosis in Korea
    Dong Hoon Shin, Hae Chan Jo, Jeong-Han Kim, Kang Il Jun, Wan Beom Park, Nam-Joong Kim, Min-Ho Choi, Chang Kyung Kang, Myoung-don Oh
    The Korean Journal of Parasitology.2019; 57(4): 429.     CrossRef
  • Serological diagnosis of cystic echinococcosis in cattle
    Aitbay K. Bulashev, Zhanbolat A. Suranshiev, Orken S. Akibekov, Zhanara Zh. Akanova, Gulmira A. Abulgazimova
    Folia Parasitologica.2017;[Epub]     CrossRef
  • Diagnostic value of semi-purified antigens of hydatid cyst fluid in human cystic echinococcosis
    Wissal Iraqi
    Acta Parasitologica.2016;[Epub]     CrossRef
  • Presumptive case of sparganosis manifesting as a hepatic mass: A case report and literature review
    Gyeong Deok Jo, Jae Young Lee, Sung-Tae Hong, Jung Hoon Kim, Joon Koo Han
    World Journal of Radiology.2016; 8(10): 846.     CrossRef
  • Prevalence of Serum IgG Antibodies to Cystic <i>Echinococcus</i> Antigen among Patients in an Uzbekistan Emergency Hospital
    Se Jin Park, Sung Sik Han, Khikmat Anvarov, Abdukhakim Khajibaev, Min-Ho Choi, Sung-Tae Hong
    The Korean Journal of Parasitology.2015; 53(6): 699.     CrossRef
  • Infection Status of Hydatid Cysts in Humans and Sheep in Uzbekistan
    Sung-Tae Hong, Yan Jin, Khikmat Anvarov, Abdukhakim Khadjibaev, Samin Hong, Yusufjon Ahmedov, Utkir Otaboev
    The Korean Journal of Parasitology.2013; 51(3): 383.     CrossRef
  • 9,057 View
  • 124 Download
  • Crossref

Articles from Symposium on Asian Taenia (October 2011, Osong, Korea)

Molecular Approaches to Taenia asiatica
Hyeong-Kyu Jeon, Keeseon S. Eom
Korean J Parasitol 2013;51(1):1-8.
Published online February 18, 2013
DOI: https://doi.org/10.3347/kjp.2013.51.1.1

Taenia solium, T. saginata, and T. asiatica are taeniid tapeworms that cause taeniasis in humans and cysticercosis in intermediate host animals. Taeniases remain an important public health concerns in the world. Molecular diagnostic methods using PCR assays have been developed for rapid and accurate detection of human infecting taeniid tapeworms, including the use of sequence-specific DNA probes, PCR-RFLP, and multiplex PCR. More recently, DNA diagnosis using PCR based on histopathological specimens such as 10% formalin-fixed paraffin-embedded and stained sections mounted on slides has been applied to cestode infections. The mitochondrial gene sequence is believed to be a very useful molecular marker for not only studying evolutionary relationships among distantly related taxa, but also for investigating the phylo-biogeography of closely related species. The complete sequence of the human Taenia tapeworms mitochondrial genomes were determined, and its organization and structure were compared to other human-tropic Taenia tapeworms for which complete mitochondrial sequence data were available. The multiplex PCR assay with the Ta4978F, Ts5058F, Tso7421F, and Rev7915 primers will be useful for differential diagnosis, molecular characterization, and epidemiological surveys of human Taenia tapeworms.

Citations

Citations to this article as recorded by  Crossref logo
  • Identification and functional characterization of the siRNA pathway in Taenia crassiceps by silencing Enolase A
    Julio Guerrero-Hernández, Raúl J. Bobes, Martín García-Varela, Alejandro Castellanos-Gonzalez, Juan P. Laclette
    Acta Tropica.2022; 225: 106197.     CrossRef
  • Taenia saginata Infection Misdiagnosed as Acute Cholecystitis in a Tibetan Patient, in China
    Xiu-Min Han, Xue-Yong Zhang, Ying-Na Jian, Qing-Shan Tian
    The Korean Journal of Parasitology.2021; 59(3): 311.     CrossRef
  • Current status of Opisthorchis viverrini, minute intestinal fluke and Taenia spp. infections among inhabitants in the Kenethao district of northern Lao PDR
    Phasouk Senephansiri, Thaksaporn Thongseesuksai, Phaviny Sithay, Sakhone Laymanivong, Thidarut Boonmar, Porntip Laummaunwai
    Transactions of The Royal Society of Tropical Medicine and Hygiene.2020; 114(5): 397.     CrossRef
  • Recent advances in nucleic acid-based methods for detection of helminth infections and the perspective of biosensors for future development
    Hanif Ullah, Abdul Qadeer, Muhammad Rashid, Muhammad Imran Rashid, Guofeng Cheng
    Parasitology.2020; 147(4): 383.     CrossRef
  • Mitochondrial Genome Sequences of <i>Spirometra erinaceieuropaei</i> and <i>S. decipiens</i> (Cestoidea: Diphyllobothriidae)
    Keeseon S. Eom, Hansol Park, Dongmin Lee, Seongjun Choe, Kyu-Heon Kim, Hyeong-Kyu Jeon
    The Korean Journal of Parasitology.2015; 53(4): 455.     CrossRef
  • Methods for Quantification of Soil-Transmitted Helminths in Environmental Media: Current Techniques and Recent Advances
    Philip A. Collender, Amy E. Kirby, David G. Addiss, Matthew C. Freeman, Justin V. Remais
    Trends in Parasitology.2015; 31(12): 625.     CrossRef
  • Rapid Molecular Identification of Human Taeniid Cestodes by Pyrosequencing Approach
    Tongjit Thanchomnang, Chairat Tantrawatpan, Pewpan M. Intapan, Oranuch Sanpool, Penchom Janwan, Viraphong Lulitanond, Somjintana Tourtip, Hiroshi Yamasaki, Wanchai Maleewong, Emmanuel Dias-Neto
    PLoS ONE.2014; 9(6): e100611.     CrossRef
  • Control of cysticercosis in Madagascar: beware of the pitfalls
    Harentsoaniaina Rasamoelina-Andriamanivo, Vincent Porphyre, Ronan Jambou
    Trends in Parasitology.2013; 29(11): 538.     CrossRef
  • 11,937 View
  • 119 Download
  • Crossref

Brief Communications

Production and Evaluation of Toxoplasma gondii Recombinant GRA7 for Serodiagnosis of Human Infections
Mina Selseleh, Hossein Keshavarz, Mehdi Mohebali, Saeedeh Shojaee, Monavar Selseleh, Mohammad Reza Eshragian, Fatemeh Mansouri, Mohammad Hossein Modarressi
Korean J Parasitol 2012;50(3):233-238.
Published online August 13, 2012
DOI: https://doi.org/10.3347/kjp.2012.50.3.233

The precise diagnosis of the acute toxoplasmosis in pregnant women and immunocompromsied patients has critical importance. Most of the commercially available assays use the whole Toxoplasma soluble extract as the antigen. However, the assays currently available for the detection of specific anti-Toxoplasma antibodies may vary in their abilities to detect serum immunoglobulins, due to the lack of a purified standardized antigen. The aim of this study was production and evaluation of the usefulness of the recombinant Toxoplasma gondii GRA7 antigen for the serodiagnosis of Toxoplasma gondii IgM and IgG by ELISA. A total of 70 T. gondii IgM positive sera, 74 T. gondii IgG positive sera, and 60 sera from subjects who were not infected with T. gondii were examined. These sera were shown different absorbance values in ELISA test. To control the specificity of the rGRA7 other parasitic diseases, for example, echinococcosis, malaria, leishmaniasis, fascioliasis, and strongyloidiasis were tested of which none showed positive results. Sensitivity and specificity of the generated recombinant IgG ELISA in comparison with commercial ELISA (com ELISA) were 89% and 90%, and the sensitivity and specificity of the generated recombinant IgM ELISA were 96% and 90%, respectively. The results obtained here show that this antigen is useful for diagnostic purposes.

Citations

Citations to this article as recorded by  Crossref logo
  • IgM Antibody Detection as a Diagnostic Marker for Acute Toxoplasmosis: Current Status of Studies and Main Limitations
    Karolina Sołowińska, Lucyna Holec-Gąsior
    Antibodies.2025; 14(2): 44.     CrossRef
  • Design of a Multi-epitope Antigen for Toxoplasmosis Diagnosis: An Immunoinformatics Approach
    Negar Asadi, Elham Yousefi, Sadegh Feizollahzadeh, Mortaza Taheri-Anganeh, Shahram Khademvatan, Gordon S. Howarth
    Acta Parasitologica.2025;[Epub]     CrossRef
  • The Spread of Toxoplasmosis in Women within Al-Rifai District
    Rehab Issa Hashem Suhail, Shimaa Ahmed Mutab Nayef, Teeba Sabah Daham Mohammed, Yaqeen Mohammed Mahmud, Abdalrhman Falah Omar Ali
    European Journal of Medical and Health Research.2024; 2(4): 257.     CrossRef
  • Trend in serological and molecular diagnostic methods for Toxoplasma gondii infection
    Min-ju Kim, Soeun J. Park, Hyunwoo Park
    European Journal of Medical Research.2024;[Epub]     CrossRef
  • Comparative Performance of Recombinant GRA6, GRA7, and GRA14 for the Serodetection of T. gondii Infection and Analysis of IgG Subclasses in Human Sera from the Philippines
    Rochelle Haidee Ybañez, Yoshifumi Nishikawa
    Pathogens.2022; 11(2): 277.     CrossRef
  • Utility of blood as the clinical specimen for the diagnosis of ocular toxoplasmosis using uracil DNA glycosylase-supplemented loop-mediated isothermal amplification and real-time polymerase chain reaction assays based on REP-529 sequence and B1 gene
    Bahman Rahimi Esboei, Shirzad Fallahi, Mohammad Zarei, Bahram Kazemi, Mehdi Mohebali, Saeedeh Shojaee, Parisa Mousavi, Aref Teimouri, Raziyeh Mahmoudzadeh, Mirataollah Salabati, Hossein Keshavarz Valian
    BMC Infectious Diseases.2022;[Epub]     CrossRef
  • Four Chemotherapeutic Compounds That Limit Blood-Brain-Barrier Invasion by Toxoplasma gondii
    Zijing Yan, Hao Yuan, Junjie Wang, Zipeng Yang, Pian Zhang, Yasser S. Mahmmod, Xiaohu Wang, Tanghui Liu, Yining Song, Zhaowen Ren, Xiu-Xiang Zhang, Zi-Guo Yuan
    Molecules.2022; 27(17): 5572.     CrossRef
  • Assessment of an In-House Enzyme-Linked Immunosorbent Assay and IgG Avidity Test Based on SAG1 and GRA7 Proteins for Discriminating between Acute and Chronic Toxoplasmosis in Humans
    Aref Teimouri, Mohammad Javad Abbaszadeh Afshar, Sina Mohtasebi, Sanaz Jafarpour Azami, Rasoul Alimi, Hossein Keshavarz, Bobbi S. Pritt
    Journal of Clinical Microbiology.2021;[Epub]     CrossRef
  • Enhancing Immune Responses to a DNA Vaccine Encoding Toxoplasma gondii GRA7 Using Calcium Phosphate Nanoparticles as an Adjuvant
    Hong-Chao Sun, Jing Huang, Yuan Fu, Li-Li Hao, Xin Liu, Tuan-Yuan Shi
    Frontiers in Cellular and Infection Microbiology.2021;[Epub]     CrossRef
  • Designing Diagnostic Kit for Toxoplasma gondii Based on GRA7, SAG1, and ROP1 Antigens: An In Silico Strategy
    Amirreza Javadi Mamaghani, Seyyed Javad Seyyed Tabaei, Mohammad Mehdi Ranjbar, Ali Haghighi, Adel Spotin, Parisa Ataee Dizaji, Hanieh Rezaee
    International Journal of Peptide Research and Therapeutics.2020; 26(4): 2269.     CrossRef
  • Serological detection of T. gondii infection in humans using an immunochromatographic assay based on dense granule protein 7
    Rochelle Haidee D. Ybañez, Yoshifumi Nishikawa
    Parasitology International.2020; 76: 102089.     CrossRef
  • Detection of antibodies against Toxoplasma gondii in cats using an immunochromatographic test based on GRA7 antigen
    Rochelle Haidee D. YBAÑEZ, Hisako KYAN, Yoshifumi NISHIKAWA
    Journal of Veterinary Medical Science.2020; 82(4): 441.     CrossRef
  • Review on the Current Trends of Toxoplasmosis Serodiagnosis in Humans
    Rochelle Haidee D. Ybañez, Adrian P. Ybañez, Yoshifumi Nishikawa
    Frontiers in Cellular and Infection Microbiology.2020;[Epub]     CrossRef
  • Identification of novel antigens for serum IgG diagnosis of human toxoplasmosis
    Juntao Luo, Jingyi Wan, Ziru Tang, Shuang Shen
    Experimental Parasitology.2019; 204: 107722.     CrossRef
  • Candidate antigenic epitopes for vaccination and diagnosis strategies of Toxoplasma gondii infection: A review
    Amirreza Javadi Mamaghani, Anwar Fathollahi, Adel Spotin, Mohammad mehdi Ranjbar, Meisam Barati, Somayeh Aghamolaie, Maryam Karimi, Niloofar Taghipour, Mohammad Ashrafi, Seyyed Javad Seyyed Tabaei
    Microbial Pathogenesis.2019; 137: 103788.     CrossRef
  • Advances in serological, imaging techniques and molecular diagnosis of Toxoplasma gondii infection
    Ali Rostami, Panagiotis Karanis, Shirzad Fallahi
    Infection.2018; 46(3): 303.     CrossRef
  • Antigens to Detect the Acute Phase of Toxoplasmosis in Pregnant Women: Standardized Comparison
    Juan Gabriel Costa, María Julia Vilariño
    Biomarkers in Medicine.2018; 12(5): 517.     CrossRef
  • Detection of toxoplasma-specific immunoglobulin G in human sera: performance comparison of in house Dot-ELISA with ECLIA and ELISA
    Aref Teimouri, Mohammad Hossein Modarressi, Saeedeh Shojaee, Mehdi Mohebali, Nima Zouei, Mostafa Rezaian, Hossein Keshavarz
    European Journal of Clinical Microbiology & Infectious Diseases.2018; 37(8): 1421.     CrossRef
  • The association of latent toxoplasmosis and level of serum testosterone in humans
    Nima Zouei, Saeedeh Shojaee, Mehdi Mohebali, Hossein Keshavarz
    BMC Research Notes.2018;[Epub]     CrossRef
  • The relation of secondary sex ratio and miscarriage history with Toxoplasma gondii infection
    Saeedeh Shojaee, Aref Teimouri, Hossein Keshavarz, Sanaz Jafarpour Azami, Sahar Nouri
    BMC Infectious Diseases.2018;[Epub]     CrossRef
  • Seroprevalence of Toxoplasma gondii and Neospora caninum infections in cattle in Mongolia
    Baldorj Pagmadulam, Punsantsogvoo Myagmarsuren, Ragab M. Fereig, Makoto Igarashi, Naoaki Yokoyama, Badgar Battsetseg, Yoshifumi Nishikawa
    Veterinary Parasitology: Regional Studies and Reports.2018; 14: 11.     CrossRef
  • Early detection of Toxoplasma gondii infection by using a interferon gamma release assay: A review
    Shima Mahmoudi, Setareh Mamishi, Xun Suo, Hossein Keshavarz
    Experimental Parasitology.2017; 172: 39.     CrossRef
  • Toxoplasma gondii GRA7-Targeted ASC and PLD1 Promote Antibacterial Host Defense via PKCα
    Hyun-Jung Koh, Ye-Ram Kim, Jae-Sung Kim, Jin-Seung Yun, Kiseok Jang, Chul-Su Yang, Sarah M. Fortune
    PLOS Pathogens.2017; 13(1): e1006126.     CrossRef
  • Dense Granule Protein-7 (GRA-7) of Toxoplasma gondii inhibits viral replication in vitro and in vivo
    Prasanna Weeratunga, Thilina U. B. Herath, Tae-Hwan Kim, Hyun-Cheol Lee, Jae-Hoon Kim, Byeong-Hoon Lee, Eun-Seo Lee, Kiramage Chathuranga, W. A. Gayan Chathuranga, Chul-Su Yang, Jin Yeul Ma, Jong-Soo Lee
    Journal of Microbiology.2017; 55(11): 909.     CrossRef
  • Cloning and Sequencing of Truncated Toxoplasma gondii Subtilisin-Like 1 Antigen
    Ahmad Rouhizadeh, Ata A Ghadiri, Mohammad Razi Jalali, Masoud Ghorbanpour, Mohammad Hossein Razi Jalali
    Zahedan Journal of Research in Medical Sciences.2016;[Epub]     CrossRef
  • Toxoplasma gondii GRA7-Induced TRAF6 Activation Contributes to Host Protective Immunity
    Chul-Su Yang, Jae-Min Yuk, Young-Ha Lee, Eun-Kyeong Jo, J. H. Adams
    Infection and Immunity.2016; 84(1): 339.     CrossRef
  • Production and Evaluation of Recombinant Granule Antigen Protein GRA7 for Serodiagnosis ofToxoplasma gondiiInfection in Cattle
    Zedong Wang, Wei Ge, Jiping Li, Mingxing Song, Hongchao Sun, Feng Wei, Quan Liu
    Foodborne Pathogens and Disease.2014; 11(9): 734.     CrossRef
  • Toxoplasma gondii infection: What is the real situation?
    Waenurama Chemoh, Nongyao Sawangjaroen, Veeranoot Nissapatorn, Chitkasaem Suwanrath, Verapol Chandeying, Thanaporn Hortiwakul, Hemah Andiappan, Natthawan Sermwittayawong, Bunsri Charoenmak, Pisut Siripaitoon, Amorn Lekkla, Yaowalark Sukthana
    Experimental Parasitology.2013; 135(4): 685.     CrossRef
  • Toxoplasma gondii Recombinant Antigens as Tools for Serodiagnosis of Human Toxoplasmosis: Current Status of Studies
    Lucyna Holec-Gąsior
    Clinical and Vaccine Immunology.2013; 20(9): 1343.     CrossRef
  • 9,116 View
  • 95 Download
  • Crossref
PCR Diagnosis of Entamoeba histolytica Cysts in Stool Samples
Joung-Ho Moon, Shin-Hyeong Cho, Jae-Ran Yu, Won-Ja Lee, Hyeng-Il Cheun
Korean J Parasitol 2011;49(3):281-284.
Published online September 30, 2011
DOI: https://doi.org/10.3347/kjp.2011.49.3.281

Amebiasis is a protozoan disease caused by Entamoeba histolytica and a potential health threat in areas where sanitation and hygiene are inappropriate. Highly sensitive PCR methods for detection of E. histolytica in clinical and environmental samples are extremely useful to control amebiasis and to promote public health. The present study compared several primer sets for small subunit (SSU) rDNA and histone genes of E. histolytica cysts. A 246 bp of the SSU rDNA gene of pure cysts contained in phosphate-buffered saline (PBS) and in stool samples was successfully amplified by nested PCR, using the 1,147-246 bp primer set, of the primary PCR products which were pre-amplified using the 1,147 bp primer as the template. The detection limit of the nested PCR using the 1,147-246 primer set was 10 cysts in both groups (PBS and stool samples). The PCR to detect histone gene showed negative results. We propose that the nested PCR technique to detect SSU rDNA can be used as a highly sensitive genetic method to detect E. histolytica cysts in stool samples.

Citations

Citations to this article as recorded by  Crossref logo
  • Practical Guidance for Clinical Microbiology Laboratories: Laboratory Diagnosis of Parasites from the Gastrointestinal Tract
    Lynne S. Garcia, Michael Arrowood, Evelyne Kokoskin, Graeme P. Paltridge, Dylan R. Pillai, Gary W. Procop, Norbert Ryan, Robyn Y. Shimizu, Govinda Visvesvara
    Clinical Microbiology Reviews.2018;[Epub]     CrossRef
  • Evaluation of recombinant multi-epitope proteins for diagnosis of goat schistosomiasis by enzyme-linked immunosorbent assay
    Chao Lv, Yang Hong, Zhiqiang Fu, Ke Lu, Xiaodan Cao, Tao Wang, Chuangang Zhu, Hao Li, Rui Xu, Bingguang Jia, Qian Han, Xuefeng Dou, Yuanxi Shen, Zuhang Zhang, Jinli Zai, Jintao Feng, Jiaojiao Lin
    Parasites & Vectors.2016;[Epub]     CrossRef
  • Frequency of amoebiasis and other intestinal parasitoses in a settlement in Ilhéus City, State of Bahia, Brazil
    Helena Lúcia Carneiro Santos, Luci Ana Fernandes Martins, Regina Helena Saramago Peralta, José Mauro Peralta, Heloisa Werneck de Macedo
    Revista da Sociedade Brasileira de Medicina Tropical.2014; 47(1): 101.     CrossRef
  • 9,659 View
  • 101 Download
  • Crossref

Original Articles

Development and Clinical Evaluation of a Rapid Serodiagnostic Test for Toxoplasmosis of Cats Using Recombinant SAG1 Antigen
Chom-Kyu Chong, Wooseog Jeong, Hak-Yong Kim, Dong-Jun An, Hye-Young Jeoung, Jeong-Eun Ryu, A-Ra Ko, Yong-Joo Kim, Sung-Jong Hong, Zhaoshou Yang, Ho-Woo Nam
Korean J Parasitol 2011;49(3):207-212.
Published online September 30, 2011
DOI: https://doi.org/10.3347/kjp.2011.49.3.207

Rapid serodiagnostic methods for Toxoplasma gondii infection in cats are urgently needed for effective control of transmission routes toward human infections. In this work, 4 recombinant T. gondii antigens (SAG1, SAG2, GRA3, and GRA6) were produced and tested for the development of rapid diagnostic test (RDT). The proteins were expressed in Escherichia coli, affinity-purified, and applied onto the nitrocellulose membrane of the test strip. The recombinant SAG1 (rSAG1) showed the strongest antigenic activity and highest specificity among them. We also performed clinical evaluation of the rSAG1-loaded RDT in 182 cat sera (55 household and 127 stray cats). The kit showed 0.88 of kappa value comparing with a commercialized ELISA kit, which indicated a significant correlation between rSAG1-loaded RDT and the ELISA kit. The overall sensitivity and specificity of the RDT were 100% (23/23) and 99.4% (158/159), respectively. The rSAG1-loaded RDT is rapid, easy to use, and highly accurate. Thus, it would be a suitable diagnostic tool for rapid detection of antibodies in T. gondii-infected cats under field conditions.

Citations

Citations to this article as recorded by  Crossref logo
  • Development and optimization of an ELISA method to detect Toxoplasma gondii oocyst infection in cats
    Mingfeng He, Bufan Zhang, Shuai Han, Jiahui Qian, Zhengming He, Yulian Wei, Yanqin Zhou, Bang Shen, Rui Fang
    Parasitology Research.2025;[Epub]     CrossRef
  • Comprehensive diagnostic approaches to feline toxoplasmosis: Bridging traditional methods and emerging technologies
    Dan Zhao, Yanzhen Liao, Hao Liu, Jianwei Wang, Ruiying Liang, Rongqiong Zhou, Jiabo Ding, Sixin Zhang, Xinming Tang
    Virulence.2025;[Epub]     CrossRef
  • Evaluation of an immunochromatographic serologic test to detect the presence of anti‐Toxoplasma gondii antibodies in cats
    Sergio Villanueva‐Saz, Mariví Martínez, Jacobo Giner, María Dolores Pérez, Ana Pilar Tobajas, Andrés Yzuel, María Teresa Verde, Delia Lacasta, Antonio Fernández, Diana Marteles, Héctor Ruíz
    Veterinary Clinical Pathology.2023; 52(2): 284.     CrossRef
  • A preliminary study to develop a lateral flow assay using recombinant GRA1 protein for the diagnosis of toxoplasmosis in stray cats
    Aysu Değirmenci Döşkaya, Hüseyin Can, Aytül Gül, Tuğba Karakavuk, Mervenur Güvendi, Muhammet Karakavuk, Ceren Gül, Sedef Erkunt Alak, Cemal Ün, Adnan Yüksel Gürüz, Mert Döşkaya
    Comparative Immunology, Microbiology and Infectious Diseases.2023; 101: 102057.     CrossRef
  • Development and evaluation of indirect enzyme-linked immunosorbent assay using recombinant dense granule antigen 7 protein for the detection of Toxoplasma gondii infection in cats in Thailand
    Eukote Suwan, Piangjai Chalermwong, Rucksak Rucksaken, Metita Sussadee, Sarawan Kaewmongkol, Ruenruetai Udonsom, Sathaporn Jittapalapong, Bandid Mangkit
    Veterinary World.2022; : 602.     CrossRef
  • Serological and molecular rapid diagnostic tests for Toxoplasma infection in humans and animals
    Amjad Hayat Khan, Rahmah Noordin
    European Journal of Clinical Microbiology & Infectious Diseases.2020; 39(1): 19.     CrossRef
  • All about toxoplasmosis in cats: the last decade
    J.P. Dubey, C.K. Cerqueira-Cézar, F.H.A. Murata, O.C.H. Kwok, Y.R. Yang, C. Su
    Veterinary Parasitology.2020; 283: 109145.     CrossRef
  • Toxoplasma gondii Recombinant Antigens in the Serodiagnosis of Toxoplasmosis in Domestic and Farm Animals
    Bartłomiej Ferra, Lucyna Holec-Gąsior, Weronika Grąźlewska
    Animals.2020; 10(8): 1245.     CrossRef
  • Fluorescent bead-based serological detection of Toxoplasma gondii infection in chickens
    Benedikt T. Fabian, Fatima Hedar, Martin Koethe, Berit Bangoura, Pavlo Maksimov, Franz J. Conraths, Isabelle Villena, Dominique Aubert, Frank Seeber, Gereon Schares
    Parasites & Vectors.2020;[Epub]     CrossRef
  • Development and Clinical Evaluation of a Rapid Diagnostic Test for Yellow Fever Non-Structural Protein 1
    Yeong Hoon Kim, Tae-Yun Kim, Ji-Seon Park, Jin Suk Park, Jihoo Lee, Joungdae Moon, Chom-Kyu Chong, Ivan Neves Junior, Fernando Raphael Ferry, Hye-Jin Ahn, Lokraj Bhatt, Ho-Woo Nam
    The Korean Journal of Parasitology.2019; 57(3): 283.     CrossRef
  • Development of a Rapid Diagnostic Test Kit to Detect IgG/IgM Antibody against Zika Virus Using Monoclonal Antibodies to the Envelope and Non-structural Protein 1 of the Virus
    Yeong Hoon Kim, Jihoo Lee, Young-Eun Kim, Chom-Kyu Chong, Yanaihara Pinchemel, Francis Reisdörfer, Joyce Brito Coelho, Ronaldo Ferreira Dias, Pan Kee Bae, Zuinara Pereira Maia Gusmão, Hye-Jin Ahn, Ho-Woo Nam
    The Korean Journal of Parasitology.2018; 56(1): 61.     CrossRef
  • Disentangling the link between supplemental feeding, population density, and the prevalence of pathogens in urban stray cats
    Jusun Hwang, Nicole L. Gottdenker, Dae-Hyun Oh, Ho-Woo Nam, Hang Lee, Myung-Sun Chun
    PeerJ.2018; 6: e4988.     CrossRef
  • Spread and genotype of Toxoplasma gondii in naturally infected alpine chamois (Rupicapra r. rupicapra)
    Nicoletta Formenti, Alessandra Gaffuri, Tiziana Trogu, Roberto Viganò, Nicola Ferrari, Paolo Lanfranchi
    Parasitology Research.2016; 115(5): 2115.     CrossRef
  • Opportunities and challenges for the application of microfluidic technologies in point-of-care veterinary diagnostics
    Valentina Busin, Beth Wells, Maïwenn Kersaudy-Kerhoas, Wenmaio Shu, Stewart T.G. Burgess
    Molecular and Cellular Probes.2016; 30(5): 331.     CrossRef
  • Synthesis and characterization of latex-protein complexes from different antigens ofToxoplasma gondiifor immunoagglutination assays
    Leandro E. Peretti, Verónica D. G. Gonzalez, Juan G. Costa, Iván S. Marcipar, Luis M. Gugliotta
    International Journal of Polymeric Materials and Polymeric Biomaterials.2016; 65(18): 938.     CrossRef
  • Toxoplasma gondii Infection in Alpine Red Deer (Cervus elaphus): Its Spread and Effects on Fertility
    Nicoletta Formenti, Tiziana Trogu, Luca Pedrotti, Alessandra Gaffuri, Paolo Lanfranchi, Nicola Ferrari, Guido Favia
    PLOS ONE.2015; 10(9): e0138472.     CrossRef
  • Latex–protein complexes from an acute phase recombinant antigen of Toxoplasma gondii for the diagnosis of recently acquired toxoplasmosis
    Leandro E. Peretti, Verónica D.G. Gonzalez, Iván S. Marcipar, Luis M. Gugliotta
    Colloids and Surfaces B: Biointerfaces.2014; 120: 88.     CrossRef
  • A Rapid Diagnostic Test for Toxoplasmosis using Recombinant Antigenic N-terminal Half of SAG1 Linked with Intrinsically Unstructured Domain of GRA2 Protein
    Kyoung Ju Song, Zhaoshou Yang, Chom-Kyu Chong, Jin-Soo Kim, Kyung Chan Lee, Tong-Soo Kim, Ho-Woo Nam
    The Korean Journal of Parasitology.2013; 51(5): 503.     CrossRef
  • Evaluation of an indirect ELISA using a tachyzoite surface antigen SAG1 for diagnosis of Toxoplasma gondii infection in cats
    M. Hosseininejad
    Experimental Parasitology.2012; 132(4): 556.     CrossRef
  • 10,550 View
  • 121 Download
  • Crossref
Evaluation of Rapid Diagnostics for Plasmodium falciparum and P. vivax in Mae Sot Malaria Endemic Area, Thailand
Wanna Chaijaroenkul, Thanee Wongchai, Ronnatrai Ruangweerayut, Kesara Na-Bangchang
Korean J Parasitol 2011;49(1):33-38.
Published online March 18, 2011
DOI: https://doi.org/10.3347/kjp.2011.49.1.33

Prompt and accurate diagnosis of malaria is the key to prevent disease morbidity and mortality. This study was carried out to evaluate diagnostic performance of 3 commercial rapid detection tests (RDTs), i.e., Malaria Antigen Pf/Pan™, Malaria Ag-Pf™, and Malaria Ag-Pv™ tests, in comparison with the microscopic and PCR methods. A total of 460 blood samples microscopically positive for Plasmodium falciparum (211 samples), P. vivax (218), mixed with P. falciparum and P. vivax (30), or P. ovale (1), and 124 samples of healthy subjects or patients with other fever-related infections, were collected. The sensitivities of Malaria Ag-Pf™ and Malaria Antigen Pf/Pan™ compared with the microscopic method for P. falciparum or P. vivax detection were 97.6% and 99.0%, or 98.6% and 99.0%, respectively. The specificities of Malaria Ag-Pf™, Malaria Ag-Pv™, and Malaria Antigen Pf/Pan™ were 93.3%, 98.8%, and 94.4%, respectively. The sensitivities of Malaria Ag-Pf™, Malaria Antigen Pf/Pan™, and microscopic method, when PCR was used as a reference method for P. falciparum or P. vivax detection were 91.8%, 100%, and 96.7%, or 91.9%, 92.6%, and 97.3%, respectively. The specificities of Malaria Ag-Pf™, Malaria Ag-Pv™, Malaria Antigen Pf/Pan™, and microscopic method were 66.2%, 92.7%, 73.9%, and 78.2%, respectively. Results indicated that the diagnostic performances of all the commercial RDTs are satisfactory for application to malaria diagnosis.

Citations

Citations to this article as recorded by  Crossref logo
  • Multiplexed quantitative proteomics provides mechanistic cues for malaria severity and complexity
    Vipin Kumar, Sandipan Ray, Shalini Aggarwal, Deeptarup Biswas, Manali Jadhav, Radha Yadav, Sanjeev V. Sabnis, Soumaditya Banerjee, Arunansu Talukdar, Sanjay K. Kochar, Suvin Shetty, Kunal Sehgal, Swati Patankar, Sanjeeva Srivastava
    Communications Biology.2020;[Epub]     CrossRef
  • DIAGNOSTIC PERFORMANCE EVALUATION OF THE SD BIOLINE MALARIA ANTIGEN AG PF/PAN TEST (05FK60) IN A MALARIA ENDEMIC AREA OF SOUTHERN ETHIOPIA
    Endale TADESSE, Bereket WORKALEMAHU, Techalew SHIMELIS
    Revista do Instituto de Medicina Tropical de São Paulo.2016;[Epub]     CrossRef
  • Epidemiological aspects of vivax and falciparum malaria: global spectrum
    Shyamapada Mandal
    Asian Pacific Journal of Tropical Disease.2014; 4: S13.     CrossRef
  • Nested-PCR and a New ELISA-Based NovaLisa Test Kit for Malaria Diagnosis in an Endemic Area of Thailand
    Pimwan Thongdee, Wanna Chaijaroenkul, Jiraporn Kuesap, Kesara Na-Bangchang
    The Korean Journal of Parasitology.2014; 52(4): 377.     CrossRef
  • Rapid diagnostic tests for diagnosing uncomplicated non-falciparum or Plasmodium vivax malaria in endemic countries
    Katharine Abba, Amanda J Kirkham, Piero L Olliaro, Jonathan J Deeks, Sarah Donegan, Paul Garner, Yemisi Takwoingi
    Cochrane Database of Systematic Reviews.2014;[Epub]     CrossRef
  • 9,667 View
  • 83 Download
  • Crossref

Brief Communications

Evaluation of Two ELISA and Two Indirect Hemagglutination Tests for Serodiagnosis of Pulmonary Hydatid Disease
Fatma Nur Eris, Ciler Akisu, Umit Aksoy
Korean J Parasitol 2009;47(4):427-429.
Published online December 1, 2009
DOI: https://doi.org/10.3347/kjp.2009.47.4.427

To establish a definite diagnosis for pulmonary hydatid disease, combination of radiology and serology is useful. In this study, 19 preoperative sera from patients with surgically confirmed pulmonary hydatidosis, 40 sera from patients with other parasitosis and pulmonary diseases, and 20 sera from healthy donors were evaluated using 4 different serological tests, i.e., the commercial ELISA (ELISA-kit) test, the ELISA (ELISA-lab) test prepared in our laboratory, the commercial indirect hemagglutination assay kit (IHA-kit) test, and the IHA test using sensitized sheep red blood cells with tannic acid (IHA-TA). The ELISA-kit was the most sensitive (84.2%) and the most specific test (100.0%). The ELISA-kit also demonstrated the highest positive (100.0%) and negative (95.2%) predictive values. The sensitivity of the ELISA-lab test, that we prepared, was found to be 73.6%, whereas the IHA-kit test and the IHA-TA test were found to be 73.6% and 68.4%, respectively. The specificity of these tests was 96.6%, 98.3%, and 83.3%, respectively. When all 4 tests were assessed together, it was found that the sensitivity had risen to 94.7%. When the ELISA-kit was assessed with the IHA-kit and IHA-TA together, it was found that the sensitivity was 89.5% and 84.2%, respectively. Likewise, the combination of the ELISA-lab and IHA-kit or IHA-TA allowed us to achieve a sensitivity of 84.2% in cases of pulmonary echinococcosis. In conclusion, the diagnosis would be imminent if least 2 tests were applied together.

Citations

Citations to this article as recorded by  Crossref logo
  • The role of ELISA IgG antibodies in diagnosis of cystic echinococosis of lung. A retrospective study of a single centre activity in Albania
    Fatmir Caushi, Eritjan Tashi, Arben Tanka, Arian Mezini, Valbona Gjoni, Ilir Skenduli, Silva Tafaj, Silvana Bala, Ornela Nuredini, Agron Meshi, Emira Hysa, Francesco Rulli
    Journal of Cardiothoracic Surgery.2025;[Epub]     CrossRef
  • Design and evaluation of a novel direct hemagglutination test based on a recombinant protein for diagnosis of cystic echinococcosis
    Abolfazl Masoumi Koushk Mehdi, Hossein Motedayyen, Majid Fasihi Harandi, Hossein Akbari, Amin Moradi Hasan-Abad, Mohsen Arbabi
    Parasites & Vectors.2025;[Epub]     CrossRef
  • EgSeverin and Eg14-3-3zeta from Echinococcus granulosus are potential antigens for serological diagnosis of echinococcosis in dogs and sheep
    Xiaoli Zhang, Chenxi Wei, Yajie Lv, Rongsheng Mi, Baoping Guo, Sajid Ur Rahman, Yehua Zhang, Long Cheng, Haiyan Jia, Yan Huang, Xiangan Han, Haiyan Gong, Zhaoguo Chen
    Microbial Pathogenesis.2023; 179: 106110.     CrossRef
  • Human cystic echinococcosis: Serological diagnosis by indirect hemagglutination test, enzyme-linked immunosorbent assay, immunoelectrophoresis, and immunoblotting in surgically confirmed patients versus cases diagnosed by imaging techniques
    H. Zait, B. Hamrioui
    Médecine et Maladies Infectieuses.2020; 50(8): 676.     CrossRef
  • Cystic echinococcosis in Jordan: A review of causative species, previous studies, serological and radiological diagnosis
    Nawal S. Hijjawi, Ali M. Al-Radaideh, Eman M. Rababah, Khaled M. Al-Qaoud, Kamal E. Bani-Hani
    Acta Tropica.2018; 179: 10.     CrossRef
  • Serological Evidence of Echinococcosis in Municipality Workers in United Arab Emirates
    Doaa Moustafa Sultan, Seyed Mahmoud Sadjjadi, Naglaa Raafat AbdRaboh
    Research Journal of Parasitology.2016; 11(3): 33.     CrossRef
  • Norway rat (Rattus norvegicus) as a potential reservoir for Echinococcus granulosus: A public health implication
    Khaled A. Abdel-Moein, Dalia A. Hamza
    Acta Parasitologica.2016;[Epub]     CrossRef
  • Mediastinal mass and hydatid disease
    M. S. Thakkar, C. F. N. Koegelenberg, J. Bezuidenhout, E. M. Irusen
    QJM.2013; 106(12): 1127.     CrossRef
  • Extrahepatic Primary Adrenal Alveolar Echinococcosis: A Review
    Zhi-gang Chu, Fa-jin Lv, Zhi-yu Zhu, Yu Ouyang
    Surgical Infections.2013; 14(4): 418.     CrossRef
  • Serodiagnosis of human hydatidosis with an ELISA developed based on antigens derived from sheep hydatid cysts and comparison with a commercial human ELISA kit
    S Fotoohi, G.R Hashemi Tabar, H Borji
    Asian Pacific Journal of Tropical Medicine.2013; 6(9): 723.     CrossRef
  • Cross-Reaction between the Crude Hydatid Cyst Fluid Antigens of Human and Animals Origin in Response to Human IgG Class and Subclasses
    Afra Khosravi, Sobhan Ghafourian, Morteza Shamsi, Nourkhoda Sadeghifard, Abbas Maleki, Ebrahim Babaahmadi
    Journal of Parasitology Research.2012; 2012: 1.     CrossRef
  • 15,537 View
  • 80 Download
  • Crossref
Prevalence of Malaria in Pregnant Women in Lagos, South-West Nigeria
Chimere O. Agomo, Wellington A. Oyibo, Rose I. Anorlu, Philip U. Agomo
Korean J Parasitol 2009;47(2):179-183.
Published online May 27, 2009
DOI: https://doi.org/10.3347/kjp.2009.47.2.179

Prevalence rates reported for malaria in pregnancy in Nigeria vary considerably. The accuracy of results of malaria diagnosis is dependent on training, experience, and motivation of the microscopist as well as the laboratory facility available. Results of training programmes on malaria microscopy have shown low levels of sensitivity and specificity of those involved in malaria diagnosis routinely and for research. This study was done to ascertain the true prevalence of malaria in pregnancy in Lagos, South-West Nigeria. A total of 1,084 pregnant women were recruited into this study. Blood smears stained with Giemsa were used for malaria diagnosis by light microscopy. Malaria infection during pregnancy presents mostly as asymptomatic infection. The prevalence of malaria in this population was 7.7% (95% confidence interval; 6.2-9.4%). Factors identified to increase the risk of malaria infection include young maternal age (< 20 years), and gravidity (primigravida). In conclusion, this study exposes the over-diagnosis of malaria in pregnancy and the need for training and retraining of laboratory staffs as well as establishing the malaria diagnosis quality assurance programme to ensure the accuracy of malaria microscopy results at all levels.

Citations

Citations to this article as recorded by  Crossref logo
  • Prevalence, characteristics, and treatment outcome of congenital malaria in Nigeria: a systematic review
    Emmanuel Kokori, Gbolahan Olatunji, Bonaventure Michael Ukoaka, Israel Charles Abraham, Rosemary Komolafe, Victor Oluwatomiwa Ajekiigbe, Ntishor Gabriel Udam, Stanley Eneh, Chidiogo Ezenwoba, Adetola Emmanuel Babalola, Oluwatobi Omoworare, Nicholas Aderin
    Malaria Journal.2025;[Epub]     CrossRef
  • Congenital infection with Plasmodium malariae: a rare case of intrauterine transmission in Germany
    Sarah Goretzki, Nora Bruns, Anna Daniels, Anne Schönecker, Adela Della Marina, Andrea Gangfuß, Bernd Schweiger, Andreas Schönfeld, Oliver Witzke, Jutta Dedy, Jan Dziobaka, Caroline Holtkamp, Peter-Michael Rath, Ursula Felderhoff-Müser, Christian Dohna-Sch
    Malaria Journal.2025;[Epub]     CrossRef
  • Spatial variation and multilevel determinants of malaria infection among pregnant women in Sub-Saharan Africa: using malaria indicator surveys
    Alebachew Ferede Zegeye, Enyew Getaneh Mekonen, Deresse Abebe Gebrehana, Berhan Tekeba, Tadesse Tarik Tamir
    BMC Infectious Diseases.2025;[Epub]     CrossRef
  • Assessing predictors and outcomes of suspected fetal compromise during labor in a Nigerian tertiary hospital: a retrospective cohort analysis
    Ayokunle Moses Olumodeji, Taiwo Kuku-Kuye, Oluwabunmi Christiana Oyebode, Ayodeji Kayode Adefemi, Modupe Olatokunbo Adedeji, Yusuf Abisowo Oshodi, Kabiru Afolarin Rabiu, Oluwarotimi Ireti Akinola
    Discover Medicine.2025;[Epub]     CrossRef
  • Intermittent preventive treatment, malaria, HIV, hepatitis and pregnancy outcomes in Nigerian women: a cross-sectional study in two healthcare facilities
    Rebecca Chinyelu Chukwuanukwu, George Uchenna Eleje, Felix Emeka Menkiti, Golibe Christian Ikpeze, Chioma Ngozichukwu Mbachu, Nnaedozie Paul Obiegbu, Confidence Chinaza Ogbomade, Hatesin Ifeanyi Anyaegbu, Alfred Friday Ehiaghe, Dorothy Amauche Ezeagwuna,
    BMC Pregnancy and Childbirth.2025;[Epub]     CrossRef
  • Malaria-anemia comorbidity and its determinants among pregnant women in high- and moderate-malaria-risk countries in Sub-Saharan Africa
    Alebachew Ferede Zegeye, Mulugeta Wassie, Tadesse Tarik Tamir, Berhan Tekeba, Enyew Getaneh Mekonen, Gebreeyesus Abera Zeleke, Deresse Abebe Gebrehana
    Infectious Diseases of Poverty.2025;[Epub]     CrossRef
  • Malaria in Pregnancy and Predisposing Factors in Jor District of Gambella Region, Southwest Ethiopia: A Cross‐Sectional Study
    Okwom Oguta, Jemal Mohammed, Ukash Umer, Ephrem Tefera Solomon
    Health Science Reports.2025;[Epub]     CrossRef
  • Prevalence, and Biosocial Associations, of Malaria Parasitemia in Pregnant Women from Southeastern Nigeria
    Stella Ekene Ogamba, Joseph Ifeanyi Brian-D Adinma, Nneoma Dolores Adinma-Obiajulu, Edith Nonye Nwankwo, Mark Matthew Edet, Nneoma Victoria Okpala, Dennis N. Aribodor
    Journal of the Nigerian Academy of Medicine.2024; 3(1): 8.     CrossRef
  • Trends in malaria prevention and vector control intervention among pregnant women and children under 5 years in Nigeria
    Felix Olaniyi Sanni, Ahmed Mamuda Bello, Oyewande Azeezat Abimbola, Ishata Nannie Conteh, Adebanke Adetutu Ogun, Abimbola Oluseyi Ariyo, Olaide Lateef Afelumo, Michael Olabode Tomori, Olubunmi Elizabeth Amoo, Anthony Chuks Aguh, Abiodun Olakunle Ogunniyi,
    MGM Journal of Medical Sciences.2023; 10(2): 287.     CrossRef
  • Malaria and HIV Co-Infection among Pregnant Women in Africa: Prevalence, Effect on Immunity and Clinical Management: Review
    Bekindaka Ngemani Obase, Jude Daiga Bigoga, Dickson Shey Nsagha
    International Journal of Translational Medicine.2023; 3(2): 187.     CrossRef
  • AEMATOLOGICAL CHANGES IN MALARIA INFECTION AMONG PREGNANT WOMEN IN SOKOTO METROPOLIS NIGERIA
    I. Garba, A. I. Umar, M. B. Tijjani, M. S. Aliyu, H. I. D. Muhammad, M. I. O. Raji, S. A. Fana, J. Thompson
    FUDMA JOURNAL OF SCIENCES.2023; 7(3): 283.     CrossRef
  • Prevalence and Risk Factors Associated with Malaria among Pregnant Women Attending Selected Public Health Facilities within Katsina Metropolis, Katsina State, Nigeria
    Saratu Lawal, Abdulhamid Ahmed, Umar Lawal
    UMYU Journal of Microbiology Research (UJMR).2023; 8(2): 8.     CrossRef
  • Malaria in pregnancy
    Edith C Ikpeama, Peter C Udealor, Chidinma I Onwuka
    International Journal of Medicine and Health Development.2022; 27(4): 356.     CrossRef
  • Prevalence of pregnancy complications in Nnewi, South-East Nigeria
    Anulika J. Afonne, Jerome O. Okafor
    Egyptian Nursing Journal.2022; 19(1): 1.     CrossRef
  • Pregnancy experiences and maternal health service utilisation among female traders in Ibadan, Nigeria
    Oludoyinmola O. Ojifinni, Oluwafemi A. Popoola
    Journal of Public Health.2021; 29(2): 293.     CrossRef
  • Asymptomatic malaria infection prevailing risks for human health and malaria elimination
    Dhaneswar Prusty, Nidhi Gupta, Arun Upadhyay, Ashraf Dar, Biswajit Naik, Navin Kumar, Vijay Kumar Prajapati
    Infection, Genetics and Evolution.2021; 93: 104987.     CrossRef
  • Hepatitis B and Asymptomatic Malaria Infection among Pregnant Women in a Semiurban Community of North-Central Nigeria
    Cornelius Arome Omatola, Martin-Luther Oseni Okolo, John Yabe
    Journal of Environmental and Public Health.2021; 2021: 1.     CrossRef
  • Vitex negundo L. Essential Oil: Odorant Binding Protein Efficiency Using Molecular Docking Approach and Studies of the Mosquito Repellent
    Bamidele Joseph Okoli, Zakari Ladan, Fanyana Mtunzi, Yayock Chigari Hosea
    Insects.2021; 12(12): 1061.     CrossRef
  • Effects of malaria parasitaemia on foetal middle cerebral artery doppler indices in a cohort of pregnant Nigerian women
    CM Asaleye, EO Isaac-Okolo, AS Aderibigbe, OM Loto, AK Abidoye, OO Ayoola
    Nigerian Journal of Health Sciences.2021; 21(2): 43.     CrossRef
  • “Dual-gene” malaria-resistance: Therapeutically-rational exchange (T-REX) of group-O sickle trait and group-O C-traittrait red blood cells can be evaluated in Benin and Nigeria
    Ryan Philip Jajosky, Audrey N. Jajosky, Philip G. Jajosky
    Transfusion and Apheresis Science.2020; 59(3): 102733.     CrossRef
  • Effect of Impregnated Mosquito Bed Nets on the Prevalence of Malaria among Pregnant Women in Foumban Subdivision, West Region of Cameroon
    Ngouyamsa N. A. Sidiki, Vincent Khan Payne, Yamssi Cedric, Noumedem A. C. Nadia
    Journal of Parasitology Research.2020; 2020: 1.     CrossRef
  • Prevalence and associated factors of malaria among pregnant women in Sherkole district, Benishangul Gumuz regional state, West Ethiopia
    Girma Bekele Gontie, Haileab Fekadu Wolde, Adhanom Gebreegziabher Baraki
    BMC Infectious Diseases.2020;[Epub]     CrossRef
  • Determinants of uptake of first dose of intermittent preventive treatment among pregnant women in a secondary health Centre in Maiduguri, Nigeria
    Ahmed Dahiru Balami, Salmiah Md. Said, Nor Afiah Mohd. Zulkefli, Norsa’adah Bachok, Bala Audu
    BMC Pregnancy and Childbirth.2020;[Epub]     CrossRef
  • Anemia in Pregnancy: Urban–Rural Comparison of Management and Prevention Among Women of Child-Bearing Age in Anambra State, Nigeria
    Obianuju U. Igweonu, Nkechi G. Onyeneho
    International Quarterly of Community Health Education.2019; 39(3): 155.     CrossRef
  • A randomized controlled trial of azithromycin and sulphadoxine–pyrimethamine as prophylaxis against malaria in pregnancy among human immunodeficiency virus–positive women
    Oriyomi Akinyotu, Folasade Bello, Rukiyat Abdus-Salam, Ayodele Arowojolu
    Transactions of The Royal Society of Tropical Medicine and Hygiene.2019; 113(8): 463.     CrossRef
  • Malaria Prevention Measures among Pregnant Women: A Population-Based Survey in Nnewi, Nigeria
    Devender Bhalla, Laurent Cleenewerck, Stephen Okorafor Kalu, Kabiru Abubakar Gulma
    The Scientific World Journal.2019; 2019: 1.     CrossRef
  • Risk factors associated with malaria infection among pregnant women of African Descent in Specialist Hospital Sokoto, Nigeria
    Osaro Erhabo, Abdulrahaman Abdullahi, Erhabor Tosan, Adias Teddy Charles
    Obstetrics & Gynecology International Journal.2019;[Epub]     CrossRef
  • High prevalence of dihydrofolate reductase gene mutations inPlasmodium falciparumparasites among pregnant women in Nigeria after reported use of sulfadoxine-pyrimethamine
    Olusola Ojurongbe, Christian N. Nguetse, Samuel A. Fayemiwo, Catherine O. Falade, Taiwo A. Ojurongbe, Bolaji N. Thomas, Christian G. Meyer, Thirumalaisamy P. Velavan
    Pathogens and Global Health.2018; 112(2): 86.     CrossRef
  • Malaria in pregnancy: Two-year prevalence among women attending antenatal clinics in a Nigerian hospital
    Andy Emmanuel, Grace Onyejekwe, Esther Funke Adeleke
    African Journal of Midwifery and Women's Health.2018; 12(3): 117.     CrossRef
  • Evaluation of Renal Function in Pregnant Women with Malaria: A Case-Control Study in a Mesoendemic Area
    Justice Afrifa, Samuel Essien-Baidoo, Albert Baffour Gyau, Richard Kobina Dadzie Ephraim
    Obstetrics and Gynecology International.2017; 2017: 1.     CrossRef
  • Antenatal Practices Ineffective at Prevention of Plasmodium falciparum Malaria during Pregnancy in a Sub-Saharan Africa Region, Nigeria
    Ifeanyi Oscar Ndimkaoha Aguzie, Njoku Ivoke, Grace C. Onyishi, Ikem C. Okoye
    Tropical Medicine and Infectious Disease.2017; 2(2): 15.     CrossRef
  • Rapid Diagnostic Test Kits Detection of Malaria Parasites among Pregnant Women Attending Antenatal in Selected Hospitals in Anyigba, Kogi State, Nigeria
    Clement Ameh Yaro, Florence Oyibo Iyaji, Michael Obanogbon Tope
    Advances in Bioscience and Biotechnology.2017; 08(08): 249.     CrossRef
  • Determinants of Malaria Prevention and Treatment Seeking Behaviours of Pregnant Undergraduates Resident in University Hostels, South-East Nigeria
    Anthonia Ukamaka Chinweuba, Noreen Ebelechukwu Agbapuonwu, JaneLovena Enuma Onyiapat, Chidimma Egbichi Israel, Clementine Ifeyinwa Ilo, Joyce Chinenye Arinze
    Journal of Pregnancy.2017; 2017: 1.     CrossRef
  • Malaria prevalence, severity and treatment outcome in relation to day 7 lumefantrine plasma concentration in pregnant women
    Ritah F. Mutagonda, Appolinary A. R. Kamuhabwa, Omary M. S. Minzi, Siriel N. Massawe, Betty A. Maganda, Eleni Aklillu
    Malaria Journal.2016;[Epub]     CrossRef
  • Prevalence of malaria and associated factors in Benna Tsemay district of pastoralist community, Southern Ethiopia
    Gidie Woju Debo, Dejene Hailu Kassa
    Tropical Diseases, Travel Medicine and Vaccines.2016;[Epub]     CrossRef
  • Assessment of Markers of Antimalarial Drug Resistance in Plasmodium falciparum Isolates from Pregnant Women in Lagos, Nigeria
    Chimere Obiora Agomo, Wellington Aghoghovwia Oyibo, Colin Sutherland, Rachael Hallet, Mary Oguike, Thomas A. Smith
    PLOS ONE.2016; 11(1): e0146908.     CrossRef
  • Prevalence of Malaria Parasitaemia among Pregnant Women Attending Three Selected Health Centers in Ideato South Local Government Area, Imo State
    Frank Maureen D
    Obstetrics & Gynecology International Journal.2016;[Epub]     CrossRef
  • Prevalence and risk factors associated with malaria infection among pregnant women in a semi-urban community of north-western Nigeria
    Sani Abdullahi Fana, Mohammed Danladi Abubakar Bunza, Sule Aliyu Anka, Asiya Umar Imam, Shehu Usman Nataala
    Infectious Diseases of Poverty.2015;[Epub]     CrossRef
  • Schistosoma haematobium and Plasmodium falciparum single and concomitant infections; any association with hematologic abnormalities?
    Olajumoke A. Morenikeji, Omotayo S. Atanda, Ituna E. Eleng, Oyetunde T. Salawu
    Pediatric Infectious Disease.2014; 6(4): 124.     CrossRef
  • Malarial infection among antenatal and maternity clinics attendees at the Federal Medical Centre, Makurdi, Benue State, Nigeria
    Elizabeth Amuta, Robert Houmsou, Emmanuel Wama, Mary Ameh
    Infectious Disease Reports.2014; 6(1): 5050.     CrossRef
  • Comorbidities and Lack of Blood Transfusion May Negatively Affect Maternal Outcomes of Women with Obstetric Hemorrhage Treated with NASG
    Alison El Ayadi, Sarah Raifman, Farouk Jega, Elizabeth Butrick, Yemisi Ojo, Stacie Geller, Suellen Miller, Roger C. Young
    PLoS ONE.2013; 8(8): e70446.     CrossRef
  • Prevalence of Congenital Malaria in Minna, North Central Nigeria
    Innocent Chukwuemeka James Omalu, Charles Mgbemena, Amaka Mgbemena, Victoria Ayanwale, Israel Kayode Olayemi, Adeniran Lateef, Victoria I. Chukwuemeka
    Journal of Tropical Medicine.2012; 2012: 1.     CrossRef
  • Parasitologic Assessment of Two-Dose and Monthly Intermittent Preventive Treatment of Malaria during Pregnancy with Sulphadoxine-Pyrimethamine (IPTP-SP) in Lagos, Nigeria
    Chimere O. Agomo, Wellington A. Oyibo, Funke Odukoya-Maije
    Malaria Research and Treatment.2011; 2011: 1.     CrossRef
  • Use and Effects of Malaria Control Measures in Pregnancy in Lagos, Nigeria
    Michael Efunshile, A. O. J. Amoo, Grace B. Akintunde, Oluwole D. Ojelekan, Wolfgang König, Brigitte König
    The Korean Journal of Parasitology.2011; 49(4): 365.     CrossRef
  • Prevalence of Dihydrofolate Reductase Gene Mutations in Plasmodium falciparum Isolate from Pregnant Women in Nigeria
    Olusola Ojurongbe, Bukola D. Tijani, Adegboyega A. Fawole, Oluwaseyi A. Adeyeba, Juergen F. Kun
    Infectious Disease Reports.2011; 3(2): e16.     CrossRef
  • A study of anemia in women with asymptomatic malaria parasitaemia at their first antenatal care visit at the General Hospital, Ikot Ekpene, Akwa Ibom State, Nigeria
    EI Ekanem, TU Agan, EE Efiok, MI Ekott, E Okodi
    Asian Pacific Journal of Tropical Medicine.2010; 3(7): 567.     CrossRef
  • A Serosurvey of Blood Parasites (Plasmodium, Microfilaria, HIV, HBsAG, HCV Antibodies) in Prospective Nigerian Blood Donors
    J. A. Alli, I. O. Okonko, O. A. Abraham, A. F. Kolade, P.N. Ogunjobi, A. O. Salako, M. O. Ojezele, J. C. Nwanze
    Research Journal of Medical Sciences.2010; 4(4): 255.     CrossRef
  • 14,585 View
  • 282 Download
  • Crossref

Original Article

Serum Antigen and Antibody Detection in Echinococcosis: Application in Serodiagnosis of Human Hydatidosis
Seyed Mahmoud Sadjjadi, Farzaneh Sedaghat, Seyed Vahid Hosseini, Bahador Sarkari
Korean J Parasitol 2009;47(2):153-157.
Published online May 27, 2009
DOI: https://doi.org/10.3347/kjp.2009.47.2.153

Diagnosis of hydatidosis is based on immunodiagnostic methods along with radiological and ultrasound examinations. The
objective
s of the present study were to develop a specific and simple antigen-based ELISA method for diagnosis of hydatidosis and compare it with antibody detection method. The subjects in this study included 89 patients in the following groups: surgically confirmed hydatidosis patients (35 cases), control with other parasitic diseases (29 cases), and healthy controls (25 cases). Hyperimmune serum was raised against hydatid cyst fluid in rabbits. Anti-hydatid cyst IgG was purified by affinity chromatography using protein A column and labeled with horseradish peroxidase. Collected sera were assessed for hydatid cyst antigens and antibody by ELISA. Circulating hydatid antigen was found in 9 out of 35 patients with surgically confirmed hydatidosis. A sensitivity of 25.7% and a specificity of 98.0% were calculated for the antigen detection assay. Antibody detection by indirect ELISA, using antigen B, showed that 94.2% of patients (33 cases) have anti-hydatid cyst antibodies in their serum while cross reaction was noted in a few of non-hydatidosis patients. A sensitivity of 94.2% and specificity of 81.6% were found for the antibody detection assay. Findings of this study indicated that antibody detection assay is a sensitive approach for diagnosis of hydatid cyst while antigen detection assay might be a useful approach for assessment of the efficacy of treatment especially after removal of the cyst.

Citations

Citations to this article as recorded by  Crossref logo
  • Current challenges and future prospects in patients with recurrent cystic echinococcosis; an updated mini review
    Nayer Mehdizad Bakhtiar, Mahmoud Mahami-Oskouei, Ehsan Ahmadpour, Mohammad Hasan Kohansal, Adel Spotin
    Experimental Parasitology.2025; 277: 109028.     CrossRef
  • Human and camel cystic echinococcosis – a polyclonal antibody-based sandwich ELISA for its serodiagnosis with molecular identification
    A. Maher, N. I. Toaleb, R. M. Shaapan, D. Aboelsoued, M. B. Salman, S. Zaky
    Veterinary Research Communications.2024; 48(4): 2193.     CrossRef
  • Proteomics investigation of human sera for determination of postoperative indicators of pulmonary cystic echinococcosis
    Fatemeh Sadat Sadjjadi, Homa Hajjaran, Bahareh Sedaghat, Parviz Mardani, Seyed Mahmoud Sadjjadi
    Journal of Cardiothoracic Surgery.2023;[Epub]     CrossRef
  • Basic Operative Tactics for Pulmonary Echinococcosis in the Era of Endostaplers and Energy Devices
    Estera Bakinowska, Konstantinos Kostopanagiotou, Małgorzata Edyta Wojtyś, Kajetan Kiełbowski, Konrad Ptaszyński, Darko Gajić, Nikola Ruszel, Janusz Wójcik, Tomasz Grodzki, Periklis Tomos
    Medicina.2023; 59(3): 543.     CrossRef
  • Molecular characterization and serodiagnostic evaluation of the Echinococcus ortleppi recombinant glutaredoxin 1 protein for cystic echinococcosis in buffalo (Bubalus bubalis)
    K.A. Yashica, S. Samanta, R. Balaji, V. Jawalagatti, M. Silamparasan, S. Anandu, A. Rialch, S.C. Gupta, Anup Kumar Tewari
    Veterinary Parasitology.2023; 319: 109941.     CrossRef
  • Determination of echinococcosis IgG antibodies using magnetic bead-based chemiluminescence immunoassay
    Cuicui Chen, Huankun Liang, Fenglan Peng, Shuhai Zhong, Yanhong Lu, Guiling Guo, Laiqing Li
    Journal of Immunological Methods.2023; 520: 113513.     CrossRef
  • A Novel Designed Sandwich ELISA for the Detection of Echinococcus granulosus Antigen in Camels for Diagnosis of Cystic Echinococcosis
    Nagwa I. Toaleb, Dina Aboelsoued, Kadria N. Abdel Megeed, Sahar Hussein Abdalla Hekal
    Tropical Medicine and Infectious Disease.2023; 8(8): 400.     CrossRef
  • Intramuscular hydatid cyst of paraspinal muscle: A diagnostic challenge
    Anisha Shrestha, Anish Kumar Shrestha, Alok Deo, Gopal Raman Sharma
    Clinical Case Reports.2023;[Epub]     CrossRef
  • Voltammetric Label‐free Immunosensors for the Diagnosis of Cystic Echinococcosis
    Shimaa Eissa, Rahmah Noordin, Mohammed Zourob
    Electroanalysis.2020; 32(6): 1170.     CrossRef
  • Co-existence of hepatocellular carcinoma and cystic echinococcosis
    Ran Bo, Aimaiti Yasen, Yingmei Shao, Wenbao Zhang, Renyong Lin, Tiemin Jiang, Hao Wen, Hui Xiao, Tuerganaili Aji
    Infectious Agents and Cancer.2020;[Epub]     CrossRef
  • The clinical and cytomorphological spectrum of hydatid disease
    Gargi Kapatia, Jesty P. Tom, Manish Rohilla, Parikshaa Gupta, Nalini Gupta, Radhika Srinivasan, Arvind Rajwanshi, Pranab Dey
    Diagnostic Cytopathology.2020; 48(6): 547.     CrossRef
  • Targeted Sequencing of Genomic Repeat Regions Detects Circulating Cell-free Echinococcus DNA
    Zhengqing Wan, Xiaoqing Peng, Lu Ma, Qingshan Tian, Shizheng Wu, Junqi Li, Jie Ling, Weigang Lv, Binrong Ding, Jieqiong Tan, Zhuohua Zhang, Klaus Brehm
    PLOS Neglected Tropical Diseases.2020; 14(3): e0008147.     CrossRef
  • Serodiagnosis of human cystic echinococcosis based on recombinant antigens B8/1 and B8/2 of Echinococcus granulosus
    Seyyed Hossein Khatami, Mortaza Taheri-Anganeh, Ahmad Movahedpour, Amir Savardashtaki, Amin Ramezani, Bahador Sarkari, Zohreh Mostafavi-Pour
    Journal of Immunoassay and Immunochemistry.2020; 41(6): 1010.     CrossRef
  • Lateral flow dipstick antigen assay for human cystic echinococcosis
    Sam Khanbabaie, Mehdi Riazi, Chiat Han Chang, Muhammad Hafiznur Yunus, Rahmah Noordin
    Acta Tropica.2019; 190: 171.     CrossRef
  • Seroepidemiological study of cystic echinococcosis in nomadic communities in the southwest of Iran: A population-based study
    Abdolali Moshfe, Bahador Sarkari, Nasir Arefkhah, Reza Nikbakht, Reza Shahriarirad, Zahra Rezaei, Ali Jamshidi, Farid Moradian
    Journal of Immunoassay and Immunochemistry.2019; 40(2): 183.     CrossRef
  • Comparison of Sensitivity and Specificity of Native ELISA Test (Prepared in Khouzestan, Iran) and Commercial ELISA Kit in the Diagnosis of Human Hydatidosis
    Maryam Fasihi Karami, Sharif Maraghi, Abdollah Rafiei, Seyed Mahmoud Latifi, Gholam Abbas Kaydani
    Zahedan Journal of Research in Medical Sciences.2019;[Epub]     CrossRef
  • In Vitro Study on Protoscolicidal Effect of Methanolic Extract of Allium hirtifolium on Protoscoleces of Cystic Echinococcosis
    Z. Shahamir Tabatabaei, S. Dehshahri, M.M. Taghi, F. Esfandiari, F.S. Sadjjadi, M. Ebrahimipour, S.M. Sadjjadi
    Infectious Disorders - Drug Targets.2019; 19(3): 264.     CrossRef
  • DNA extraction from hydatid cyst protoscolices: Comparison of five different methods
    Afshin Barazesh, Bahador Sarkari, Sepideh Ebrahimi, Mehdi Hami
    Veterinary World.2018; 11(2): 231.     CrossRef
  • Seroprevalence of Hydatidosis in Kaboodarahang, Hamadan Province, Iran, in 2016 - 2017
    Rostam Barati, Khojasteh Sharifi-Sarasiabi, Yaghoob Hamedi, Mohammad Matini, Jebreil Shamseddin
    Hormozgan Medical Journal.2018; 22(4): e86498.     CrossRef
  • Seroprevalence of cystic echinococcosis in blood donors in Fars province, southern Iran
    Bahador Sarkari, Farshid Hosseini, Samaneh Abdolahi Khabisi, Farzaneh Sedaghat
    Parasite Epidemiology and Control.2017; 2(1): 8.     CrossRef
  • Evaluation of purified 27.5 kDa protoscolex antigen-based ELISA for the detection of circulating antigens and antibodies in sheep and human hydatidosis
    I.R. Bauomi, A.M. El-Amir, A.M. Fahmy, R.S. Zalat, T.M. Diab
    Journal of Helminthology.2015; 89(5): 577.     CrossRef
  • Diagnostic puzzle: Can you decipher by imaging only the nature of the cystic pancreatic lesion that is described below?
    Andriana Kouloura, G. Sourtse, A. Pintireki, S. Peristeraki, K. Karkoulias, S. Lanitis, G. Sgourakis, P. Brotzakis, C. Karaliotas
    Hellenic Journal of Surgery.2015; 87(3): 258.     CrossRef
  • Comparative Evaluation of Different Diagnostic Techniques using Laminated Layer Antigen for Serodiagnosis of Human Hydatidosis
    Amany A. Rady, Bahaa El Deen W. El Aswa, Bassam M. Masoud
    Research Journal of Parasitology.2014; 9(2): 41.     CrossRef
  • Diagnostics of Echinococcus granulosus particles in hepatic cysts punctate of seropositive patients
    T. Skuhala, D. Stoj?evi? Jan, B. Desnica
    Helminthologia.2014;[Epub]     CrossRef
  • Lateral Flow Test Using Echinococcus granulosus Native Antigen B and Comparison of IgG and IgG4 Dipsticks for Detection of Human Cystic Echinococcosis
    Sabariah Osman, Akbar Khalilpour, Rahmah Noordin, Seyed Mahmoud Sadjjadi, Muhammad Hafiznur Yunus, Zohreh Kazemi Moghadam, Nor Dyana Zakaria
    The American Journal of Tropical Medicine and Hygiene.2014; 91(5): 994.     CrossRef
  • Serodiagnosis of human hydatidosis with an ELISA developed based on antigens derived from sheep hydatid cysts and comparison with a commercial human ELISA kit
    S Fotoohi, G.R Hashemi Tabar, H Borji
    Asian Pacific Journal of Tropical Medicine.2013; 6(9): 723.     CrossRef
  • Using specific synthetic peptide (p176) derived AgB 8/1-kDa accompanied by modified patient’s sera: A novel hypothesis to follow-up of Cystic echinococcosis after surgery
    Soheila Rouhani, Parviz Parvizi, Adel Spotin
    Medical Hypotheses.2013; 81(4): 557.     CrossRef
  • Extrahepatic Primary Adrenal Alveolar Echinococcosis: A Review
    Zhi-gang Chu, Fa-jin Lv, Zhi-yu Zhu, Yu Ouyang
    Surgical Infections.2013; 14(4): 418.     CrossRef
  • Evaluation of rabbit antibody response against 8 and 16 kDa recombinant subunits of antigen B from Echinococcus granulosus
    Jahangir Abdi, Bahram Kazemi, Mohammad Hasan Karimfar, Mohammad Bagher Rokni
    Asian Pacific Journal of Tropical Medicine.2012; 5(5): 355.     CrossRef
  • Serodiagnosis of sheep hydatidosis with hydatid fluid, protoscolex, and whole body of Echinococcus granulosus antigens
    Gholamreza Hashemi Tabar, Alireza Haghparast, Hassan Borji
    Comparative Clinical Pathology.2012; 21(4): 429.     CrossRef
  • 10,315 View
  • 112 Download
  • Crossref
Mini Review
Malaria Diagnosis: A Brief Review
Noppadon Tangpukdee, Chatnapa Duangdee, Polrat Wilairatana, Srivicha Krudsood
Korean J Parasitol 2009;47(2):93-102.
Published online May 26, 2009
DOI: https://doi.org/10.3347/kjp.2009.47.2.93

Malaria is a major cause of death in tropical and sub-tropical countries, killing each year over 1 million people globally; 90% of fatalities occur in African children. Although effective ways to manage malaria now exist, the number of malaria cases is still increasing, due to several factors. In this emergency situation, prompt and effective diagnostic methods are essential for the management and control of malaria. Traditional methods for diagnosing malaria remain problematic; therefore, new technologies have been developed and introduced to overcome the limitations. This review details the currently available diagnostic methods for malaria.

Citations

Citations to this article as recorded by  Crossref logo
  • From Plants to Pills: Malaria Treatment Advancements in India
    Navpreet Kaur, Jhilli Basu, Shanu Raina, Sana Sood, Diksha Chauhan, Priya Jaswal
    Anti-Infective Agents.2025;[Epub]     CrossRef
  • Impact of estimated glomerular filtration rate (eGFR) on in-hospital mortality: an age- and HIV status-specific retrospective cohort study in Uganda
    Odong Christopher, Wang Yanmei, Makabayi Emmanuel Yeko, Doreen Mary Nanyunja, Kuule Julius Kabbali
    BMC Nephrology.2025;[Epub]     CrossRef
  • A 5G network based conceptual framework for real-time malaria parasite detection from thick and thin blood smear slides using modified YOLOv5 model
    Swati Lipsa, Ranjan Kumar Dash, Korhan Cengiz, Nikola Ivković, Adnan Akhunzada
    DIGITAL HEALTH.2025;[Epub]     CrossRef
  • Autofluorescence of Red Blood Cells Infected with P. falciparum as a Preliminary Analysis of Spectral Sweeps to Predict Infection
    Miguel A. Garrido-Tamayo, Alejandro Rincón Santamaría, Fredy E. Hoyos, Tamara González Vega, David Laroze
    Biosensors.2025; 15(2): 123.     CrossRef
  • The Diagnostic Performance of a Sysmex XN‐31 Automated Malaria Analyzer vs. Expert Microscopy
    S. Onsongo, K. Otieno, L. Mathenge, E. Makotsi, G. Kariuki, V. Ngetich, G. Muriithi, A. T. Harrison, T. Odawo, S. Kariuki
    International Journal of Laboratory Hematology.2025; 47(4): 613.     CrossRef
  • Infected and Noninfected Diseases Detection for Human Health Using Surface Plasmon Resonance Biosensors: A Review
    Rajeev Kumar, Lokendra Singh, S. Malathi
    IEEE Sensors Journal.2025; 25(7): 10556.     CrossRef
  • Identification of visible and near-infrared signature peaks for arboviruses and Plasmodium falciparum
    Brendon Goh, Ricardo J. Soares Magalhães, Silvia Ciocchetta, Wenjun Liu, Maggy T. Sikulu-Lord, Raquel Inocencio da Luz,
    PLOS ONE.2025; 20(4): e0321362.     CrossRef
  • Off-grid field-deployable molecular diagnostic platform for malaria surveillance
    Madhavinadha Prasad Kona, Armel N. Tedjou, Mary Kefi, Francesco Buongiorno, Charles S. Wondji, George Dimopoulos
    Parasites & Vectors.2025;[Epub]     CrossRef
  • Educational Case: Malaria
    Mitchell Guerin, Kristin Olson, Elham Vali Betts
    Academic Pathology.2025; 12(2): 100181.     CrossRef
  • Design of FBG-based optical biosensor for the detection of malaria
    L. Vincent Raj, Smitha Sasi, P. Rajeswari, B. R. Pushpa, Anju V. Kulkarni, Siddalingappagouda Biradar
    Journal of Optics.2025;[Epub]     CrossRef
  • An investigation of SPR based optical fiber sensor with U-shape channels for refractive index based detection of malaria pathogens
    Parthasarathi Das, Gayadhar Pradhan
    Journal of Optics.2025;[Epub]     CrossRef
  • Application of artificial intelligence for quantifying Plasmodium berghei in blood samples of infected mice
    Noha Talal Zelai
    Journal of Vector Borne Diseases.2025; 62(2): 233.     CrossRef
  • Lab-on-paper diagnostics for blood sample analysis: a review
    Sumit Malik, Joginder Singh, Vivek Chaudhry, Kajal Saini, Ritika, Ahmad Umar, Ahmed A. Ibrahim, Sotirios Baskoutas
    Microchimica Acta.2025;[Epub]     CrossRef
  • Tunable MIM - grating based SPR biosensor using metal-bismuth selenide (Bi2Se3)- silicon nitride (Si3N4) for dengue, malaria, glucose, and electrolyte detection with enhanced sensitivity
    Nishat Tasnim, Abu S M Mohsin
    Physica Scripta.2025; 100(7): 075570.     CrossRef
  • Comparative analysis of machine learning models for malaria detection using validated synthetic data: a cost-sensitive approach with clinical domain knowledge integration
    Gudi V. Chandra Sekhar, Chekol Alemu
    Scientific Reports.2025;[Epub]     CrossRef
  • Phase-Based Classification of Malaria-Infected Parasite Red Blood Cells using Digital Holographic Imaging
    Charlotte Kyeremah, Aditya S Paul, Daniel Haehn, Manoj T Duraisinghn, Chandra S Yelleswarapu
    Microscopy and Microanalysis.2025;[Epub]     CrossRef
  • Pathophysiological Associations and Measurement Techniques of Red Blood Cell Deformability
    Minhui Liang, Dawei Ming, Jianwei Zhong, Choo Sheriel Shannon, William Rojas-Carabali, Kajal Agrawal, Ye Ai, Rupesh Agrawal
    Biosensors.2025; 15(9): 566.     CrossRef
  • Congenital malaria in a neonate born in a malaria-endemic area: a case report
    Biniyam Demisse Andarge, Kebede Almaw
    Journal of Medical Case Reports.2025;[Epub]     CrossRef
  • FRACTIONAL OPTIMAL CONTROL FOR THE ANALYTICAL TREATMENT OF MALARIA MODEL
    MUHAMMAD NADEEM, MUSTAFA HABIB, AMAN WARIS, LOREDANA FLORENTINA IAMBOR, P. A. AZEEM HAFIZ, SHARIFAH E. ALHAZMI
    Fractals.2025;[Epub]     CrossRef
  • Malaria detection in early stage using optical biosensors
    Monika Goyal, Mohit Sharma
    Journal of Modern Optics.2025; : 1.     CrossRef
  • Antigenic determinant analysis of FIKK Kinase family to identify novel candidates for diagnosis of Plasmodium falciparum.
    M. Rajendra Prasad, D. Anil Kumar, Eena Dodwani, Sukhwinder Singh, Vishal Trivedi
    Microbial Pathogenesis.2025; : 108070.     CrossRef
  • Design of a highly sensitive SPR biosensor for rapid malaria detection based on zinc telluride and blue phosphorus/tungsten disulfide material
    Md. Al Amin Islam Utshob, Maymona Binte Juwel, Rawfarin Sabiha, Aminur Rahman, Safayat-Al Imam, Khandakar Mohammad Ishtiak
    Biosensors and Bioelectronics: X.2025; 27: 100709.     CrossRef
  • An effective microscopic model for plasmonic sensing of malaria
    A. S. Kiyumbi, M. S. Tame
    Advanced Metamaterials.2025;[Epub]     CrossRef
  • Gold, MXene, and graphene nanofilm-based surface plasmon resonance sensor for malaria detection
    Bhishma Karki, Amrindra Pal, Partha Sarkar, Arun Uniyal, Ram Bharos Yadav
    Journal of Optics.2024; 53(5): 4805.     CrossRef
  • Diagnostic value of rapid test for malaria among febrile neonates in a tertiary hospital in North-East Nigeria: a prospective cross-sectional study
    Yasangra Rabo Adeniji, Iliya Jalo, Ikechukwu Okonkwo, Mercy Raymond Poksireni, Mohammed Manga, Oghenebrume Wariri, Halima Abdulkarim Alhassan, Elon Isaac Warnow
    Archives of Disease in Childhood.2024; 109(1): 11.     CrossRef
  • Diagnosis and management of malaria in the intensive care unit
    George Akafity, Nicholas Kumi, Joyce Ashong
    Journal of Intensive Medicine.2024; 4(1): 3.     CrossRef
  • Breath biomarkers in Non-Carcinogenic diseases
    Pedro Catalão Moura, Maria Raposo, Valentina Vassilenko
    Clinica Chimica Acta.2024; 552: 117692.     CrossRef
  • Recent advances in the synthesis and antimalarial activity of 1,2,4-trioxanes
    Komal Rathi, Monika Shukla, Mohammad Hassam, Rahul Shrivastava, Varun Rawat, Ved Prakash Verma
    Bioorganic Chemistry.2024; 143: 107043.     CrossRef
  • The design, synthesis and antiplasmodial evaluation of novel sulfoximine-isoxazole hybrids as potential antimalarial agents
    Jackie L. Mabasa, Tommy F. Mabasa, Musawenkosi L. Nyathi, Paseka T. Moshapo
    European Journal of Medicinal Chemistry Reports.2024; 10: 100128.     CrossRef
  • The Laboratory Diagnosis of Malaria: A Focus on the Diagnostic Assays in Non-Endemic Areas
    Adriana Calderaro, Giovanna Piccolo, Carlo Chezzi
    International Journal of Molecular Sciences.2024; 25(2): 695.     CrossRef
  • COVID-19 in patients presenting with malaria-like symptoms at a primary healthcare facility in Accra, Ghana
    Issabella Asamoah, Mildred Adusei-Poku, Priscilla Vandyck-Sey, Allen Steele-Dadzie, Atta Senior Kuffour, Albert Turkson, Ivy Asantewaa Asante, Kantanka Addo-Osafo, Quaneeta Mohktar, Bright Adu, Yaw A. Afrane, Kwamena W. C. Sagoe, Sanjai Kumar
    PLOS ONE.2024; 19(2): e0298088.     CrossRef
  • The Malaria Burden: A South African Perspective
    Marissa Balmith, Charlise Basson, Sarel J. Brand, Jianbing Mu
    Journal of Tropical Medicine.2024; 2024: 1.     CrossRef
  • Factors affecting delays in seeking treatment among malaria patients during the pre-certification phase in China
    Lianyu Jia, Xiaoyu Chen, Zhanchun Feng, Shangfeng Tang, Da Feng
    Malaria Journal.2024;[Epub]     CrossRef
  • A SYSTEMATIC REVIEW ON MALARIA DISEASE AND ITS TREATMENTS FOCUS ON ARTEMETHER DRUG
    SWAPNIL D. PHALAK, VISHAL BODKE, VISHAL BODKE, SATISH PANDAV, MALOJI RANAWARE
    International Journal of Current Pharmaceutical Research.2024; : 1.     CrossRef
  • Supporting Malaria Diagnosis Using Deep Learning and Data Augmentation
    Kenia Hoyos, William Hoyos
    Diagnostics.2024; 14(7): 690.     CrossRef
  • A Review of Clinical Trials of Cancer and Its Treatment as a Vaccine
    Chandani Chandarana, Anuradha Tiwari
    Reviews on Recent Clinical Trials.2024; 19(1): 7.     CrossRef
  • A polarization independent highly sensitive metasurface-based biosensor for lab-on-chip applications
    Rummanur Rahad, Mohammad Ashraful Haque, Mahin Khan Mahadi, Md. Omar Faruque, Sheikh Mohd. Ta-Seen Afrid, Abu S.M. Mohsin, Abdullah Md Nazim Uddin Rahman Niaz, Rakibul Hasan Sagor
    Measurement.2024; 231: 114652.     CrossRef
  • An optimised YOLOv4 deep learning model for efficient malarial cell detection in thin blood smear images
    Dhevisha Sukumarran, Khairunnisa Hasikin, Anis Salwa Mohd Khairuddin, Romano Ngui, Wan Yusoff Wan Sulaiman, Indra Vythilingam, Paul Cliff Simon Divis
    Parasites & Vectors.2024;[Epub]     CrossRef
  • Highly Sensitive SPR Biosensor for Malaria Detection Employing ZnO, Fe2O3, and Black Phosphorous
    Nikhil Pratap Singh, Adarsh Chandra Mishra, Sapana Yadav, Pooja Lohia, D. K. Dwivedi, M. Khalid Hossain
    Plasmonics.2024; 20(2): 1029.     CrossRef
  • Factors associated with the timely diagnosis of malaria and the utilization of types of healthcare facilities: a retrospective study in the Republic of Korea
    HyunJung Kim, Sangwoo Tak, So-dam Lee, Seongwoo Park, Kyungwon Hwang
    Osong Public Health and Research Perspectives.2024; 15(2): 159.     CrossRef
  • Machine and deep learning methods in identifying malaria through microscopic blood smear: A systematic review
    Dhevisha Sukumarran, Khairunnisa Hasikin, Anis Salwa Mohd Khairuddin, Romano Ngui, Wan Yusoff Wan Sulaiman, Indra Vythilingam, Paul C.S. Divis
    Engineering Applications of Artificial Intelligence.2024; 133: 108529.     CrossRef
  • Mathematical modeling and simulation for malaria disease transmission using the CF fractional derivative
    A.S. Alqahtani, Sehrish Ramzan, Syeda Alishwa Zanib, Aqsa Nazir, Khalid Masood, M.Y. Malik
    Alexandria Engineering Journal.2024; 101: 193.     CrossRef
  • Towards the development of cost-effective point-of-care diagnostic tools for poverty-related infectious diseases in sub-Saharan Africa
    Benedict Ofori, Seth Twum, Silas Nkansah Yeboah, Felix Ansah, Kwabena Amofa Nketia Sarpong
    PeerJ.2024; 12: e17198.     CrossRef
  • Detection of Plasmodium knowlesi in whole blood samples with sandwich enzyme-linked immunosorbent assay (ELISA) using rhoptry-associated protein 1 specific polyclonal antibodies
    Wan Siti Maryam Wan Nazri, Lau Yee Ling, Cheong Fei Wen
    Journal of Vector Borne Diseases.2024; 61(2): 203.     CrossRef
  • Breath Biomarkers of Pediatric Malaria: Reproducibility and Response to Antimalarial Therapy
    Amalia Z Berna, X Rosalind Wang, Lucy B Bollinger, Josephine Banda, Patricia Mawindo, Tasha Evanoff, Diana L Culbertson, Karl Seydel, Audrey R Odom John
    The Journal of Infectious Diseases.2024;[Epub]     CrossRef
  • LIGAND-BASED VIRTUAL SCREENING OF FDA-APPROVED DRUGS TO IDENTIFY NEW INHIBITORS AGAINST LACTATE DEHYDROGENASE ENZYME OF MALARIA PARASITES
    HASANAIN ABDULHAMEED ODHAR, AHMED FADHIL HASHIM, SUHAD SAMI HUMADI, SALAM WAHEED AHJEL
    International Journal of Applied Pharmaceutics.2024; : 255.     CrossRef
  • Enhancing Gene Co-Expression Network Inference for the Malaria Parasite Plasmodium falciparum
    Qi Li, Katrina A. Button-Simons, Mackenzie A. C. Sievert, Elias Chahoud, Gabriel F. Foster, Kaitlynn Meis, Michael T. Ferdig, Tijana Milenković
    Genes.2024; 15(6): 685.     CrossRef
  • Au-Al2O3-Coated Highly Sensitive Broad-Range Refractive Index Sensor for Detecting Malaria Disease in Human Blood
    Sanjeev Mani Yadav
    IEEE Sensors Journal.2024; 24(15): 23754.     CrossRef
  • Exploring the intricacies of malaria: Unveiling the biological nature of a persistent menace
    Nitin Rajan, Sapna Kumari, Amisha Kumari
    Journal of Pharmaceutical and Biological Sciences.2024; 12(1): 19.     CrossRef
  • Plasmodium falciparum genetic diversity; implications for malaria control in Ethiopia: Systematic review and meta‐analysis
    Zufan Y. Abriham, Aysheshim K. Belew, Lemlem D. Baffa, Berhanu Mengistu, Moges Gasahw, Esmeal A. Mohammod, Muluken C. Agimas, Mekonnen Sisay, Dessie A. Angaw
    Health Science Reports.2024;[Epub]     CrossRef
  • Numerical Simulation of a High Sensitivity Spr Sensor for Rapid Malaria Diagnosis using BP and Graphene 2D Materials
    Vinay Mohan, Amrindra Pal, Sandeep Sharma
    Plasmonics.2024; 20(7): 4715.     CrossRef
  • Non-Invasive Malaria Detection in Sub-Saharan Africa Using a DNA-Based Sensor System
    Trine Juul-Kristensen, Celine Thiesen, Line Wulff Haurum, Josephine Geertsen Keller, Romeo Wenceslas Lendamba, Rella Zoleko Manego, Madeleine Eunice Betouke Ongwe, Birgitta Ruth Knudsen, Eduardo Pareja, Eduardo Pareja-Tobes, Rodrigo Labouriau, Ghyslain Mo
    Sensors.2024; 24(24): 7947.     CrossRef
  • Molecular surveillance of Plasmodium falciparum histidine-rich protein 2/3 gene deletions in Mozambique, 2023
    Clemente da Silva, Dário Tembisse, Pau Cisteró, Eduard Rovira-Vallbona, Neide Canana, Paulino da Costa, Gloria Matambisso, Andrés Aranda-Díaz, Henriques Mbeve, Nelo Ndimande, Alcido Timana, Aura Hunguana, Simone Boene, Arnau Pujol, Bernardete Rafael, Brya
    Malaria Journal.2024;[Epub]     CrossRef
  • Comparison of fine-scale malaria strata derived from population survey data collected using RDTs, microscopy and qPCR in South-Eastern Tanzania
    Issa H. Mshani, Frank M. Jackson, Elihaika G. Minja, Said Abbasi, Nasoro S. Lilolime, Faraja E. Makala, Alfred B. Lazaro, Idrisa S. Mchola, Linda N. Mukabana, Najat F. Kahamba, Alex J. Limwagu, Rukia M. Njalambaha, Halfan S. Ngowo, Donal Bisanzio, Frances
    Malaria Journal.2024;[Epub]     CrossRef
  • Semi-supervised graph learning framework for apicomplexan parasite classification
    Yan Ha, Xiangjie Meng, Zeyu Du, Junfeng Tian, Yu Yuan
    Biomedical Signal Processing and Control.2023; 81: 104502.     CrossRef
  • Sensing and Detection Capabilities of One-Dimensional Defective Photonic Crystal Suitable for Malaria Infection Diagnosis from Preliminary to Advanced Stage: Theoretical Study
    Sujit Kumar Saini, Suneet Kumar Awasthi
    Crystals.2023; 13(1): 128.     CrossRef
  • Assessing the knowledge and practices of primary healthcare workers on malaria diagnosis and related challenges in view of COVID-19 outbreak in a Nigerian Southwestern metropolis
    Esther Oluwayemisi Ayandipo, Deborah Babatunde, Oladipo Afolayan, Olabisi Kalejaye, Taiwo Obembe, Javier H Eslava-Schmalbach
    PLOS Global Public Health.2023; 3(1): e0000625.     CrossRef
  • SARS-CoV-2 and Plasmodium falciparum coinfection: a case report
    Sanja Mandić, Luka Švitek, Tara Rolić, Iva Lukić, Dubravka Lišnjić, Mario Duvnjak, Ivana Sarić, Vatroslav Šerić
    Infectious Diseases.2023; 55(4): 299.     CrossRef
  • A high‐performance cell‐phone based polarized microscope for malaria diagnosis
    Zhenfang Yu, Yunfei Li, Lin Deng, Bing Luo, Pinghui Wu, Dongxian Geng
    Journal of Biophotonics.2023;[Epub]     CrossRef
  • Current developments on the antimalarial, antileishmanial, and antitrypanosomal potential and mechanisms of action of Terminalia spp.
    Mariscal Brice Tchatat Tali, Boniface Pone Kamdem, Jean Claude Tchouankeu, Fabrice Fekam Boyom
    South African Journal of Botany.2023; 156: 309.     CrossRef
  • Malaria therapeutics: are we close enough?
    Himani Tripathi, Preshita Bhalerao, Sujeet Singh, Hemant Arya, Bader Saud Alotaibi, Summya Rashid, Mohammad Raghibul Hasan, Tarun Kumar Bhatt
    Parasites & Vectors.2023;[Epub]     CrossRef
  • Knowledge and practice of malaria prevention among residents of Ratuwamai Municipality, Nepal
    Rajesh Karki, Niruta Bartoula, Maheshor Kaphle, Sanjaya Kumar Shah
    One Health Bulletin.2023;[Epub]     CrossRef
  • Study of Disease Dynamics of Co-infection of Rotavirus and Malaria with Control Strategies
    I. Ratti, P. Kalra
    Malaysian Journal of Mathematical Sciences.2023; 17(2): 151.     CrossRef
  • Metallic Nanoparticles and Core-Shell Nanosystems in the Treatment, Diagnosis, and Prevention of Parasitic Diseases
    Grzegorz Król, Kamila Fortunka, Michał Majchrzak, Ewelina Piktel, Paulina Paprocka, Angelika Mańkowska, Agata Lesiak, Maciej Karasiński, Agnieszka Strzelecka, Bonita Durnaś, Robert Bucki
    Pathogens.2023; 12(6): 838.     CrossRef
  • Impact of malaria diagnostic choice on monitoring of Plasmodium falciparum prevalence estimates in the Democratic Republic of the Congo and relevance to control programs in high-burden countries
    Alpha Oumar Diallo, Kristin Banek, Melchior Mwandagalirwa Kashamuka, Joseph Alexandre Mavungu Bala, Marthe Nkalani, Georges Kihuma, Tommy Mambulu Nseka, Joseph Losoma Atibu, Georges Emo Mahilu, Lauren McCormick, Samuel J. White, Rachel Sendor, Cyrus Sinai
    PLOS Global Public Health.2023; 3(7): e0001375.     CrossRef
  • Medicinal Chemistry Approaches for the Discovery of Plasmodium Falciparum Dihydroorotate Dehydrogenase Inhibitors as Antimalarial Agents
    Vivek K Vyas, Tanvi Shukla, Manmohan Sharma
    Future Medicinal Chemistry.2023; 15(14): 1295.     CrossRef
  • Evaluation of an automated microscope using machine learning for the detection of malaria in travelers returned to the UK
    Roxanne R. Rees-Channer, Christine M. Bachman, Lynn Grignard, Michelle L. Gatton, Stephen Burkot, Matthew P. Horning, Charles B. Delahunt, Liming Hu, Courosh Mehanian, Clay M. Thompson, Katherine Woods, Paul Lansdell, Sonal Shah, Peter L. Chiodini
    Frontiers in Malaria.2023;[Epub]     CrossRef
  • An Efficient and Effective Framework for Intestinal Parasite Egg Detection Using YOLOv5
    Satish Kumar, Tasleem Arif, Gulfam Ahamad, Anis Ahmad Chaudhary, Salahuddin Khan, Mohamed A. M. Ali
    Diagnostics.2023; 13(18): 2978.     CrossRef
  • Reflections on the surge in malaria cases after unprecedented flooding in Pakistan—A commentary
    Shehroze Tabassum, Tuaseen Kalsoom, Zaofashan Zaheer, Aroma Naeem, Ahmed Afifi, Laya Ohadi
    Health Science Reports.2023;[Epub]     CrossRef
  • Linear and Nonlinear Associations between Meteorological Variables and the Incidence of Malaria in Zahedan District Southwest of Iran 2000-2019
    Sairan Nili, Narges Khanjani, Ebrahim Ghaderi, Minoo Mohammadkhani
    The Open Public Health Journal.2023;[Epub]     CrossRef
  • Key considerations, target product profiles, and research gaps in the application of infrared spectroscopy and artificial intelligence for malaria surveillance and diagnosis
    Issa H. Mshani, Doreen J. Siria, Emmanuel P. Mwanga, Bazoumana BD. Sow, Roger Sanou, Mercy Opiyo, Maggy T. Sikulu-Lord, Heather M. Ferguson, Abdoulaye Diabate, Klaas Wynne, Mario González-Jiménez, Francesco Baldini, Simon A. Babayan, Fredros Okumu
    Malaria Journal.2023;[Epub]     CrossRef
  • A Novel Deep Learning Approach to Malaria Disease Detection on Two Malaria Datasets
    İbrahim ÇETİNER, Halit ÇETİNER
    Bilecik Şeyh Edebali Üniversitesi Fen Bilimleri Dergisi.2023; 10(2): 254.     CrossRef
  • Oxidation of chloroquine drug by ferrate: Kinetics, reaction mechanism and antibacterial activity
    Feilong Dong, Jinzhe Li, Qiufeng Lin, Da Wang, Cong Li, Yi Shen, Tao Zeng, Shuang Song
    Chemical Engineering Journal.2022; 428: 131408.     CrossRef
  • Genotyping of ABO and Duffy blood groups among malaria patients in Thailand
    Phattharaphon Hongfongfa, Jiraporn Kuesap
    Journal of Parasitic Diseases.2022; 46(1): 178.     CrossRef
  • Extrinsic parameter's adjustment and potential implications in Plasmodium falciparum malaria diagnosis
    Vijayalakshmi A, Rajesh Kanna B, Vijayalakshmi C
    Microscopy Research and Technique.2022; 85(2): 685.     CrossRef
  • Care-seeking delay of imported malaria to China: implications for improving post-travel healthcare for migrant workers
    Guangyu Lu, Yuanyuan Cao, Qi Chen, Guoding Zhu, Olaf Müller, Jun Cao
    Journal of Travel Medicine.2022;[Epub]     CrossRef
  • A generalized deep learning-based framework for assistance to the human malaria diagnosis from microscopic images
    Ziheng Yang, Halim Benhabiles, Karim Hammoudi, Feryal Windal, Ruiwen He, Dominique Collard
    Neural Computing and Applications.2022; 34(17): 14223.     CrossRef
  • Analysis of malaria clinical−epidemiological predictors in individuals from Brazilian Amazon
    Paulo Guilherme Souza Lisbôa, Janaina Maria Rodrigues Medeiros, Arthur Vinícius de Souza, Bruno Fernando Barros dos Santos, Henrique Otávio Coutinho Sanches, Juliane Lúcia Gomes da Rocha, Wender de Jesus Pena Correa Junior, Gabriela Góes Costa, Tania do S
    Parasitology.2022; 149(1): 10.     CrossRef
  • A Novel Data Augmentation Convolutional Neural Network for Detecting Malaria Parasite in Blood Smear Images
    David Opeoluwa Oyewola, Emmanuel Gbenga Dada, Sanjay Misra, Robertas Damaševičius
    Applied Artificial Intelligence.2022;[Epub]     CrossRef
  • Recent progress in electrochemical sensors for detection and quantification of malaria
    Zondi Nate, Atal A.S. Gill, Ruchika Chauhan, Rajshekhar Karpoormath
    Analytical Biochemistry.2022; 643: 114592.     CrossRef
  • Review of Microdevices for Hemozoin-Based Malaria Detection
    Vitória Baptista, Weng Kung Peng, Graça Minas, Maria Isabel Veiga, Susana O. Catarino
    Biosensors.2022; 12(2): 110.     CrossRef
  • Five-Year Trend of Malaria Prevalence in Mojo Town, Central Ethiopia: Shifting Burden of the Disease and Its Implication for Malaria Elimination: A Retrospective Study
    Andargie Abate, Mesfin Assefa, Lemu Golassa
    Infection and Drug Resistance.2022; Volume 15: 455.     CrossRef
  • Deep learning for microscopic examination of protozoan parasites
    Chi Zhang, Hao Jiang, Hanlin Jiang, Hui Xi, Baodong Chen, Yubing Liu, Mario Juhas, Junyi Li, Yang Zhang
    Computational and Structural Biotechnology Journal.2022; 20: 1036.     CrossRef
  • ABO blood group and risk of malaria during pregnancy: a systematic review and meta-analysis
    Ling Ai, Jingyuan Li, Wenjun Wang, Yuying Li
    Epidemiology and Infection.2022;[Epub]     CrossRef
  • MiRNA: Biological Regulator in Host-Parasite Interaction during Malaria Infection
    Poonam Kataria, Neha Surela, Amrendra Chaudhary, Jyoti Das
    International Journal of Environmental Research and Public Health.2022; 19(4): 2395.     CrossRef
  • Can malaria parasites be spontaneously cleared?
    Merryn S. Roe, Katherine O’Flaherty, Freya J.I. Fowkes
    Trends in Parasitology.2022; 38(5): 356.     CrossRef
  • Malaria diagnostic update: From conventional to advanced method
    Loeki Enggar Fitri, Tarina Widaningrum, Agustina Tri Endharti, Muhammad Hatta Prabowo, Nuning Winaris, Rivo Yudhinata Brian Nugraha
    Journal of Clinical Laboratory Analysis.2022;[Epub]     CrossRef
  • Current methods for the detection of Plasmodium parasite species infecting humans
    Lucinda Slater, Shoaib Ashraf, Osama Zahid, Qasim Ali, Muhammad Oneeb, Muhammad Haroon Akbar, Muhammad Ilyas Riaz, Kiran Afshan, Neil Sargison, Umer Chaudhry
    Current Research in Parasitology & Vector-Borne Diseases.2022; 2: 100086.     CrossRef
  • Impact of Malaria Diagnostic Technologies on the Disease Burden in the Sub-Saharan Africa
    Josephine Wambani, Patrick Okoth, Linda Amoah
    Journal of Tropical Medicine.2022; 2022: 1.     CrossRef
  • Modeling of High-Performance SPR Refractive Index Sensor Employing Novel 2D Materials for Detection of Malaria Pathogens
    Abinash Panda, Puspa Devi Pukhrambam
    IEEE Transactions on NanoBioscience.2022; 21(2): 312.     CrossRef
  • Computational Methods for Automated Analysis of Malaria Parasite Using Blood Smear Images: Recent Advances
    Shankar Shambhu, Deepika Koundal, Prasenjit Das, Vinh Truong Hoang, Kiet Tran-Trung, Hamza Turabieh, Zhongxu Hu
    Computational Intelligence and Neuroscience.2022; 2022: 1.     CrossRef
  • Malaria diagnostic methods with the elimination goal in view
    Olukunle O. Oyegoke, Leah Maharaj, Oluwasegun P. Akoniyon, Illiya Kwoji, Alexandra T. Roux, Taiye S. Adewumi, Rajendra Maharaj, Bolanle T. Oyebola, Matthew A. Adeleke, Moses Okpeku
    Parasitology Research.2022; 121(7): 1867.     CrossRef
  • Plasmodium knowlesi: the game changer for malaria eradication
    Wenn-Chyau Lee, Fei Wen Cheong, Amirah Amir, Meng Yee Lai, Jia Hui Tan, Wei Kit Phang, Shahhaziq Shahari, Yee-Ling Lau
    Malaria Journal.2022;[Epub]     CrossRef
  • Highly sensitive photonic crystal fiber-based plasmonic biosensor with improved malaria detection application
    Bahar Meshginqalam, Jamal Barvestani
    The European Physical Journal Plus.2022;[Epub]     CrossRef
  • Willingness to accept malaria vaccine among caregivers of under-5 children in Southwest Ethiopia: a community based cross-sectional study
    Getachew Asmare
    Malaria Journal.2022;[Epub]     CrossRef
  • Physiologically-Based Pharmacokinetics Modeling for Hydroxychloroquine as a Treatment for Malaria and Optimized Dosing Regimens for Different Populations
    Jingchen Zhai, Beihong Ji, Lianjin Cai, Shuhan Liu, Yuchen Sun, Junmei Wang
    Journal of Personalized Medicine.2022; 12(5): 796.     CrossRef
  • Visible microspectrophotometry coupled with machine learning to discriminate the erythrocytic life cycle stages of P. falciparum malaria parasites in functional single cells
    John A. Adegoke, Hannah Raper, Callum Gassner, Philip Heraud, Bayden R. Wood
    The Analyst.2022; 147(12): 2662.     CrossRef
  • Surveillance of Viral Hemorrhagic Fever Viruses in Lassa Fever Suspects in Ondo State, Nigeria
    Azuka Patrick Okwuraiwe, Oumar Faye, Fehintola Anthonia Ige, Ayorinde Babatunde James, Joseph Ojonugwa Shaibu, Martin Faye, Olufemi Samuel Amoo, Oumar NDiaye, Olumuyiwa Babalola Salu , Sunday Aremu Omilabu, Rosemary Ajuma Audu
    European Journal of Medical and Health Sciences.2022; 4(3): 78.     CrossRef
  • Malaria Endemicity in the Rural Communities of Ebonyi State, Nigeria
    David Ekene Nwele, Ikechukwu Oliver Onyali, Milliam Okwudili Iwueze, Michael Okpara Elom, Ogbonna Elom Sabastian Uguru
    The Korean Journal of Parasitology.2022; 60(3): 173.     CrossRef
  • Potential Opportunities and Challenges of Deploying Next Generation Sequencing and CRISPR-Cas Systems to Support Diagnostics and Surveillance Towards Malaria Control and Elimination in Africa
    Beatus M. Lyimo, Zachary R. Popkin-Hall, David J. Giesbrecht, Celine I. Mandara, Rashid A. Madebe, Catherine Bakari, Dativa Pereus, Misago D. Seth, Ramadhan M. Ngamba, Ruth B. Mbwambo, Bronwyn MacInnis, Daniel Mbwambo, Issa Garimo, Frank Chacky, Sijenunu
    Frontiers in Cellular and Infection Microbiology.2022;[Epub]     CrossRef
  • Detection of Malaria Parasite Protein in Urine of Patients with Acute Uncomplicated Malaria Using Rapid Diagnostic Test Kits
    Amusan ABİODUN, Akinola OLUGBENGA, Akano KAZEEM, Gbotosho Grace OLUSOLA
    Journal of Microbiology and Infectious Diseases.2022; : 97.     CrossRef
  • Cerebral Malaria Presenting With Shock in an Adolescent: A Case Report
    Deborah Omoleye, Muhammad A Israr, Faria Tazin, Camille Celeste, Olanrewaju Saheed
    Cureus.2022;[Epub]     CrossRef
  • A microfluidic device for capturing malaria-infected red blood cells by magnetophoretic force using an array of V- and W-shaped nickel microstructures
    Pachara Noosawat, Werayut Srituravanich, Nattapol Damrongplasit, Yuji Suzuki, Morakot Kaewthamasorn, Alongkorn Pimpin
    Microfluidics and Nanofluidics.2022;[Epub]     CrossRef
  • KONVOLÜSYONEL SİNİR AĞI KULLANILARAK SITMA HASTALIĞI SINIFLANDIRILMASI
    İbrahim ÇETİNER
    Adıyaman Üniversitesi Mühendislik Bilimleri Dergisi.2022; 9(17): 273.     CrossRef
  • Comparative Assessment of Diagnostic Performance of Cytochrome Oxidase Multiplex PCR and 18S rRNA Nested PCR
    Preeti Kumari, Swati Sinha, Renuka Gahtori, Afshana Quadiri, Paras Mahale, Deepali Savargaonkar, Veena Pande, Bina Srivastava, Himmat Singh, Anupkumar R Anvikar
    The Korean Journal of Parasitology.2022; 60(4): 295.     CrossRef
  • Agreement among rapid diagnostic tests, urine malaria tests, and microscopy in malaria diagnosis of adult patients in southwestern Nigeria
    Jonathan Ayobami Oyeniyi, Ibrahim Sebutu Bello, Olanrewaju Oloyede Oyegbade, Azeez Oyemomi Ibrahim, Oyeladun Funmi Okunromade, Oladipupo Omolade Fakoya
    Journal of International Medical Research.2022;[Epub]     CrossRef
  • Deep Learning for Real-Time Malaria Parasite Detection and Counting Using YOLO-mp
    Anand Koirala, Meena Jha, Srinivas Bodapati, Animesh Mishra, Girija Chetty, Praveen Kishore Sahu, Sanjib Mohanty, Timir Kanta Padhan, Jyoti Mattoo, Ajat Hukkoo
    IEEE Access.2022; 10: 102157.     CrossRef
  • Grand challenges in major tropical diseases
    Beatriz Barreto-Duarte, Mariana Araújo-Pereira, João P. Miguez-Pinto, Isabella B. B. Ferreira, Rodrigo C. Menezes, Gabriela L. Rosier, Caian L. Vinhaes, Mateus Maggitti-Bezerril, Klauss Villalva-Serra, Bruno B. Andrade
    Frontiers in Tropical Diseases.2022;[Epub]     CrossRef
  • Phytochemical Analysis andIn vitroEvidence of Antimalarial, Antibacterial, Antifungal, Antioxidant and Anti-inflammatory Activities of Ethanol Extract ofEmblica officinalisFruit
    Jyoti Kaushik, Monu Yadav, Nidhi Sharma, Deepak K. Jindal, Kajal Joshi, Mini Dahiya, Aakash Deep
    Anti-Infective Agents.2022;[Epub]     CrossRef
  • Advances and challenges in automated malaria diagnosis using digital microscopy imaging with artificial intelligence tools: A review
    Carles Rubio Maturana, Allisson Dantas de Oliveira, Sergi Nadal, Besim Bilalli, Francesc Zarzuela Serrat, Mateu Espasa Soley, Elena Sulleiro Igual, Mercedes Bosch, Anna Veiga Lluch, Alberto Abelló, Daniel López-Codina, Tomàs Pumarola Suñé, Elisa Sayrol Cl
    Frontiers in Microbiology.2022;[Epub]     CrossRef
  • Application of machine and deep learning algorithms in optical microscopic detection of Plasmodium: A malaria diagnostic tool for the future
    Charles Ikerionwu, Chikodili Ugwuishiwu, Izunna Okpala, Idara James, Matthew Okoronkwo, Charles Nnadi, Ugochukwu Orji, Deborah Ebem, Anthony Ike
    Photodiagnosis and Photodynamic Therapy.2022; 40: 103198.     CrossRef
  • Elevated plasma α1-antichymotrypsin is a biomarker candidate for malaria patients
    Young Yil Bahk, Sang Bong Lee, Jong Bo Kim, Tong-Soo Kim, Sung-Jong Hong, Dong Min Kim, Sungkeun Lee
    BMB Reports.2022; 55(11): 571.     CrossRef
  • Profile and determinants of delayed care-seeking and diagnosis among patients with imported malaria: a retrospective study in China, 2014–2021
    Tao Zhang, Duoquan Wang, Yingjun Qian, Wei Ruan, Ying Liu, Jing Xia, Hui Yan, Yuan Sui, Shenning Lu, Xian Xu, Jingjing Jiang, Xiaofeng Lyu, Shuqi Wang, Shizhu Li, Weidong Li
    Infectious Diseases of Poverty.2022;[Epub]     CrossRef
  • Imported malaria with chikungunya co-infection: A case report
    Anupam Das, Manodeep Sen, Pranshu Pandey, Apurva Rautela, Haniya Jafar, Vikramjeet Singh, Jaya Garg, Jyotsna Agarwal
    IP International Journal of Medical Microbiology and Tropical Diseases.2022; 8(4): 342.     CrossRef
  • Tes Diagnostik Cepat Kadar Hemaglobin pada Penderita Infeksi Plasmodium di Puskesmas Doom, Sorong, Papua Barat
    Merlis Simon, Junaiddin Junaiddin, Fenti A Tupanwael
    Health Information : Jurnal Penelitian.2022; 14(2): 200.     CrossRef
  • Imported Malaria in an Immigrant Toddler Boy in Kashan, a Non-Malaria Endemic Area, Central Iran
    Tayebeh Taghipour, Mahzad Erami, Mojtaba Fakhrei, Hossein Hooshyar
    Journal of Medical Microbiology and Infectious Diseases.2022; 10(3): 149.     CrossRef
  • Malaria Parasite Detection Using a Quantum-Convolutional Network
    Javaria Amin, Muhammad Almas Anjum, Abida Sharif, Mudassar Raza, Seifedine Kadry, Yunyoung Nam
    Computers, Materials & Continua.2022; 70(3): 6023.     CrossRef
  • Exploring the combination characteristics of lumefantrine, an antimalarial drug and human serum albumin through spectroscopic and molecular docking studies
    Kabiru Abubakar Musa, Nor Farrah Wahidah Ridzwan, Saharuddin B. Mohamad, Saad Tayyab
    Journal of Biomolecular Structure and Dynamics.2021; 39(2): 691.     CrossRef
  • Synthesis and characterization of WO3-doped polyaniline to sense biomarker VOCs of Malaria
    P. Jisha, M. S. Suma, M. V. Murugendrappa
    Applied Nanoscience.2021; 11(1): 29.     CrossRef
  • Performance assessment of a widely used rapid diagnostic test CareStart™ compared to microscopy for the detection of Plasmodium in asymptomatic patients in the Western region of Cameroon
    Roland Bamou, Zidedine Nematchoua-Weyou, Michel Lontsi-Demano, Laura Gilberine Ningahi, Melanie Adèle Tchoumbou, Blaise Armand Defo-Talom, Marie Paul Audrey Mayi, Timoléon Tchuinkam
    Heliyon.2021; 7(2): e06271.     CrossRef
  • Modelling the impact of rapid diagnostic tests on Plasmodium vivax malaria in South Korea: a cost–benefit analysis
    Jung Ho Kim, Jiyeon Suh, Woon Ji Lee, Heun Choi, Jong-Dae Kim, Changsoo Kim, Jun Yong Choi, Ryeojin Ko, Heewon Kim, Jeehyun Lee, Joon Sup Yeom
    BMJ Global Health.2021; 6(2): e004292.     CrossRef
  • Malaria and the Heart
    Shyla Gupta, Naomi Gazendam, Juan María Farina, Clara Saldarriaga, Ivan Mendoza, Ricardo López-Santi, Gonzalo Emanuel Pérez, Manuel Martínez-Sellés, Adrian Baranchuk
    Journal of the American College of Cardiology.2021; 77(8): 1110.     CrossRef
  • Design and analysis of a single elliptical channel photonic crystal fiber sensor for potential malaria detection
    Araf Shafkat, Ahmed Nabih Zaki Rashed, Hazem M. El-Hageen, Aadel M. Alatwi
    Journal of Sol-Gel Science and Technology.2021; 98(1): 202.     CrossRef
  • Fully automated point-of-care differential diagnosis of acute febrile illness
    Sebastian Hin, Benjamin Lopez-Jimena, Mohammed Bakheit, Vanessa Klein, Seamus Stack, Cheikh Fall, Amadou Sall, Khalid Enan, Mohamed Mustafa, Liz Gillies, Viorel Rusu, Sven Goethel, Nils Paust, Roland Zengerle, Sieghard Frischmann, Manfred Weidmann, Konsta
    PLOS Neglected Tropical Diseases.2021; 15(2): e0009177.     CrossRef
  • Role of Platelet Indices as a Potential Marker for Malaria Severity
    Biruk Bayleyegn, Fikir Asrie, Aregawi Yalew, Berhanu Woldu, Francisco Gonzalez Salazar
    Journal of Parasitology Research.2021; 2021: 1.     CrossRef
  • Differential diagnosis of Plasmodium falciparum and Plasmodium vivax in mixed infection by colorimetric nanogold probes
    Nantawan Wangmaung, Sirinart Chomean, Wanida Ittarat
    Analytical Biochemistry.2021; 624: 114173.     CrossRef
  • A Near-Infrared “Matchbox Size” Spectrometer to Detect and Quantify Malaria Parasitemia
    John A. Adegoke, Kamila Kochan, Philip Heraud, Bayden R. Wood
    Analytical Chemistry.2021; 93(13): 5451.     CrossRef
  • Analytical validation of a real-time hydrolysis probe PCR assay for quantifying Plasmodium falciparum parasites in experimentally infected human adults
    Claire Y. T. Wang, Emma L. Ballard, Zuleima Pava, Louise Marquart, Jane Gaydon, Sean C. Murphy, David Whiley, Peter O’Rourke, James S. McCarthy
    Malaria Journal.2021;[Epub]     CrossRef
  • Assessment of Microscopic Detection of Malaria with Nested Polymerase Chain Reaction in War-Torn Federally Administered Tribal Areas of Pakistan
    Muhammad Faisal Nadeem, Aamer Ali Khattak, Nadia Zeeshan, Usman Ayub Awan, Adnan Yaqoob
    Acta Parasitologica.2021; 66(4): 1186.     CrossRef
  • Malaria Rapid Diagnostic Tests: Literary Review and Recommendation for a Quality Assurance, Quality Control Algorithm
    Michael J. Kavanaugh, Steven E. Azzam, David M. Rockabrand
    Diagnostics.2021; 11(5): 768.     CrossRef
  • OMNIGEN KIT ACCURACY FOR PLASMODIUM FALCIPARU
    Souléye lélo, Magatte Ndiaye, Khadim Sylla, Doudou Sow, Cheikh Binetou Fall, Aida Gaye, Issac Manga, Roger Tine, Babacar Faye
    GLOBAL JOURNAL FOR RESEARCH ANALYSIS.2021; : 156.     CrossRef
  • A Lab‐On‐chip Tool for Rapid, Quantitative, and Stage‐selective Diagnosis of Malaria
    Marco Giacometti, Francesca Milesi, Pietro Lorenzo Coppadoro, Alberto Rizzo, Federico Fagiani, Christian Rinaldi, Matteo Cantoni, Daniela Petti, Edoardo Albisetti, Marco Sampietro, Mariagrazia Ciardo, Giulia Siciliano, Pietro Alano, Brigitte Lemen, Joel B
    Advanced Science.2021;[Epub]     CrossRef
  • mHAT app for automated malaria rapid test result analysis and aggregation: a pilot study
    Carson Moore, Thomas Scherr, Japhet Matoba, Caison Sing’anga, Mukuma Lubinda, Phil Thuma, David Wright
    Malaria Journal.2021;[Epub]     CrossRef
  • Diagnostic Methods for Non-Falciparum Malaria
    Alba Marina Gimenez, Rodolfo F. Marques, Matías Regiart, Daniel Youssef Bargieri
    Frontiers in Cellular and Infection Microbiology.2021;[Epub]     CrossRef
  • Comparative Evaluation of Three Histidine-Rich Protein-2 Based Rapid Diagnostic Tests, Microscopy and PCR for Guiding Malaria Treatment in Ibadan, Southwest Nigeria
    AE Orimadegun, RI Funwei, OS Michael, OO Ogunkunle, JA Badejo, FI Olusola, O Agede, OE Anjorin, IO Ajayi, AS Jegede, O Ojurongbe, CO Falade
    Nigerian Journal of Clinical Practice.2021; 24(4): 496.     CrossRef
  • Development of Cooperative Primer-Based Real-Time PCR Assays for the Detection of Plasmodium malariae and Plasmodium ovale
    Felix Ansah, Jonathan Suurbaar, Derrick Darko, Nsoh G. Anabire, Samuel O. Blankson, Bright K.S. Domson, Alamissa Soulama, Paulina Kpasra, Jersley D. Chirawurah, Lucas Amenga-Etego, Prosper Kanyong, Gordon A. Awandare, Yaw Aniweh
    The Journal of Molecular Diagnostics.2021; 23(10): 1393.     CrossRef
  • Automated detection and staging of malaria parasites from cytological smears using convolutional neural networks
    Mira S. Davidson, Clare Andradi-Brown, Sabrina Yahiya, Jill Chmielewski, Aidan J. O’Donnell, Pratima Gurung, Myriam D. Jeninga, Parichat Prommana, Dean W. Andrew, Michaela Petter, Chairat Uthaipibull, Michelle J. Boyle, George W. Ashdown, Jeffrey D. Dvori
    Biological Imaging.2021;[Epub]     CrossRef
  • Ultraviolet/Visible and Near-Infrared Dual Spectroscopic Method for Detection and Quantification of Low-Level Malaria Parasitemia in Whole Blood
    John A. Adegoke, Amanda De Paoli, Isaac O. Afara, Kamila Kochan, Darren J. Creek, Philip Heraud, Bayden R. Wood
    Analytical Chemistry.2021; 93(39): 13302.     CrossRef
  • A Comparative Study of Diagnostic Methods of Malaria - Microscopy Versus Rapid Diagnostic Test Kits in a Tertiary Care Hospital, Rajasthan
    Saumya Singh, Neelam Chauhan, Jyoti Tomar, Aditya Pratap Singh
    Journal of Evidence Based Medicine and Healthcare.2021; 8(22): 1826.     CrossRef
  • Performance evaluation of RDT, light microscopy, and PET-PCR for detecting Plasmodium falciparum malaria infections in the 2018 Zambia National Malaria Indicator Survey
    Mulenga C. Mwenda, Abebe A. Fola, Ilinca I. Ciubotariu, Conceptor Mulube, Brenda Mambwe, Rachael Kasaro, Moonga B. Hawela, Busiku Hamainza, John M. Miller, Giovanna Carpi, Daniel J. Bridges
    Malaria Journal.2021;[Epub]     CrossRef
  • Application of dried blood spot sample pooling strategies for Plasmodium 18S rRNA biomarker testing to facilitate identification of infected persons in large-scale epidemiological studies
    Ming Chang, Selena Johnston, Annette M. Seilie, Dianna Hergott, Sean C. Murphy
    Malaria Journal.2021;[Epub]     CrossRef
  • Molecular characterization of sulphadoxine-pyrimethamine resistant malaria parasites among pregnant women in Anambra State, Nigeria
    Okezie Godwin Isaac, Mercy Ekejindu Ifeoma, Uchenna Eleje George, Chibuzo Ibeh Christian, Amauche Ezeagwuna Dorothy, Geoffrey Okafor Chigozie, Iherue Osuji Ahaneku
    Journal of Public Health and Epidemiology.2021; 13(4): 244.     CrossRef
  • Diagnosing Malaria Patients with Plasmodium falciparum and vivax Using Deep Learning for Thick Smear Images
    Yasmin M. Kassim, Feng Yang, Hang Yu, Richard J. Maude, Stefan Jaeger
    Diagnostics.2021; 11(11): 1994.     CrossRef
  • The Future in Sensing Technologies for Malaria Surveillance: A Review of Hemozoin-Based Diagnosis
    Vitória Baptista, Mariana S. Costa, Carla Calçada, Miguel Silva, José Pedro Gil, Maria Isabel Veiga, Susana O. Catarino
    ACS Sensors.2021; 6(11): 3898.     CrossRef
  • The Comparison of Real-time-PCR-HRM and Microscopy Methods for Detection of Mixed Plasmodium spp. Infections in Laghman Province, Afghanistan
    Abdolhossein Dalimi, Sayed Hussain Mosawi
    Infectious Disorders - Drug Targets .2021; 21(3): 399.     CrossRef
  • Review of the Current Landscape of the Potential of Nanotechnology for Future Malaria Diagnosis, Treatment, and Vaccination Strategies
    Arnau Guasch-Girbau, Xavier Fernàndez-Busquets
    Pharmaceutics.2021; 13(12): 2189.     CrossRef
  • A geostatistical framework for combining spatially referenced disease prevalence data from multiple diagnostics
    Benjamin Amoah, Peter J. Diggle, Emanuele Giorgi
    Biometrics.2020; 76(1): 158.     CrossRef
  • Diagnosis of Malaria Parasites Plasmodium spp. in Endemic Areas: Current Strategies for an Ancient Disease
    Brian Gitta, Nicole Kilian
    BioEssays.2020;[Epub]     CrossRef
  • Improving Accuracy of Malaria Diagnosis in Underserved Rural and Remote Endemic Areas of Sub-Saharan Africa: A Call to Develop Multiplexing Rapid Diagnostic Tests
    Rasheed O. Makanjuola, Andrew W. Taylor-Robinson
    Scientifica.2020; 2020: 1.     CrossRef
  • Assessment of Expert-Level Automated Detection of Plasmodium falciparum in Digitized Thin Blood Smear Images
    Po-Chen Kuo, Hao-Yuan Cheng, Pi-Fang Chen, Yu-Lun Liu, Martin Kang, Min-Chu Kuo, Shih-Fen Hsu, Hsin-Jung Lu, Stefan Hong, Chan-Hung Su, Ding-Ping Liu, Yi-Chin Tu, Jen-Hsiang Chuang
    JAMA Network Open.2020; 3(2): e200206.     CrossRef
  • Stringent Selection of Knobby Plasmodium falciparum-Infected Erythrocytes during Cytoadhesion at Febrile Temperature
    Michael Dörpinghaus, Finn Fürstenwerth, Lisa K. Roth, Philip Bouws, Maximilian Rakotonirinalalao, Vincent Jordan, Michaela Sauer, Torben Rehn, Eva Pansegrau, Katharina Höhn, Paolo Mesén-Ramírez, Anna Bachmann, Stephan Lorenzen, Thomas Roeder, Nahla Galal
    Microorganisms.2020; 8(2): 174.     CrossRef
  • Detection of Rare Objects by Flow Cytometry: Imaging, Cell Sorting, and Deep Learning Approaches
    Denis V. Voronin, Anastasiia A. Kozlova, Roman A. Verkhovskii, Alexey V. Ermakov, Mikhail A. Makarkin, Olga A. Inozemtseva, Daniil N. Bratashov
    International Journal of Molecular Sciences.2020; 21(7): 2323.     CrossRef
  • Comparision of the various routine diagnostic modalities of malaria and a new method: the Parasight™ platform
    Sindhusuta Das, Nonika Rajkumari, U. Revathi, Anusha Gururajan
    Journal of Parasitic Diseases.2020; 44(3): 528.     CrossRef
  • Severe malaria. Current concepts and practical overview: What every intensivist should know
    Mervyn Mer, Martin W. Dünser, Regina Giera, Arjen M. Dondorp
    Intensive Care Medicine.2020; 46(5): 907.     CrossRef
  • Plasmodium falciparum Histidine-Rich Protein 2 and 3 Gene Deletions and Their Implications in Malaria Control
    Josphat Nyataya, John Waitumbi, Victor A. Mobegi, Ayman Noreddin, Mohamed E. El Zowalaty
    Diseases.2020; 8(2): 15.     CrossRef
  • Targeted repression of Plasmodium apicortin by host microRNA impairs malaria parasite growth and invasion
    Malabika Chakrabarti, Swati Garg, Ayana Rajagopal, Soumya Pati, Shailja Singh
    Disease Models & Mechanisms.2020;[Epub]     CrossRef
  • A Deep Learning Approach for Segmentation of Red Blood Cell Images and Malaria Detection
    Maria Delgado-Ortet, Angel Molina, Santiago Alférez, José Rodellar, Anna Merino
    Entropy.2020; 22(6): 657.     CrossRef
  • Spatial and epidemiological drivers of Plasmodium falciparum malaria among adults in the Democratic Republic of the Congo
    Molly Deutsch-Feldman, Nicholas F Brazeau, Jonathan B Parr, Kyaw L Thwai, Jeremie Muwonga, Melchior Kashamuka, Antoinette Tshefu Kitoto, Ozkan Aydemir, Jeffrey A Bailey, Jessie K Edwards, Robert Verity, Michael Emch, Emily W Gower, Jonathan J Juliano, Ste
    BMJ Global Health.2020; 5(6): e002316.     CrossRef
  • Evaluating interventions to improve test, treat, and track (T3) malaria strategy among over-the-counter medicine sellers (OTCMS) in some rural communities of Fanteakwa North district, Ghana: study protocol for a cluster randomized controlled trial
    Olajoju Temidayo Soniran, Benjamin Abuaku, Collins Stephen Ahorlu
    Trials.2020;[Epub]     CrossRef
  • Design, synthesis and biological evaluation of several aromatic substituted chalcones as antimalarial agents
    Adarsh Gopinathan, Mahreen Moidu, Minil Mukundan, Siju Ellickal Narayanan, Hariraj Narayanan, Navin Adhikari
    Drug Development Research.2020; 81(8): 1048.     CrossRef
  • Utility of Rapid Diagnostic Tests for Detection of Malarial Antigens and Their Comparison with Peripheral Blood Smear Examination
    Shreshy Singh, Sangeeta Dey Akoljam, Dhananjay Kumar, Aninda Sen, Ashit Kumar
    Journal of Evolution of Medical and Dental Sciences.2020; 9(15): 1291.     CrossRef
  • Detection and stage classification of Plasmodium falciparum from images of Giemsa stained thin blood films using random forest classifiers
    Syed Saiden Abbas, Tjeerd M. H. Dijkstra
    Diagnostic Pathology.2020;[Epub]     CrossRef
  • ITEM-THREE analysis of a monoclonal anti-malaria antibody reveals its assembled epitope on the pfMSP119 antigen
    Kwabena F.M. Opuni, Cornelia Koy, Manuela Russ, Maren Reepmeyer, Bright D. Danquah, Moritz Weresow, Astrid Alef, Peter Lorenz, Hans-Juergen Thiesen, Michael O. Glocker
    Journal of Biological Chemistry.2020; 295(44): 14987.     CrossRef
  • Malaria distribution and performance of malaria diagnostic methods in Malaysia (1980–2019): a systematic review
    Mohd Amirul Fitri A. Rahim, Mohd Bakhtiar Munajat, Zulkarnain Md Idris
    Malaria Journal.2020;[Epub]     CrossRef
  • Inter-rater Variability in Malaria Microscopy at the LEKMA Hospital, Ghana
    Andrew Nii Adzei Bekoe, Emmanuel Alote Allotey, Elliot Elikplim Akorsu, Albert Abaka-Yawson, Samuel Adusei, Godsway Edem Kpene, Precious Kwablah Kwadzokpui, Lizandra Guidi Magalhães
    Journal of Parasitology Research.2020; 2020: 1.     CrossRef
  • STUDY OF THREE MALARIA RAPID DETECTION TESTS AND ITS CORRELATION WITH PARASITIC INDEX FOR P.FALCIPARUM AND P.VIVAX
    Dipti Gaikwad, Chaya A. Kumar, Sujata Baveja
    INDIAN JOURNAL OF APPLIED RESEARCH.2020; : 26.     CrossRef
  • Fever and Serology

    Pediatric Infectious Disease.2020; 2(1): 29.     CrossRef
  • Diagnostic Value of Plasmotec Malaria-3 Antigen Detection on Gold Standard Microscopy
    Trieva Verawaty Butarbutar, Puspa Wardhani, Aryati Aryati
    INDONESIAN JOURNAL OF CLINICAL PATHOLOGY AND MEDICAL LABORATORY.2020; 26(2): 210.     CrossRef
  • Rapid diagnosis of parasitic diseases: current scenario and future needs
    S. Momčilović, C. Cantacessi, V. Arsić-Arsenijević, D. Otranto, S. Tasić-Otašević
    Clinical Microbiology and Infection.2019; 25(3): 290.     CrossRef
  • Development of an aptamer-based field effect transistor biosensor for quantitative detection of Plasmodium falciparum glutamate dehydrogenase in serum samples
    Naveen K. Singh, Phurpa Dema Thungon, Pedro Estrela, Pranab Goswami
    Biosensors and Bioelectronics.2019; 123: 30.     CrossRef
  • Paper Microfluidics for Point-of-Care Blood-Based Analysis and Diagnostics
    Hua Li, Andrew J. Steckl
    Analytical Chemistry.2019; 91(1): 352.     CrossRef
  • Plasmodium genomics: an approach for learning about and ending human malaria
    José Antonio Garrido-Cardenas, Lilia González-Cerón, Francisco Manzano-Agugliaro, Concepción Mesa-Valle
    Parasitology Research.2019; 118(1): 1.     CrossRef
  • Selecting better diagnostic kits for diagnosis of malarial parasites at point of care
    Prudhvi Chand Mallepaddi, Soumendra Nath Maity, Revathi Poonati, Nagababu Pyadala, Rathnagiri Polavarapu, Usha Kiranmayi Mangamuri, Sudhakar Poda
    3 Biotech.2019;[Epub]     CrossRef
  • A 4-Day Incubation Period of Plasmodium falciparum Infection in a Nonimmune Patient in Ghana: A Case Report
    Verner Orish, Leslie Afutu, Oladapo Ayodele, Lorena Likaj, Aleksandra Marinkovic, Adekunle Sanyaolu
    Open Forum Infectious Diseases.2019;[Epub]     CrossRef
  • Enhancing the sensitivity of micro magnetic resonance relaxometry detection of low parasitemia Plasmodium falciparum in human blood
    Smitha Surendran Thamarath, Aoli Xiong, Po-Han Lin, Peter Rainer Preiser, Jongyoon Han
    Scientific Reports.2019;[Epub]     CrossRef
  • Health Information Literacy among Malaria Patients in Ghana: Sustainable Development Goals (SDG) 3 in Focus
    Dominic Agyei Dankwah, George Clifford Yamson
    The Open Public Health Journal.2019; 12(1): 100.     CrossRef
  • Bayesian evaluation of the performance of three diagnostic tests for Plasmodium falciparum infection in a low-transmission setting in Kilifi County, Kenya
    Marshal M. Mweu, Juliana Wambua, Fixtan Njuga, Philip Bejon, Daniel Mwanga
    Wellcome Open Research.2019; 4: 67.     CrossRef
  • Molecular surveillance of pfhrp2 and pfhrp3 genes deletion in Plasmodium falciparum isolates and the implications for rapid diagnostic tests in Nigeria
    Roland Funwei, David Nderu, Christian N. Nguetse, Bolaji N. Thomas, Catherine O. Falade, Thirumalaisamy P Velavan, Olusola Ojurongbe
    Acta Tropica.2019; 196: 121.     CrossRef
  • Bayesian evaluation of the performance of three diagnostic tests for Plasmodium falciparum infection in a low-transmission setting in Kilifi County, Kenya
    Marshal M. Mweu, Juliana Wambua, Fixtan Njuga, Philip Bejon, Daniel Mwanga
    Wellcome Open Research.2019; 4: 67.     CrossRef
  • Knowledge, Attitude, and Practice Related to Malaria Diagnosis among Healthcare Workers in Hospitals: A Cross-Sectional Survey
    Kwuntida Uthaisar Kotepui, Manas Kotepui, Chuchard Punsawad
    Journal of Tropical Medicine.2019; 2019: 1.     CrossRef
  • Persistence of Imported Malaria Into the United Kingdom: An Epidemiological Review of Risk Factors and At-risk Groups
    Qubekani M Moyo, Martin Besser, Roderick Lynn, Andrew M L Lever
    Clinical Infectious Diseases.2019; 69(7): 1156.     CrossRef
  • Malaria: The Past and the Present
    Jasminka Talapko, Ivana Škrlec, Tamara Alebić, Melita Jukić, Aleksandar Včev
    Microorganisms.2019; 7(6): 179.     CrossRef
  • Differences in infection patterns of vector-borne blood-stage parasites of sympatric Malagasy primate species (Microcebus murinus, M. ravelobensis)
    Annette Klein, Christina Strube, Ute Radespiel, Andrea Springer, Elke Zimmermann
    International Journal for Parasitology: Parasites and Wildlife.2019; 10: 59.     CrossRef
  • Malaria-Infected Red Blood Cell Analysis through Optical and Biochemical Parameters Using the Transport of Intensity Equation and the Microscope’s Optical Properties
    Marcel Agnero, Kouakou Konan, Zan Tokou, Yao Kossonou, Bienvenue Dion, Kenneth Kaduki, Jérémie Zoueu
    Sensors.2019; 19(14): 3045.     CrossRef
  • Digital PCR: a new technology for diagnosis of parasitic infections
    E. Pomari, C. Piubelli, F. Perandin, Z. Bisoffi
    Clinical Microbiology and Infection.2019; 25(12): 1510.     CrossRef
  • Bayesian evaluation of the performance of three diagnostic tests for Plasmodium falciparum infection in a low-transmission setting in Kilifi County, Kenya
    Marshal M. Mweu, Juliana Wambua, Fixtan Njuga, Philip Bejon, Daniel Mwanga
    Wellcome Open Research.2019; 4: 67.     CrossRef
  • Evaluación de la calidad del diagnóstico de malaria en la red local de laboratorios y en los laboratorios intermedios en el contexto de la eliminación de la enfermedad en Ecuador
    Nohora Marcela Mendoza, César Eduardo Díaz, Yim Yan Wong, Adriana Estefanía Echeverría, Doris Grimaneza Guale, Rosa Haydeé Delgado, José Mauricio Muñoz, Luis Fernando Solórzano, Marcelo Eduardo Andrade, Rosa Alba Quintero, Belinda Regina Palacios, Saida M
    Biomédica.2019; 39(Supl. 2): 101.     CrossRef
  • Diagnostic performance of CareStart™ malaria HRP2/pLDH test in comparison with standard microscopy for detection of uncomplicated malaria infection among symptomatic patients, Eastern Coast of Tanzania
    George M. Bwire, Billy Ngasala, Manase Kilonzi, Wigilya P. Mikomangwa, Fatuma F. Felician, Appolinary A. R. Kamuhabwa
    Malaria Journal.2019;[Epub]     CrossRef
  • Occurrence and seasonal variation of human Plasmodium infection in Punjab Province, Pakistan
    Naveeda Akhtar Qureshi, Huma Fatima, Muhammad Afzal, Aamir Ali Khattak, Muhammad Ali Nawaz
    BMC Infectious Diseases.2019;[Epub]     CrossRef
  • Diagnostic tools used in the evaluation of acute febrile illness in South India: a scoping review
    Divyalakshmi Bhaskaran, Sarabjit Singh Chadha, Sanjay Sarin, Rajashree Sen, Sonia Arafah, Sabine Dittrich
    BMC Infectious Diseases.2019;[Epub]     CrossRef
  • Characterizing the Spatial Determinants and Prevention of Malaria in Kenya
    Sucharita Gopal, Yaxiong Ma, Chen Xin, Joshua Pitts, Lawrence Were
    International Journal of Environmental Research and Public Health.2019; 16(24): 5078.     CrossRef
  • Cost-effectiveness analysis of malaria rapid diagnostic tests: a systematic review
    Xiao-Xiao Ling, Jia-Jie Jin, Guo-Ding Zhu, Wei-Ming Wang, Yuan-Yuan Cao, Meng-Meng Yang, Hua-Yun Zhou, Jun Cao, Jia-Yan Huang
    Infectious Diseases of Poverty.2019;[Epub]     CrossRef
  • EFFECT OF ARTIFICIAL INTELLIGENCE-BASED TECHNOLOGY IN MALARIA DIAGNOSIS
    Gorav Kumar, Prabhash Bhavsar
    Journal of Evidence Based Medicine and Healthcare.2019; 6(29): 1923.     CrossRef
  • Identification of Highly Expressed Plasmodium Vivax Proteins from Clinical Isolates Using Proteomics
    Apoorva Venkatesh, Anwesha Lahiri, Panga Jaipal Reddy, Jayanthi Shastri, Sheetal Bankar, Swati Patankar, Sanjeeva Srivastava
    PROTEOMICS – Clinical Applications.2018;[Epub]     CrossRef
  • Evaluation of fluorescent in-situ hybridization technique for diagnosis of malaria in Ahero Sub-County hospital, Kenya
    Regina Kandie, Rachel Ochola, Kariuki Njaanake
    BMC Infectious Diseases.2018;[Epub]     CrossRef
  • Malaria in India: The Need for New Targets for Diagnosis and Detection of Plasmodium vivax
    Swati Patankar, Shobhona Sharma, Pradipsinh K. Rathod, Manoj T. Duraisingh
    PROTEOMICS – Clinical Applications.2018;[Epub]     CrossRef
  • Fabrication of a Lab-on-Chip Device Using Material Extrusion (3D Printing) and Demonstration via Malaria-Ab ELISA
    Maria Bauer, Lawrence Kulinsky
    Micromachines.2018; 9(1): 27.     CrossRef
  • Image analysis and machine learning for detecting malaria
    Mahdieh Poostchi, Kamolrat Silamut, Richard J. Maude, Stefan Jaeger, George Thoma
    Translational Research.2018; 194: 36.     CrossRef
  • Diagnostic tools in childhood malaria
    Amirah Amir, Fei-Wen Cheong, Jeremy R. De Silva, Yee-Ling Lau
    Parasites & Vectors.2018;[Epub]     CrossRef
  • Malaria Disease Recommendations for Solid Organ Transplant Recipients and Donors
    Lígia Camera Pierrotti, Marilyn Eckstein Levi, Silvia Maria Di Santi, Aluísio Cotrim Segurado, Eskild Petersen
    Transplantation.2018; 102(2S): S16.     CrossRef
  • Converging Human and Malaria Vector Diagnostics with Data Management towards an Integrated Holistic One Health Approach
    Konstantinos Mitsakakis, Sebastian Hin, Pie Müller, Nadja Wipf, Edward Thomsen, Michael Coleman, Roland Zengerle, John Vontas, Konstantinos Mavridis
    International Journal of Environmental Research and Public Health.2018; 15(2): 259.     CrossRef
  • Malaria diagnosis by PCR revealed differential distribution of mono and mixed species infections by Plasmodium falciparum and P. vivax in India
    Nisha Siwal, Upasana Shyamsunder Singh, Manoswini Dash, Sonalika Kar, Swati Rani, Charu Rawal, Rajkumar Singh, Anupkumar R. Anvikar, Veena Pande, Aparup Das, Georges Snounou
    PLOS ONE.2018; 13(3): e0193046.     CrossRef
  • Development of a high-throughput flexible quantitative suspension array assay for IgG against multiple Plasmodium falciparum antigens
    Itziar Ubillos, Joseph J. Campo, Alfons Jiménez, Carlota Dobaño
    Malaria Journal.2018;[Epub]     CrossRef
  • Capacitive malaria aptasensor using Plasmodium falciparum glutamate dehydrogenase as target antigen in undiluted human serum
    Naveen K. Singh, Sunil K. Arya, Pedro Estrela, Pranab Goswami
    Biosensors and Bioelectronics.2018; 117: 246.     CrossRef
  • Seasonal variations in Plasmodium falciparum parasite prevalence assessed by varying diagnostic tests in asymptomatic children in southern Ghana
    Ruth Ayanful-Torgby, Neils B. Quashie, Johnson N. Boampong, Kim C. Williamson, Linda E. Amoah, Luzia Helena Carvalho
    PLOS ONE.2018; 13(6): e0199172.     CrossRef
  • Epidemiology of Malaria in Yulin, South China 1999–2016: Imported Malaria Threatens Zero Local Case Status
    Yan Yang, Yiwei Liu, Zhichun Xie, Shuzhi Wu, Lu Yang, Wen Li, Xinbin Quan
    Vector-Borne and Zoonotic Diseases.2018; 18(10): 533.     CrossRef
  • A portable, optical scanning microsystem for large field of view, high resolution imaging of biological specimens
    Georgia Korompili, Georgios Kanakaris, Christos Ampatis, Nikos Chronis
    Sensors and Actuators A: Physical.2018; 279: 367.     CrossRef
  • Malaria and the ‘last’ parasite: how can technology help?
    Ngoc Minh Pham, Walter Karlen, Hans-Peter Beck, Emmanuel Delamarche
    Malaria Journal.2018;[Epub]     CrossRef
  • A diagnostic performance evaluation of rapid diagnostic tests and microscopy for malaria diagnosis using nested polymerase chain reaction as reference standard in a tertiary hospital in Jos, Nigeria
    Okokon I Ita, Akaninyene A Otu, Kenneth Onyedibe, Anthony A Iwuafor, Edmund Banwat, Daniel Z Egah
    Transactions of The Royal Society of Tropical Medicine and Hygiene.2018; 112(10): 436.     CrossRef
  • Serological and molecular techniques applied for identification of Plasmodium spp. in blood samples from nonhuman primates
    Mayra Araguaia Pereira Figueiredo, Silvia Maria Di Santi, Wilson Gómez Manrique, Marcos Rogério André, Rosangela Zacarias Machado
    Revista Brasileira de Parasitologia Veterinária.2018;[Epub]     CrossRef
  • Assessing the performance of only HRP2 and HRP2 with pLDH based rapid diagnostic tests for the diagnosis of malaria in middle Ghana, Africa
    Dennis Adu-Gyasi, Kwaku Poku Asante, Sabastina Amoako, Nicholas Amoako, Love Ankrah, David Dosoo, Samuel Kofi Tchum, George Adjei, Oscar Agyei, Seeba Amenga-Etego, Seth Owusu-Agyei, Henk D. F. H. Schallig
    PLOS ONE.2018; 13(9): e0203524.     CrossRef
  • Microscopic malaria parasitemia diagnosis and grading on benchmark datasets
    Amjad Rehman, Naveed Abbas, Tanzila Saba, Zahid Mehmood, Toqeer Mahmood, Khawaja Tehseen Ahmed
    Microscopy Research and Technique.2018; 81(9): 1042.     CrossRef
  • Diurnal variation in expired breath volatiles in malaria-infected and healthy volunteers
    Amalia Z Berna, James S McCarthy, X Rosalind Wang, Michelle Michie, Florence G Bravo, Julie Cassells, Stephen C Trowell
    Journal of Breath Research.2018; 12(4): 046014.     CrossRef
  • Diagnostic tools for tackling febrile illness and enhancing patient management
    Konstantinos Mitsakakis, Valérie D'Acremont, Sebastian Hin, Felix von Stetten, Roland Zengerle
    Microelectronic Engineering.2018; 201: 26.     CrossRef
  • Deep convolution neural network for image recognition
    Boukaye Boubacar Traore, Bernard Kamsu-Foguem, Fana Tangara
    Ecological Informatics.2018; 48: 257.     CrossRef
  • A case of importedPlasmodium Falciparumchloroquine and Sulfadoxine-Pyrimethamine sensitive in a Finland male presentation
    N P D Witari, S Masyeni, N W Rusni, K T Sumadewi, A E Pratiwi, P B Asih
    IOP Conference Series: Materials Science and Engineering.2018; 434: 012145.     CrossRef
  • Accuracy of One Step malaria rapid diagnostic test (RDT) in detecting Plasmodium falciparum placental malaria infection in women living in Yaoundé, Cameroon
    Rosette Megnekou, Jean Claude Djontu, Benderli C. Nana, Jude D. Bigoga, Maurice Fotso, Balotin Fogang, Rose F. G. Leke
    Malaria Journal.2018;[Epub]     CrossRef
  • Clinical and laboratory features associated with acute kidney injury in severe malaria
    Sandeep Mahajan, Prayas Sethi, Hiren Anghan, Manish Soneja, Naveet Wig
    Indian Journal of Critical Care Medicine.2018; 22(10): 718.     CrossRef
  • Computational study of a magnetic design to improve the diagnosis of malaria: 2D model
    Siddharth Vyas, Vladimir Genis, Gary Friedman
    Journal of Magnetism and Magnetic Materials.2017; 423: 301.     CrossRef
  • Aptamer Technology: Adjunct Therapy for Malaria
    Nik Nik Kamarudin, Nurul Mohammed, Khairul Mustaffa
    Biomedicines.2017; 5(1): 1.     CrossRef
  • Performance of loop-mediated isothermal amplification (LAMP) for the diagnosis of malaria among malaria suspected pregnant women in Northwest Ethiopia
    Banchamlak Tegegne, Sisay Getie, Wossenseged Lemma, Abu Naser Mohon, Dylan R. Pillai
    Malaria Journal.2017;[Epub]     CrossRef
  • New potential Plasmodium brasilianum hosts: tamarin and marmoset monkeys (family Callitrichidae)
    Denise A. M. Alvarenga, Anielle Pina-Costa, Cesare Bianco, Silvia B. Moreira, Patricia Brasil, Alcides Pissinatti, Claudio T. Daniel-Ribeiro, Cristiana F. A. Brito
    Malaria Journal.2017;[Epub]     CrossRef
  • Malaria in British military personnel deployed to Sierra Leone: a case series
    Oliver Quantick, R Howlett-Shipley, S Roughton, D Ross
    Journal of the Royal Army Medical Corps.2017; 163(1): 65.     CrossRef
  • Erythrocyte segmentation for quantification in microscopic images of thin blood smears
    Salam Shuleenda Devi, Joyeeta Singha, Manish Sharma, Rabul Hussain Laskar
    Journal of Intelligent & Fuzzy Systems.2017; 32(4): 2847.     CrossRef
  • A portable image-based cytometer for rapid malaria detection and quantification
    Dahou Yang, Gowtham Subramanian, Jinming Duan, Shaobing Gao, Li Bai, Rajesh Chandramohanadas, Ye Ai, Georges Snounou
    PLOS ONE.2017; 12(6): e0179161.     CrossRef
  • A Simple, Efficient and Ultrasensitive Gold Nanourchin Based Electrochemical Sensor for the Determination of an Antimalarial Drug: Mefloquine
    Tirivashe Elton Chiwunze, Neeta Bachheti Thapliyal, Venkata Narayana Palakollu, Rajshekhar Karpoormath
    Electroanalysis.2017; 29(9): 2138.     CrossRef
  • Development of an Immunosensor for PfHRP 2 as a Biomarker for Malaria Detection
    Aver Hemben, Jon Ashley, Ibtisam Tothill
    Biosensors.2017; 7(3): 28.     CrossRef
  • Quantitation of Malarial parasitemia in Giemsa stained thin blood smears using Six Sigma threshold as preprocessor
    Srinivasan Sankaran, Muthukumaran Malarvel, Gopalakrishnan Sethumadhavan, Dinkar Sahal
    Optik.2017; 145: 225.     CrossRef
  • State of diagnosing infectious pathogens using colloidal nanomaterials
    Jisung Kim, Mohamed A. Abdou Mohamed, Kyryl Zagorovsky, Warren C.W. Chan
    Biomaterials.2017; 146: 97.     CrossRef
  • Single Domain Antibodies as New Biomarker Detectors
    Chiuan Leow, Katja Fischer, Chiuan Leow, Qin Cheng, Candy Chuah, James McCarthy
    Diagnostics.2017; 7(4): 52.     CrossRef
  • Detection of Plasmodium falciparum DNA in saliva samples stored at room temperature: potential for a non-invasive saliva-based diagnostic test for malaria
    Kenji O. Mfuh, Samuel Tassi Yunga, Livo F. Esemu, Obase Ngemani Bekindaka, Jessica Yonga, Jean Claude Djontu, Calixt D. Mbakop, Diane W. Taylor, Vivek R. Nerurkar, Rose G. F. Leke
    Malaria Journal.2017;[Epub]     CrossRef
  • Diagnostic accuracy of rapid antigen test for malaria and determinants of heavy malaria parasitaemia in children at the Nnamdi Azikiwe University Teaching Hospital, Nnewi, Nigeria
    EI Nwaneli, CD I Osuorah, JC Ebenebe, N Umeadi
    Nigerian Journal of Health Sciences.2017; 17(2): 59.     CrossRef
  • A STUDY OF PAPAYA EXTRACT IN THE TREATMENT OF LOW PLATELET COUNT IN MALARIA AND DENGUE CHILDREN BELOW 18 YEARS
    Gopi Mohan R
    Journal of Evidence Based Medicine and Healthcare.2017; 4(21): 1193.     CrossRef
  • Comparative Assessment of Private and Public Health Care Providers' Knowledge on Malaria Treatment in Bassa Local Government Area of Plateau State
    Nanloh Samuel Jimam, Shalkur David, Bulus J. Kaben
    Current Medical Issues.2017; 15(1): 45.     CrossRef
  • Small angle light scattering assay for the detection of malaria infection
    R.A. Inocêncio da Luz, H.M. Mavoko, I. Crandall, S. Deshpande, P. Lutumba, J.P. Van geertruyden
    Talanta.2016; 147: 473.     CrossRef
  • Comparison of Partec Rapid Malaria Test with Conventional Light Microscopy for Diagnosis of Malaria in Northwest Ethiopia
    Meseret Birhanie
    Journal of Parasitology Research.2016; 2016: 1.     CrossRef
  • Deformability based sorting of red blood cells improves diagnostic sensitivity for malaria caused by Plasmodium falciparum
    Quan Guo, Simon P. Duffy, Kerryn Matthews, Xiaoyan Deng, Aline T. Santoso, Emel Islamzada, Hongshen Ma
    Lab Chip.2016; 16(4): 645.     CrossRef
  • Two-stage sample-to-answer system based on nucleic acid amplification approach for detection of malaria parasites
    Qing Liu, Jeonghun Nam, Sangho Kim, Chwee Teck Lim, Mi Kyoung Park, Yong Shin
    Biosensors and Bioelectronics.2016; 82: 1.     CrossRef
  • Review of Surface Enhanced Raman Spectroscopy for Malaria Diagnosis and a New Approach for the Detection of Single Parasites in the Ring Stage
    Keren Chen, Clint Perlaki, Aoli Xiong, Peter Preiser, Quan Liu
    IEEE Journal of Selected Topics in Quantum Electronics.2016; 22(4): 179.     CrossRef
  • High resolution FTIR imaging provides automated discrimination and detection of single malaria parasite infected erythrocytes on glass
    David Perez-Guaita, Dean Andrew, Philip Heraud, James Beeson, David Anderson, Jack Richards, Bayden R. Wood
    Faraday Discussions.2016; 187: 341.     CrossRef
  • Hemoglobin consumption by P. falciparum in individual erythrocytes imaged via quantitative phase spectroscopy
    Matthew T. Rinehart, Han Sang Park, Katelyn A. Walzer, Jen-Tsan Ashley Chi, Adam Wax
    Scientific Reports.2016;[Epub]     CrossRef
  • Continuous-Flow Separation of Malaria-Infected Human Erythrocytes Using DC Dielectrophoresis: An Electrokinetic Modeling and Simulation
    Milad Nahavandi
    Industrial & Engineering Chemistry Research.2016; 55(19): 5484.     CrossRef
  • Nerolidol: A Sesquiterpene Alcohol with Multi-Faceted Pharmacological and Biological Activities
    Weng-Keong Chan, Loh Tan, Kok-Gan Chan, Learn-Han Lee, Bey-Hing Goh
    Molecules.2016; 21(5): 529.     CrossRef
  • High-throughput malaria parasite separation using a viscoelastic fluid for ultrasensitive PCR detection
    Jeonghun Nam, Yong Shin, Justin Kok Soon Tan, Ying Bena Lim, Chwee Teck Lim, Sangho Kim
    Lab on a Chip.2016; 16(11): 2086.     CrossRef
  • Research progress in electroanalytical techniques for determination of antimalarial drugs in pharmaceutical and biological samples
    Neeta Thapliyal, Tirivashe E. Chiwunze, Rajshekhar Karpoormath, Rajendra N. Goyal, Harun Patel, Srinivasulu Cherukupalli
    RSC Advances.2016; 6(62): 57580.     CrossRef
  • Clinical malaria diagnosis: rule-based classification statistical prototype
    Francis Bbosa, Ronald Wesonga, Peter Jehopio
    SpringerPlus.2016;[Epub]     CrossRef
  • The development of malaria diagnostic techniques: a review of the approaches with focus on dielectrophoretic and magnetophoretic methods
    Surasak Kasetsirikul, Jirayut Buranapong, Werayut Srituravanich, Morakot Kaewthamasorn, Alongkorn Pimpin
    Malaria Journal.2016;[Epub]     CrossRef
  • Delayed Diagnosis of Falciparum Malaria with Acute Kidney Injury
    Iee Ho Choi, Pyoung Han Hwang, Sam Im Choi, Dae-Yeol Lee, Min Sun Kim
    Journal of Korean Medical Science.2016; 31(9): 1499.     CrossRef
  • Utility of nested polymerase chain reaction over the microscopy and immuno-chromatographic test in the detection of Plasmodium species and their clinical spectrum
    P. Ranjan, U. Ghoshal
    Parasitology Research.2016; 115(9): 3375.     CrossRef
  • Minimising invasiveness in diagnostics: developing a rapid urine‐based monoclonal antibody dipstick test for malaria
    Uri S. Markakpo, Kwabena M. Bosompem, Mawuli Dzodzomenyo, Anthony Danso‐Appiah, Edward E. Essuman, William K. Anyan, Mitsuko Suzuki, Judith K. Stephens, Isaac Anim‐Baidoo, Richard H. Asmah, Michael F. Ofori, Parnor Madjitey, Jonas B. Danquah, Naa Adjeley
    Tropical Medicine & International Health.2016; 21(10): 1263.     CrossRef
  • Field evaluation of diagnostic performance of malaria rapid diagnostic tests in western Kenya
    Elizabeth W. Wanja, Nickline Kuya, Collins Moranga, Mark Hickman, Jacob D. Johnson, Carolyne Moseti, Lalaine Anova, Bernhards Ogutu, Colin Ohrt
    Malaria Journal.2016;[Epub]     CrossRef
  • SPECT/CT analysis of splenic function in genistein-treated malaria-infected mice
    Young Ran Ha, Sung-A. Kang, Jeongeun Ryu, Eunseop Yeom, Mun Ki Kim, Sang Joon Lee
    Experimental Parasitology.2016; 170: 10.     CrossRef
  • Comparative Performance Evaluation of Routine Malaria Diagnosis at Ho Municipal Hospital
    James Osei-Yeboah, Gameli Kwame Norgbe, Sylvester Yao Lokpo, Mohammed Khadijah Kinansua, Loverage Nettey, Emmanuel Alote Allotey
    Journal of Parasitology Research.2016; 2016: 1.     CrossRef
  • Working principle and application of magnetic separation for biomedical diagnostic at high- and low-field gradients
    Sim Siong Leong, Swee Pin Yeap, JitKang Lim
    Interface Focus.2016; 6(6): 20160048.     CrossRef
  • Serological markers to measure recent changes in malaria at population level in Cambodia
    Karen Kerkhof, Vincent Sluydts, Laura Willen, Saorin Kim, Lydie Canier, Somony Heng, Takafumi Tsuboi, Tho Sochantha, Siv Sovannaroth, Didier Ménard, Marc Coosemans, Lies Durnez
    Malaria Journal.2016;[Epub]     CrossRef
  • Colorimetric Detection of Plasmodium vivax in Urine Using MSP10 Oligonucleotides and Gold Nanoparticles
    Yossef Alnasser, Cusi Ferradas, Taryn Clark, Maritza Calderon, Alejandro Gurbillon, Dionicia Gamboa, Uri S. McKakpo, Isabella A. Quakyi, Kwabena M. Bosompem, David J. Sullivan, Joseph M. Vinetz, Robert H. Gilman, Eric Dumonteil
    PLOS Neglected Tropical Diseases.2016; 10(10): e0005029.     CrossRef
  • Cost Effectiveness of Giemsa versus Field’s Staining Technique: Implications for Malaria Diagnosis among Children in a Busy Hospital Setting in Uganda
    Juliana Namutundu, Nsobya Samuel Lubwama, Yeka Adoke, Chrispus Mayora, Sebastian Olikira Baine
    Nursing and Health Care.2016; : 26.     CrossRef
  • Parasites
    Elitza S. Theel, Bobbi S. Pritt, Randall T. Hayden, Donna M. Wolk, Karen C. Carroll, Yi-Wei Tang
    Microbiology Spectrum.2016;[Epub]     CrossRef
  • The utility of serial blood film testing for the diagnosis of malaria
    Karan S. Makhija, Samuel Maloney, Robert Norton
    Pathology.2015; 47(1): 68.     CrossRef
  • Dynamical footprint of falcipain-2 catalytic triad in hemoglobin-β-bound state
    I.O. Omotuyi, T. Hamada
    Journal of Biomolecular Structure and Dynamics.2015; 33(5): 1027.     CrossRef
  • Malaria detection using inertial microfluidics
    Majid Ebrahimi Warkiani, Andy Kah Ping Tay, Bee Luan Khoo, Xu Xiaofeng, Jongyoon Han, Chwee Teck Lim
    Lab on a Chip.2015; 15(4): 1101.     CrossRef
  • Digital image analysis for automatic enumeration of malaria parasites using morphological operations
    J.E. Arco, J.M. Górriz, J. Ramírez, I. Álvarez, C.G. Puntonet
    Expert Systems with Applications.2015; 42(6): 3041.     CrossRef
  • Computational microscopic imaging for malaria parasite detection: a systematic review
    D.K. DAS, R. MUKHERJEE, C. CHAKRABORTY
    Journal of Microscopy.2015; 260(1): 1.     CrossRef
  • Enhancing malaria diagnosis through microfluidic cell enrichment and magnetic resonance relaxometry detection
    Tian Fook Kong, Weijian Ye, Weng Kung Peng, Han Wei Hou, Marcos, Peter Rainer Preiser, Nam-Trung Nguyen, Jongyoon Han
    Scientific Reports.2015;[Epub]     CrossRef
  • Implementation and application of a multiplex assay to detect malaria-specific antibodies: a promising tool for assessing malaria transmission in Southeast Asian pre-elimination areas
    Karen Kerkhof, Lydie Canier, Saorin Kim, Somony Heng, Tho Sochantha, Siv Sovannaroth, Inès Vigan-Womas, Marc Coosemans, Vincent Sluydts, Didier Ménard, Lies Durnez
    Malaria Journal.2015;[Epub]     CrossRef
  • Novel techniques and future directions in molecular diagnosis of malaria in resource-limited settings
    Eniyou Cheryll Oriero, Jean-Pierre Van Geertruyden, Davis C Nwakanma, Umberto D’Alessandro, Jan Jacobs
    Expert Review of Molecular Diagnostics.2015; 15(11): 1419.     CrossRef
  • Insecticide resistance in malaria-transmitting mosquitoes in Zimbabwe: a review
    White Soko, Moses J. Chimbari, Samson Mukaratirwa
    Infectious Diseases of Poverty.2015;[Epub]     CrossRef
  • Reduced deformability of parasitized red blood cells as a biomarker for anti-malarial drug efficacy
    Xiaoyan Deng, Simon P. Duffy, Marie-Eve Myrand-Lapierre, Kerryn Matthews, Aline Teresa Santoso, Yi-Ling Du, Katherine S. Ryan, Hongshen Ma
    Malaria Journal.2015;[Epub]     CrossRef
  • Point-of-Care Diagnostics in Low Resource Settings: Present Status and Future Role of Microfluidics
    Shikha Sharma, Julia Zapatero-Rodríguez, Pedro Estrela, Richard O'Kennedy
    Biosensors.2015; 5(3): 577.     CrossRef
  • Development of inexpensive blood imaging systems: where are we now?
    Kaiqin Chu, Zachary J Smith, Sebastian Wachsmann-Hogiu
    Expert Review of Medical Devices.2015; 12(5): 613.     CrossRef
  • Refined Method for Droplet Microfluidics-Enabled Detection of Plasmodium falciparum Encoded Topoisomerase I in Blood from Malaria Patients
    Marianne Hede, Patricia Okorie, Signe Fruekilde, Søren Fjelstrup, Jonas Thomsen, Oskar Franch, Cinzia Tesauro, Magnus Bugge, Mette Christiansen, Stéphane Picot, Felix Lötsch, Ghyslain Mombo-Ngoma, Johannes Mischlinger, Ayôla Adegnika, Finn Pedersen, Yi-Pi
    Micromachines.2015; 6(10): 1505.     CrossRef
  • Fluorescence In Situ Hybridization (FISH) Assays for Diagnosing Malaria in Endemic Areas
    Jyotsna Shah, Olivia Mark, Helena Weltman, Nicolas Barcelo, Wai Lo, Danuta Wronska, Srinivas Kakkilaya, Aravinda Rao, Shalia T. Bhat, Ruchi Sinha, Sabah Omar, Peter O’bare, Manuel Moro, Robert H. Gilman, Nick Harris, Henk D. F. H. Schallig
    PLOS ONE.2015; 10(9): e0136726.     CrossRef
  • Diagnosing malaria infected cells at the single cell level using focal plane array Fourier transform infrared imaging spectroscopy
    Bayden R. Wood, Keith. R. Bambery, Matthew W. A. Dixon, Leann Tilley, Michael J. Nasse, Eric Mattson, Carol J. Hirschmugl
    The Analyst.2014; 139(19): 4769.     CrossRef
  • Impact of a training course on the quality of malaria diagnosis by microscopy in Angola
    Sofia Moura, Cláudia Fançony, Clara Mirante, Marcela Neves, Luís Bernardino, Filomeno Fortes, Maria do Rosário Sambo, Miguel Brito
    Malaria Journal.2014;[Epub]     CrossRef
  • Clinical malaria diagnosis in pregnancy in relation to early perinatal mother‐to‐child transmission of HIV: a prospective cohort study
    AE Ezeamama, C Duggan, KP Manji, D Spiegelman, E Hertzmark, RJ Bosch, R Kupka, JO Okuma, R Kisenge, S Aboud, WW Fawzi
    HIV Medicine.2014; 15(5): 276.     CrossRef
  • Malaria and anaemia in pregnancy: a cross-sectional study of pregnant women in rural communities of Southeastern Nigeria
    Emmanuel O. Ugwu, Cyril C. Dim, Benjamin S. Uzochukwu, Emeka I. Iloghalu, Angela O. Ugwu
    International Health.2014; 6(2): 130.     CrossRef
  • Assessment of Fever in Returned Travelers
    Hyoung-Shik Shin
    Korean Journal of Medicine.2014; 86(4): 438.     CrossRef
  • Simple sample processing enhances malaria rapid diagnostic test performance
    K. M. Davis, L. E. Gibson, F. R. Haselton, D. W. Wright
    The Analyst.2014; 139(12): 3026.     CrossRef
  • Nested-PCR and a New ELISA-Based NovaLisa Test Kit for Malaria Diagnosis in an Endemic Area of Thailand
    Pimwan Thongdee, Wanna Chaijaroenkul, Jiraporn Kuesap, Kesara Na-Bangchang
    The Korean Journal of Parasitology.2014; 52(4): 377.     CrossRef
  • Application of loop-mediated isothermal amplification assay combined with lateral flow dipstick for detection of Plasmodium falciparum and Plasmodium vivax
    Suganya Yongkiettrakul, Wansadaj Jaroenram, Narong Arunrut, Wanwisa Chareanchim, Supicha Pannengpetch, Rungkarn Suebsing, Wansika Kiatpathomchai, Wichai Pornthanakasem, Yongyuth Yuthavong, Darin Kongkasuriyachai
    Parasitology International.2014; 63(6): 777.     CrossRef
  • LH750 hematology analyzers to identify malaria and dengue and distinguish them from other febrile illnesses
    P. Sharma, M. Bhargava, D. Sukhachev, S. Datta, C. Wattal
    International Journal of Laboratory Hematology.2014; 36(1): 45.     CrossRef
  • Evaluation of wondfo rapid diagnostic kit (Pf-HRP2/PAN-pLDH) for diagnosis of malaria by using nano-gold immunochromatographic assay
    Junlin Wu, Yunping Peng, Xiaoyun Liu, Wenmei Li, Shixing Tang
    Acta Parasitologica.2014;[Epub]     CrossRef
  • Detection and Quantification of Early-Stage Malaria Parasites in Laboratory Infected Erythrocytes by Attenuated Total Reflectance Infrared Spectroscopy and Multivariate Analysis
    Aazam Khoshmanesh, Matthew W. A. Dixon, Shannon Kenny, Leann Tilley, Don McNaughton, Bayden R. Wood
    Analytical Chemistry.2014; 86(9): 4379.     CrossRef
  • Differential expression of serum/plasma proteins in various infectious diseases: Specific or nonspecific signatures
    Sandipan Ray, Sandip K. Patel, Vipin Kumar, Jagruti Damahe, Sanjeeva Srivastava
    PROTEOMICS – Clinical Applications.2014; 8(1-2): 53.     CrossRef
  • Perceptions of malaria and acceptance of rapid diagnostic tests and related treatment practises among community members and health care providers in Greater Garissa, North Eastern Province, Kenya
    Emma Diggle, Ramin Asgary, Georgia Gore-Langton, Erupe Nahashon, James Mungai, Rebecca Harrison, Abdullahi Abagira, Katie Eves, Zoya Grigoryan, David Soti, Elizabeth Juma, Richard Allan
    Malaria Journal.2014;[Epub]     CrossRef
  • Evaluation of a Novel Magneto-Optical Method for the Detection of Malaria Parasites
    Ágnes Orbán, Ádám Butykai, András Molnár, Zsófia Pröhle, Gergö Fülöp, Tivadar Zelles, Wasan Forsyth, Danika Hill, Ivo Müller, Louis Schofield, Maria Rebelo, Thomas Hänscheid, Stephan Karl, István Kézsmárki, Stuart Alexander Ralph
    PLoS ONE.2014; 9(5): e96981.     CrossRef
  • Machine learning approach for automated screening of malaria parasite using light microscopic images
    Dev Kumar Das, Madhumala Ghosh, Mallika Pal, Asok K. Maiti, Chandan Chakraborty
    Micron.2013; 45: 97.     CrossRef
  • What is the best strategy for the prevention of transfusion-transmitted malaria in sub-Saharan African countries where malaria is endemic?
    Jobert Richie N Nansseu, Jean Jacques N Noubiap, Shalom Tchokfe Ndoula, Albert Frank M Zeh, Chavely Gwladys Monamele
    Malaria Journal.2013;[Epub]     CrossRef
  • Passive gravitational sedimentation of peripheral blood increases the sensitivity of microscopic detection of malaria
    Richard Davis, Trenden Flanigan, Eric Wilson
    Asian Pacific Journal of Tropical Medicine.2013; 6(7): 552.     CrossRef
  • Quantitative phase imaging and Raman micro-spectroscopy applied to Malaria
    Jacques Klossa, Benoit Wattelier, Teddy Happillon, Dominique Toubas, Lucie de Laulanie, Valérie Untereiner, Pierre Bon, Michel Manfait
    Diagnostic Pathology.2013;[Epub]     CrossRef
  • Assessment of Clinical Diagnosis, Microscopy, Rapid Diagnostic Tests, and Polymerase Chain Reaction in the Diagnosis of Plasmodium falciparum in Nigeria
    Olusola Ojurongbe, Olunike Olayeni Adegbosin, Sunday Samuel Taiwo, Oyebode Armstrong Terry Alli, Olugbenga Adekunle Olowe, Taiwo Adetola Ojurongbe, Oloyede Samuel Bolaji, Oluwaseyi Adegboyega Adeyeba
    Malaria Research and Treatment.2013; 2013: 1.     CrossRef
  • Cloning, overexpression, purification and characterization of Plasmodium knowlesi lactate dehydrogenase
    Vandana Singh, Deep C. Kaushal, Sushma Rathaur, Niraj Kumar, Nuzhat A. Kaushal
    Protein Expression and Purification.2012; 84(2): 195.     CrossRef
  • Real-time PCR diagnosis of Plasmodium vivax among blood donors
    Sergio Batista-dos-Santos, Milene Raiol, Sidney Santos, Maristela G Cunha, Ândrea Ribeiro-dos-Santos
    Malaria Journal.2012;[Epub]     CrossRef
  • Development of a Novel Fluorophore for Real-Time Biomonitoring System
    Hyun-Ok Song, Binna Lee, Ram Prasad Bhusal, Byounghun Park, Kyoungsik Yu, Chom-Kyu Chong, PyoYun Cho, Sung Yeon Kim, Hak Sung Kim, Hyun Park, Luzia Helena Carvalho
    PLoS ONE.2012; 7(11): e48459.     CrossRef
  • A preliminary comparative report of quantitative buffy coat and modified quantitative buffy coat with peripheral blood smear in malaria diagnosis
    Manali Kochareka, Sougat Sarkar, Debjani Dasgupta, Umesh Aigal
    Pathogens and Global Health.2012; 106(6): 335.     CrossRef
  • LABORATORY DIAGNOSIS OF MALARIA, A REVIEW
    Raghuveer C. V, Mangala Goneppanavar
    Journal of Evolution of Medical and Dental Sciences.2012; 1(4): 453.     CrossRef
  • HIV Infection and the Incidence of Malaria Among HIV-Exposed Children from Tanzania
    Amara E. Ezeamama, Donna Spiegelman, Ellen Hertzmark, Ronald J. Bosch, Karim P. Manji, Christopher Duggan, Roland Kupka, Melanie W. Lo, James O. Okuma, Rodrick Kisenge, Said Aboud, Wafaie W. Fawzi
    The Journal of Infectious Diseases.2012; 205(10): 1486.     CrossRef
  • Prospective study on severe malaria among in-patients at Bombo regional hospital, Tanga, north-eastern Tanzania
    Hamisi A Msangeni, Mathias L Kamugisha, Samuel H Sembuche, Ezekiel K Malecela, Juma A Akida, Filbert F Temba, Bruno P Mmbando, Martha M Lemnge
    BMC Infectious Diseases.2011;[Epub]     CrossRef
  • Clinical review of malaria for the emergency physician
    Laura Janneck, Alex Koyfman, James Kimo Takayesu
    African Journal of Emergency Medicine.2011; 1(3): 126.     CrossRef
  • Informed decision-making before changing to RDT: a comparison of microscopy, rapid diagnostic test and molecular techniques for the diagnosis and identification of malaria parasites in Kassala, eastern Sudan
    Mamoun M. M. Osman, Bakri Y. M. Nour, Mohamed F. Sedig, Laura De Bes, Adil M. Babikir, Ahmed A. Mohamedani, Petra F. Mens
    Tropical Medicine & International Health.2010; 15(12): 1442.     CrossRef
  • Are rapid diagnostic tests more accurate in diagnosis of plasmodium falciparum malaria compared to microscopy at rural health centres?
    Vincent Batwala, Pascal Magnussen, Fred Nuwaha
    Malaria Journal.2010;[Epub]     CrossRef
  • 30,774 View
  • 1,814 Download
  • Crossref