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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
Korean J Parasitol 2019;57(1):21-25.
Published online February 26, 2019
DOI: https://doi.org/10.3347/kjp.2019.57.1.21
Trichomoniasis is the most common curable sexually-transmitted infection. Most Trichomonas vaginalis-infected men are asymptomatic and can remain undiagnosed and untreated, and this has been thought to result in chronic persistent prostatic infection. Chronic inflammation is regarded as the major factor in the pathogenesis and progression of benign prostatic hyperplasia (BPH) and prostatic cancer (PCa). The aim of this study is to identify seropositivity to T. vaginalis in men with prostate tumors (BPH or PCa) visited to Hanyang University Hospital. A total of 183 men were enrolled between October 2013 and November 2014. They consisted of 139 with BPH (mean age: 64.0 ± 0.07) and 44 with prostate cancer (mean age: 73.3±0.18). We carried out ELISA to identify the seropositivity to T. vaginalis. Mixed lysate antigen extracted from 8 strains of T. vaginalis was used in the ELISA. Also 58 male outpatients visited to Health Promotion Center in Hanyang University Hospital were evaluated for comparing group. As a results, seropositivity to T. vaginalis in patients with prostatic diseases was 19.7% (BPH: 18.7%, PCa: 22.7%) and it was significantly higher than the 1.7% of the comparing healthy group (P = 0.001). Therefore, prostatic tumor showed higher seropositivity against T. vaginalis than normal men. As far as we know, this is the first report about seroprevalence in prostatic tumor in Korea.

Citations

Citations to this article as recorded by  Crossref logo
  • The Past, Present, and Future in the Diagnosis of a Neglected Sexually Transmitted Infection: Trichomoniasis
    Alexandra Ibáñez-Escribano, Juan José Nogal-Ruiz
    Pathogens.2024; 13(2): 126.     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 responses during trichomoniasis: The role of Toll‐like receptors and inflammasomes
    Abdollah Jafarzadeh, Maryam Nemati, Ehsan Salarkia, Sonal Yadav, Najmeh Aminizadeh, Sara Jafarzadeh, Manisha Yadav
    Parasite Immunology.2023;[Epub]     CrossRef
  • No Association of Trichomonas vaginalis Seropositivity with Advanced Prostate Cancer Risk in the Multiethnic Cohort: A Nested Case-Control Study
    Michelle Nagata, Anne Tome, Kami White, Lynne R. Wilkens, Song-Yi Park, Loïc Le Marchand, Christopher Haiman, Brenda Y. Hernandez
    Cancers.2023; 15(21): 5194.     CrossRef
  • Identification of Signature Genes and Construction of an Artificial Neural Network Model of Prostate Cancer
    Hongye Dong, Xu Wang, Kalidoss Rajakani
    Journal of Healthcare Engineering.2022; 2022: 1.     CrossRef
  • Multiple pathogens and prostate cancer
    James S. Lawson, Wendy K. Glenn
    Infectious Agents and Cancer.2022;[Epub]     CrossRef
  • Trichomonas vaginalis serostatus and prostate cancer risk in Egypt: a case-control study
    Nora E. Saleh, Samar M. Alhusseiny, Wafaa M. El-Zayady, Engy M. Aboelnaga, Wafaa N. El-beshbishi, Yasser M. Saleh, Hala S. Abou-ElWafa, Samar N. El-Beshbishi
    Parasitology Research.2021; 120(4): 1379.     CrossRef
  • The Role of Microbial Factors in Prostate Cancer Development—An Up-to-Date Review
    Karolina Garbas, Piotr Zapała, Łukasz Zapała, Piotr Radziszewski
    Journal of Clinical Medicine.2021; 10(20): 4772.     CrossRef
  • Involvement of Macrophages in Proliferation of Prostate Cancer Cells Infected with Trichomonas vaginalis
    Kyu-Shik Kim, Hong-Sang Moon, Sang-Su Kim, Jae-Sook Ryu
    The Korean Journal of Parasitology.2021; 59(6): 557.     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
  • Is Trichomonas vaginalis a Risk Factor for Prostate Cancer? A Systematic Review and Meta-analysis
    Gianpaolo Perletti, Vittorio Magri, Louise Beckers-Perletti, Alberto Trinchieri, Konstantinos Stamatiou
    Hellenic Urology.2021; 33(1): 12.     CrossRef
  • IL-6 produced by prostate epithelial cells stimulated with Trichomonas vaginalis promotes proliferation of prostate cancer cells by inducing M2 polarization of THP-1-derived macrophages
    Ik-Hwan Han, Hyun-Ouk Song, Jae-Sook Ryu, Michael H. Hsieh
    PLOS Neglected Tropical Diseases.2020; 14(3): e0008126.     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
  • The Crosstalk between Prostate Cancer and Microbiota Inflammation: Nutraceutical Products Are Useful to Balance This Interplay?
    Felice Crocetto, Mariarosaria Boccellino, Biagio Barone, Erika Di Zazzo, Antonella Sciarra, Giovanni Galasso, Giuliana Settembre, Lucio Quagliuolo, Ciro Imbimbo, Silvia Boffo, Italo Francesco Angelillo, Marina Di Domenico
    Nutrients.2020; 12(9): 2648.     CrossRef
  • 9,237 View
  • 152 Download
  • 12 Web of Science
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Seropositivity of Toxoplasma gondii and Toxocara spp. in Children with Cryptogenic Epilepsy, Benha, Egypt
Maysa Ahmad Eraky, Soha Abdel-Hady, Karim Fetouh Abdallah
Korean J Parasitol 2016;54(3):335-338.
Published online June 30, 2016
DOI: https://doi.org/10.3347/kjp.2016.54.3.335
The present study aimed to investigate the possible association of Toxoplasma gondii and Toxocara spp. infections with cryptogenic epilepsy in children. The study was carried out between June 2014 and March 2015. T otal 90 children (40 with cryptogenic epilepsy, 30 with non-cryptogenic epilepsy, and 20 healthy control children) were evaluated to determine the anti-Toxocara and anti-T . gondii IgG seropositivity using ELISA kits. Epileptic cases were selected from those attending the pediatrics outpatient clinic of Benha University Hospital, Pediatrics Neurology Unit, and from Benha Specialized Hospital of children. The results showed that the level of anti-T . gondii IgG seropositivity was significantly higher among children with cryptogenic epilepsy (20%) than among children with non-cryptogenic children (0%). In healthy controls (10%), there was no association between toxocariasis seropositivity and cryptogenic epilepsy (only 5.7%; 4 out of 70 cases) among cases and 10% (2 out of 20) among controls. Among toxocariasis IgG positive cases, 3 (7.5%) were cryptogenic, and only 1 (3.3%) was non-cryptogenic. These statistically significant results support the association between T . gondii infection and cryptogenic epilepsy while deny this association with toxocariasis.

Citations

Citations to this article as recorded by  Crossref logo
  • Evaluation of Toxoplasma gondii in the Etiology of Cryptogenic Epilepsy: A Case-control Study
    Selahattin Aydemir, Milad Torkamanian Afshar, Özlem Sarı Torkamanian Afshar, Zeynep Taş Cengiz, Mustafa Kiraz, Caner Baydar, Hasan Yılmaz
    Archives Of Epilepsy.2024; : 39.     CrossRef
  • Effects of diet and ovariectomy on Toxoplasma gondii brain infection: functional alterations and neuronal loss in rats
    Nene Ahidjo, Paul F Seke Etet, Leonard Ngarka, Frederic Maidawa Yaya, Ethel W Ndianteng, Aude L Eyenga Nna, Luc Yvan Meka’a Zang, Christelle Kemmo, Caroline N C Nwasike, Floriane G Yonkeu Tatchou, Wepnyu Y Njamnshi, Leonard N Nfor, Patrick V Tsouh Fokou,
    Brain Communications.2024;[Epub]     CrossRef
  • Common infectious and parasitic diseases as a cause of seizures: geographic distribution and contribution to the burden of epilepsy
    Elza Márcia T. Yacubian, Angelina Kakooza‐Mwesige, Gagandeep Singh, Arturo Carpio, Nathália V. de Figueiredo, Ricardo Lutzky Saute, Tissiana Marques de Haes
    Epileptic Disorders.2022; 24(6): 994.     CrossRef
  • Seroprevalence and Genetic Characterization of Toxoplasma gondii among Children with Neurodevelopmental Disorders in Egypt
    Sara M. Elzeky, Nairmen Nabih, Aida A. Abdel-Magied, Dina S. Abdelmagid, Aya E. Handoussa, Marwa M. Hamouda, Wei Wang
    Journal of Tropical Medicine.2022; 2022: 1.     CrossRef
  • Exposure to Toxocara Canis is not Associated with New-Onset Epilepsy
    Vivek Rishi, Rajveer Singh, Manoj Kumar Goyal, Manish Modi, Vivek Garg, J. S. Thakur, R. K. Sehgal, N. Khandelwal, Gourav Jain, Amith S. Kumar, Aditya Choudhary, Sudesh Prabhakar, Vivek Lal
    Neurology India.2022; 70(6): 2383.     CrossRef
  • Cerebral Toxocariasis as a Cause of Epilepsy: A Pediatric Case
    Grazia Bossi, Raffaele Bruno, Stefano Novati, Roberta Maserati, Georgia Mussati, Mariasole Prevedoni Gorone, Edoardo Vecchio Nepita, Corrado Regalbuto, Gioia Gola, Anna Maria Simoncelli, Antonella Bruno, Paola Musso, Edoardo Clerici, Gian Luigi Marseglia
    Neuropediatrics.2021; 52(02): 142.     CrossRef
  • Case-Control Study to Assess the Association between Epilepsy and Toxocara Infection/Exposure
    Ali Alizadeh Khatir, Mahdi Sepidarkish, Mohammad Reza Rajabalizadeh, Solmaz Alizadeh Moghaddam, Saeed Aghapour, Saeed Mehravar, Peter J. Hotez, Robin B. Gasser, Ali Rostami
    Microorganisms.2021; 9(10): 2091.     CrossRef
  • Neurological and Neurobehavioral Disorders Associated with Toxoplasma gondii Infection in Humans
    Maxwell A. Virus, Evie G. Ehrhorn, LeeAnna M. Lui, Paul H. Davis, Hassen Mamo
    Journal of Parasitology Research.2021; 2021: 1.     CrossRef
  • Toxoplasma infection and risk of epilepsy: A case-control study of incident patients
    Ali Alizadeh Khatir, Solmaz Alizadeh Moghaddam, Mustafa Almukhtar, Hossein Ghorbani, Arefeh Babazadeh, Saeed Mehravar, Ali Rostami
    Microbial Pathogenesis.2021; 161: 105302.     CrossRef
  • Frequency ofToxocara canisantibodies in Mexican paediatric patients with epilepsy
    M.d.L. Caballero-García, J. Simón-Salvador, J.C. Hernández-Aguilar, A. Reyes-Lopez, B. Nogueda-Torres, E. Jiménez-Cardoso
    Journal of Helminthology.2020;[Epub]     CrossRef
  • A review on toxoplasmosis in humans and animals from Egypt
    I. E. Abbas, I. Villena, J. P. Dubey
    Parasitology.2020; 147(2): 135.     CrossRef
  • Zoonotic and vector-borne parasites and epilepsy in low-income and middle-income countries
    Gagandeep Singh, Samuel A. Angwafor, Alfred K. Njamnshi, Henry Fraimow, Josemir W. Sander
    Nature Reviews Neurology.2020; 16(6): 333.     CrossRef
  • Effects of Toxoplasma gondii infection and schizophrenia comorbidity on serum lipid profile: A population retrospective study from Eastern China
    Fei Xu, Xinyu Ma, Yuwei Zhu, Arjen Sutterland, Ruitang Cheng, Sunhan Miao, Jialu Chen, Liying Qiu, Yonghua Zhou
    Microbial Pathogenesis.2020; 149: 104587.     CrossRef
  • An updated meta-analysis of the association between Toxoplasma gondii infection and risk of epilepsy
    Maryam Sadeghi, Seyed Mohammad Riahi, Mona Mohammadi, Vafa Saber, Somayeh Aghamolaie, Solmaz Alizadeh Moghaddam, Shima Aghaei, Mostafa Javanian, H Ray Gamble, Ali Rostami
    Transactions of The Royal Society of Tropical Medicine and Hygiene.2019; 113(8): 453.     CrossRef
  • Updated evidence of the association between toxocariasis and epilepsy: Systematic review and meta-analysis
    Jaime Luna, Calogero Edoardo Cicero, Guillaume Rateau, Graziella Quattrocchi, Benoit Marin, Elisa Bruno, François Dalmay, Michel Druet-Cabanac, Alessandra Nicoletti, Pierre-Marie Preux, Agnes Fleury
    PLOS Neglected Tropical Diseases.2018; 12(7): e0006665.     CrossRef
  • Seroprevalence of Toxoplasma gondii infection in children with central nervous system disorders in Mansoura, Egypt: a case–control study
    Samar N El-Beshbishi, Nora L El-Tantawy, Sara M Elzeky, Khalid F Abdalaziz, Raefa A Atia
    Transactions of The Royal Society of Tropical Medicine and Hygiene.2018;[Epub]     CrossRef
  • Toxocariasis in humans in Africa – A systematic review
    Felix Lötsch, Rieke Vingerling, Rene Spijker, Martin Peter Grobusch
    Travel Medicine and Infectious Disease.2017; 20: 15.     CrossRef
  • 10,047 View
  • 129 Download
  • 24 Web of Science
  • Crossref
Original Articles
Seropositivity of Toxoplasmosis in Pregnant Women by ELISA at Minia University Hospital, Egypt
Amany M. Kamal, Azza K. Ahmed, Manal Z. M. Abdellatif, Mohamed Tawfik, Ebtesam E. Hassan
Korean J Parasitol 2015;53(5):605-610.
Published online October 29, 2015
DOI: https://doi.org/10.3347/kjp.2015.53.5.605
Toxoplasmosis is considered as an important risk factor for bad obstetric history (BOH) and one of the major causes of congenitally acquired infections. The present study aimed to estimate the seropositivity of T. gondii infection and associated risk factors among the attendees of high risk pregnancy and low risk antenatal care clinic of Minia Maternity and Pediatric University Hospital, Minia, Egypt. The study was carried out from April 2013 to April 2014 through 2 phases, the first phase was case-control study, and the second phase was follow-up with intervention. A total of 120 high risk pregnant and 120 normal pregnant females were submitted to clinical examinations, serological screening for anti-Toxoplasma IgM and IgG antibodies by ELISA, and an interview questionnaire. Seropositive cases were subjected to spiramycin course treatment. The results showed that the seroprevalence of toxoplasmosis in high-risk pregnancy group was 50.8%, which was significantly different from that of normal pregnancy group (P < 0.05). Analysis of seropositive women in relation to BOH showed that abortion was the commonest form of the pregnancy wastage (56.5%). The high prevalence of T. gondii seropositive cases was observed in the age group of 21-30 years. Post-delivery adverse outcome was observed in 80.3% of high-risk pregnancy group compared to 20% of normal pregnancy group. There was a statistically significant relationship between seropositivity and living in rural area, low socioeconomic level, and undercooked meat consumption (P<0.05). Serological screening for anti-Toxoplasma antibodies should be routine tests especially among high-risk pregnant women.

Citations

Citations to this article as recorded by  Crossref logo
  • Seroprevalence of Toxoplasma gondii Antibodies and Associated Risk Factors Among Women in Zakho City, Iraq
    Kalthom M Mustafa, Ahmed B Mohammed, Wijdan M.S. Mero
    Cureus.2024;[Epub]     CrossRef
  • Interplay between cross sectional analysis of risk factors associated with Toxoplasma gondii infection in pregnant women and their domestic cats
    Eman A. A. Hassanen, Dennis N. Makau, Mohamed Afifi, Omar A. Al-Jabr, Mohammed Abdulrahman Alshahrani, Ahmed Saif, Reham G. A. Anter, Wafaa M. El-Neshwy, Doaa Ibrahim, Rasha M. M. Abou Elez
    Frontiers in Veterinary Science.2023;[Epub]     CrossRef
  • Upregulation of IL-33, CCL2, and CXCL16 levels in Brazilian pregnant women infected by Toxoplasma gondii
    Priscilla Vilela dos Santos, Débora Nonato Miranda de Toledo, Nathalia Sernizon Guimarães, Luiza Oliveira Perucci, Valter Ferreira de Andrade-Neto, André Talvani
    Acta Tropica.2023; 243: 106931.     CrossRef
  • Latent Toxoplasmosis is Associated with Depression and Suicidal Behavior
    Ahmed M. Kamal, Amany M. Kamal, Aliaa S. Abd El-Fatah, Mina M. Rizk, Eptesam E. Hassan
    Archives of Suicide Research.2022; 26(2): 819.     CrossRef
  • Detection of toxoplasmosis in aborted women in Alexandria, Egypt using ELISA and PCR
    Mona Hassan El-Sayad, Aziza Ibrahim Salem, Hisham Fazary, Haneen Nawaf Alzainny, Naglaa Fathi Abd El-Latif
    Journal of Parasitic Diseases.2021; 45(2): 539.     CrossRef
  • Seroprevalence of Neospora caninum and Toxoplasma gondii IgG and IgM antibodies among buffaloes and cattle from Menoufia Province, Egypt
    Hany M. Ibrahim, Adel A. H. Abdel-Rahman, Nora M. Bishr
    Journal of Parasitic Diseases.2021; 45(4): 952.     CrossRef
  • Distribution of integrons and phylogenetic groups among Escherichia coli causing community-acquired urinary tract infection in Upper Egypt
    Eman M. Farahat, Noha A. Hassuna, Adel M. Hammad, Medhat Abdel Fattah, Ahmed S. Khairalla
    Canadian Journal of Microbiology.2021; 67(6): 451.     CrossRef
  • Evaluation of soluble CD279 (sCD279) and CD274 (sCD274) in Iraqi patients with Acute Myeloid Leukemia (AML) with Toxoplasmosis
    Ali A. Issa, Ali N. Yaseen, Muhammed A. H. Aldabagh
    IOP Conference Series: Earth and Environmental Science.2021; 790(1): 012065.     CrossRef
  • Toxoplasma gondii infection and spontaneous abortion: A systematic review and meta-analysis
    Narges Kalantari, Tahmineh Gorgani-Firouzjaee, Zahra Moulana, Mohammad Chehrazi, Salman Ghaffari
    Microbial Pathogenesis.2021; 158: 105070.     CrossRef
  • Toxoplasmosis in immunocompetent Saudi women: Correlation with vitamin D
    Zafar Rasheed, Ali Shariq, Ghaida B AlQefari, Ghayda S Alwahbi, Amal I Aljuaythin, Fidaa S Alsuhaibani, Daliyah F Alotaibi, Shahad S Aljohani, Ruqiah Alghasham, Thamir Alsaeed, Nada A Alharbi, Osamah Al Rugaie, Waleed Al Abdulmonem, Osama F Sharaf
    Women's Health.2021;[Epub]     CrossRef
  • Toxoplasma gondii seropositivity and the associated risk factors in sheep and pregnant women in El-Minya Governorate, Egypt
    Abdelbaset E. Abdelbaset, Maha I. Hamed, Mostafa F. N. Abushahba, Mohamed S. Rawy, Amal S. M. Sayed, Jeffrey J. Adamovicz
    Veterinary World.2020; 13(1): 54.     CrossRef
  • A review on toxoplasmosis in humans and animals from Egypt
    I. E. Abbas, I. Villena, J. P. Dubey
    Parasitology.2020; 147(2): 135.     CrossRef
  • The global seroprevalence of anti-Toxoplasma gondii antibodies in women who had spontaneous abortion: A systematic review and meta-analysis
    Tooran Nayeri, Shahabeddin Sarvi, Mahmood Moosazadeh, Afsaneh Amouei, Zahra Hosseininejad, Ahmad Daryani, Maria Angeles Gómez-Morales
    PLOS Neglected Tropical Diseases.2020; 14(3): e0008103.     CrossRef
  • Risk factors associated with seropositivity for Toxoplasma gondii in population-based studies among immunocompromised patients (pregnant women, HIV patients and children) in West African countries, Cameroon and Gabon: a meta-analysis
    Paul Olalekan Odeniran, Kehinde Foluke Omolabi, Isaiah Oluwafemi Ademola
    Acta Tropica.2020; 209: 105544.     CrossRef
  • Serological prevalence of toxoplasmosis in pregnant women in Luanda (Angola): Geospatial distribution and its association with socio-demographic and clinical-obstetric determinants
    Amélia Nkutxi Vueba, Clarissa Perez Faria, Ricardo Almendra, Paula Santana, Maria do Céu Sousa, Adriana Calderaro
    PLOS ONE.2020; 15(11): e0241908.     CrossRef
  • Clinico-epidemiological and sociodemographic profile of HIV/AIDS patients who are co-infected with Toxoplasma gondii in the border region of Brazil
    JANIELLE C. MORO, NEIDE M. MOREIRA
    Anais da Academia Brasileira de Ciências.2020;[Epub]     CrossRef
  • Potential risk factors associated with seropositivity for Toxoplasma gondii among pregnant women and HIV infected individuals in Ethiopia: A systematic review and meta-analysis
    Zewdu Seyoum Tarekegn, Haileyesus Dejene, Agerie Addisu, Shimelis Dagnachew, Olaf Horstick
    PLOS Neglected Tropical Diseases.2020; 14(12): e0008944.     CrossRef
  • Toxoplasma gondii infection and toxoplasmosis in North Africa: a review
    Mariem Rouatbi, Safa Amairia, Yosra Amdouni, Mohamed Anis Boussaadoun, Ouarda Ayadi, Amira Adel Taha Al-Hosary, Mourad Rekik, Rym Ben Abdallah, Karim Aoun, Mohamed Aziz Darghouth, Barbara Wieland, Mohamed Gharbi
    Parasite.2019; 26: 6.     CrossRef
  • BCG scar, socioeconomic and nutritional status: a study of newborns in urban area of Makassar, Indonesia
    Aldian Irma Amaruddin, Sitti Wahyuni, Firdaus Hamid, Maisuri T. Chalid, Maria Yazdanbakhsh, Erliyani Sartono
    Tropical Medicine & International Health.2019; 24(6): 736.     CrossRef
  • Conhecimento e comportamento preventivo de gestantes sobre Toxoplasmose no município de Imperatriz, Maranhão, Brasil
    Ivone Pereira da Silva Moura, Ilma Pastana Ferreira, Altem Nascimento Pontes, Cléa Nazaré Carneiro Bichara
    Ciência & Saúde Coletiva.2019; 24(10): 3933.     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
  • Seroprevalence of Toxoplasma gondii among pregnant women attending antenatal clinics at Hawassa University comprehensive specialized and Yirgalem General Hospitals, in Southern Ethiopia
    Demissie Assegu Fenta
    BMC Infectious Diseases.2019;[Epub]     CrossRef
  • Toxoplasma gondii seroprevalence among pregnant women attending antenatal clinic in Northern Tanzania
    Eliakimu Paul, Ireen Kiwelu, Blandina Mmbaga, Rebeka Nazareth, Elias Sabuni, Athanasia Maro, Arnold Ndaro, Jo E. B. Halliday, Jaffu Chilongola
    Tropical Medicine and Health.2018;[Epub]     CrossRef
  • Seroprevalence and associated risk factors of Toxoplasma gondii among Manchu pregnant women in northeastern China
    Ruo-Lan Jiang, Ling-Hui Ma, Zhen-Rong Ma, Guangyu Hou, Quan Zhao, Xiang Wu
    Microbial Pathogenesis.2018; 123: 398.     CrossRef
  • Seroprevalence and potential risk factors of T. gondii infection in pregnant women attending antenatal care at Bonga Hospital, Southwestern Ethiopia
    Jalel Negero, Moti Yohannes, Kifle Woldemichael, Dechassa Tegegne
    International Journal of Infectious Diseases.2017; 57: 44.     CrossRef
  • Comparative and analytical study on active toxoplasmosis to assess the IgG avidity in correlation to serological profile in a cohort of Egyptian patients
    Al Shaimaa M. R. Hamed, Shadia H. Omar, Maha M. A. Basyoni, Abeer S. El Antably, Engy El Khateeb, Abdulla Y. El Kateb
    Comparative Clinical Pathology.2017; 26(5): 1157.     CrossRef
  • Molecular and serological prevalence of Toxoplasma gondii in pregnant women and sheep in Egypt
    Hany M. Ibrahim, Azza H. Mohamed, Ahmed A. El-Sharaawy, Hend E. El-Shqanqery
    Asian Pacific Journal of Tropical Medicine.2017; 10(10): 996.     CrossRef
  • Seroprevalence of Anti-Toxoplasma gondiiAntibodies Among Lebanese Pregnant Women
    Hasan Nahouli, Nour El Arnaout, Elias Chalhoub, Elie Anastadiadis, Hiba El Hajj
    Vector-Borne and Zoonotic Diseases.2017; 17(12): 785.     CrossRef
  • Comparison of Placenta PCR and Maternal Serology of Aborted Women for Detection of Toxoplasma gondii in Ardabil, Iran
    Somaie Matin, Gholamreza Shahbazi, Shervin Tabrizian Namin, Rouhallah Moradpour, Farideh Feizi, Hadi Piri-dogahe
    The Korean Journal of Parasitology.2017; 55(6): 607.     CrossRef
  • Is Toxoplasma Gondii Infection a Risk Factor for Leukemia? An Evidence-Based Meta-Analysis
    Yi Huang, Yu Huang, Aoshuang Chang, Jishi Wang, Xiaoqing Zeng, Jiahong Wu
    Medical Science Monitor.2016; 22: 1547.     CrossRef
  • 13,802 View
  • 155 Download
  • 33 Web of Science
  • Crossref
Relationship between Antibody-Positive Rate against Plasmodium vivax Circumsporozoite Protein and Incidence of Malaria
Hyeong-Woo Lee, Yoon-Joong Kang, Shin-Hyeong Cho, Byoung-Kuk Na, Jhang Ho Pak, Ho-Woo Nam, Yun-Kyu Park, Youngjoo Sohn, Tong-Soo Kim
Korean J Parasitol 2015;53(2):169-175.
Published online April 22, 2015
DOI: https://doi.org/10.3347/kjp.2015.53.2.169
The relationship between anti-Plasmodium vivax circumsporozoite protein (CSP) antibody levels and the prevalence of malaria in epidemic areas of South Korea was evaluated. Blood samples were collected from inhabitants of Gimpo-si (city), Paju-si, and Yeoncheon-gun (county) in Gyeonggi-do (province), as well as Cheorwon-gun in Gangwon-do from November to December 2004. Microscopic examinations were used to identify malaria parasites. ELISA was used to quantitate anti-circumsporozoite protein (CSP) antibodies against P. vivax. A total of 1,774 blood samples were collected. The overall CSP-ELISA-positive rate was 7.7% (n=139). The annual parasite incidences (APIs) in these areas gradually decreased from 2004 to 2005 (1.09 and 0.80, respectively). The positive rate in Gimpo (10.4%, 44/425) was the highest identified by CSP-ELISA. The highest API was found in Yeoncheon, followed by Cheorwon, Paju, and Gimpo in both years. The positive rates of CSP-ELISA were closely related to the APIs in the study areas. These results suggest that seroepidemiological studies based on CSP may be helpful in estimating the malaria prevalence in certain areas. In addition, this assay can be used to establish and evaluate malaria control and eradication programs in affected areas.

Citations

Citations to this article as recorded by  Crossref logo
  • Updated global distribution of Plasmodium vivax circumsporozoite protein variants and their correlation with vector susceptibility: A systematic review and meta-analysis
    Marrara P. Sampaio, Marcelo Cerilo-Filho, Yasmin de A․G․do Amaral, Maria Naely G. Almeida, Rayanne I. Correa, Dulce J.V. Fernando, Nathália F. Reis, Leonardo A. Miceli, José R.S. Silva, Luciane M. Storti-Melo, Andréa R.S. Baptista, Ricardo L.D. Machado
    Acta Tropica.2025; 261: 107508.     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
  • 9,663 View
  • 124 Download
  • 2 Web of Science
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Seroprevalence of Plasmodium vivax in the Republic of Korea (2003-2005) using Indirect Fluorescent Antibody Test
Tong-Soo Kim, Yoon-Joong Kang, Won-Ja Lee, Byoung-Kuk Na, Sung-Ung Moon, Seok Ho Cha, Sung-Keun Lee, Yun-Kyu Park, Jhang-Ho Pak, Pyo Yun Cho, Youngjoo Sohn, Hyeong-Woo Lee
Korean J Parasitol 2014;52(1):1-7.
Published online February 19, 2014
DOI: https://doi.org/10.3347/kjp.2014.52.1.1

Plasmodium vivax reemerged in the Republic of Korea (ROK) in 1993, and is likely to continue to affect public health. The purpose of this study was to measure levels of anti-P. vivax antibodies using indirect fluorescent antibody test (IFAT) in border areas of ROK, to determine the seroprevalence of malaria (2003-2005) and to plan effective control strategies. Blood samples of the inhabitants in Gimpo-si, Paju-si, and Yeoncheon-gun (Gyeonggi-do), and Cheorwon-gun (Gangwon-do) were collected and kept in Korea Centers for Disease Control and Prevention (KCDC). Out of a total of 1,774 serum samples tested, the overall seropositivity was 0.94% (n=17). The seropositivity was the highest in Paju-si (1.9%, 7/372), followed by Gimpo-si (1.4%, 6/425), Yeoncheon-gun (0.67%, 3/451), and Cheorwon-gun (0.19%, 1/526). The annual parasite incidence (API) in these areas gradually decreased from 2003 to 2005 (1.69, 1.09, and 0.80 in 2003, 2004, and 2005, respectively). The highest API was found in Yeoncheon-gun, followed by Cheorwon-gun, Paju-si, and Gimpo-si. The API ranking in these areas did not change over the 3 years. The seropositivity of Gimpo-si showed a strong linear relationship with the API of 2005 (r=0.9983, P=0.036). Seropositivity data obtained using IFAT may be useful for understanding malaria prevalence of relevant years, predicting future transmission of malaria, and for establishing and evaluating malaria control programs in affected areas.

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  • 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
  • 9,617 View
  • 98 Download
  • 1 Web of Science
  • Crossref