Parasites, Hosts and Diseases

"Nimit Morakote"

Brief Communications

High Prevalence of Haplorchiasis in Nan and Lampang Provinces, Thailand, Proven by Adult Worm Recovery from Suspected Opisthorchiasis Cases: Adulsak Wijit, Nimit Morakote, Jaewwaew Klinchid; Korean J Parasitol 2013;51(6):767-769.
Published online December 31, 2013; DOI: https://doi.org/10.3347/kjp.2013.51.6.767

Abstract
PDF

Opisthorchiasis, a risk factor for cholangiocarcinoma in humans, is of public health importance in Thailand. The Annual Surveillance Reports from Nan and Lampang Provinces, Thailand, for the year 2011 showed an opisthorchiasis prevalence of over 70% by recovery of eggs in the feces. This study investigated whether most cases are actually due to minute intestinal flukes (MIF) rather than Opisthorchis viverrini, as the eggs of both can hardly be differentiated by morphology. Fifty and 100 cases from residents in Nan and Lampang, respectively, had stools positive for eggs initially assumed to be those of O. viverrini. Each patient was given praziquantel at 40 mg/kg in a single dose. After 2 hr, 30-45 ml of the purgative magnesium sulfate was given, and stools were collected up to 4 times sequentially. The stools were examined for adult worms by simple sedimentation. It was found that 39 of 50 cases (78.0%) from Nan Province had Haplorchis taichui, with intensities ranging from 5 to 1,250 with an average of 62 worms/case. Taenia saginata (7 cases) and Enterobius vermicularis (1 case) were other helminths recovered as the co-infectants. In Lampang Province, H. taichui was recovered from 69 cases (69.0%). The number of flukes recovered ranged from 1 to 4,277, with an average of 326 worms/case. Four cases had Phaneropsolus bonnei, and 10 T. saginata as the co-infectants. Adult specimens of O. viverrini were not recovered from any stool. Clearly, MIF infection, especially haplorchiasis, is more common in northern Thailand. These findings should encourage the Public Health Office to employ more specific tools than Kato's method for surveillance of opisthorchiasis in Thailand.

Citations

Citations to this article as recorded by

Prevalence and Epidemiological Patterns of Enterobius vermicularis Infection in Thailand: A Systematic Review and Meta-Analysis
Jurairat Jongthawin, Aongart Mahittikorn, Apiporn Thinkhamrop Suwannatrai, Chutima Rattanawan, Kinley Wangdi, Frederick Ramirez Masangkay, Manas Kotepui
Medical Sciences.2025; 13(4): 207. CrossRef
Study of the population genetic structure of Opisthorchis-like eggs in northern Thailand using mitochondrial genes
Picha Suwannahitatorn, Mathirut Mungthin, Ittisak Subrungruang, Lakhanawan Charoensuk, Nithikoon Aksorn, Saiwasan Buathong, Krystyna Cwiklinski
PLOS Neglected Tropical Diseases.2024; 18(8): e0012445. CrossRef
Gastrointestinal Helminthic Infection among the Population in Northern Thailand
Ampas Wisetmora, Oranard Wattanawong, Adulsak Wijit, Jutikarn Phukowluan, Ampol Nachairan, Prueksarawuth Jaksuay, Sivapong Sungpradit, Nuttapon Ekobol, Thidarut Boonmars, Alisa Boonsuya, Phornphitcha Pechdee, Chutharat Thanchonnang, Nav La, Nathkapach K.
Acta Parasitologica.2024; 69(3): 1648. CrossRef
Model-based spatial-temporal mapping of opisthorchiasis in endemic countries of Southeast Asia
Ting-Ting Zhao, Yi-Jing Feng, Pham Ngoc Doanh, Somphou Sayasone, Virak Khieu, Choosak Nithikathkul, Men-Bao Qian, Yuan-Tao Hao, Ying-Si Lai
eLife.2021;[Epub] CrossRef
Adenosine Suppresses Cholangiocarcinoma Cell Growth and Invasion in Equilibrative Nucleoside Transporters-Dependent Pathway
Kornkamon Lertsuwan, Supathra Phoaubon, Nathapol Tasnawijitwong, Jomnarong Lertsuwan
International Journal of Molecular Sciences.2020; 21(3): 814. CrossRef
Intestinal parasites in rural communities in Nan Province, Thailand: changes in bacterial gut microbiota associated with minute intestinal fluke infection
Ajala Prommi, Pinidphon Prombutara, Dorn Watthanakulpanich, Poom Adisakwattana, Teera Kusolsuk, Tippayarat Yoonuan, Akkarin Poodeepiyasawat, Nirundorn Homsuwan, Samreong Prummongkol, Malee Tanita, Sungkhom Rattanapikul, Chuanphot Thinphovong, Anamika Krit
Parasitology.2020; 147(9): 972. CrossRef
Genetic Differentiation of Opisthorchis-Like Eggs in Northern Thailand Using Stool Specimens Under National Strategic Plan to Control Liver Fluke Infection and Cholangiocarcinoma
Saiwasan Buathong, Kateitsaray Phaiphilai, Toon Ruang-areerate, Naruemon Sitthichot, Thanyapit Thita, Mathirut Mungthin, Picha Suwannahitatorn
The American Journal of Tropical Medicine and Hygiene.2020; 103(3): 1118. CrossRef
Parasitic infections in relation to practices and knowledge in a rural village in Northern Thailand with emphasis on fish-borne trematode infection
K. Chaisiri, C. Jollivet, P. Della Rossa, S. Sanguankiat, D. Wattanakulpanich, C. Lajaunie, A. Binot, M. Tanita, S. Rattanapikul, D. Sutdan, S. Morand, A. Ribas
Epidemiology and Infection.2019;[Epub] CrossRef
Fishborne zoonotic heterophyid infections: An update
Jong-Yil Chai, Bong-Kwang Jung
Food and Waterborne Parasitology.2017; 8-9: 33. CrossRef
Molecular discrimination of Opisthorchis-like eggs from residents in a rural community of central Thailand
Saiwasan Buathong, Saovanee Leelayoova, Mathirut Mungthin, Toon Ruang-areerate, Tawee Naaglor, Picha Suwannahitatorn, Phunlerd Piyaraj, Paanjit Taamasri, Peerapan Tan-ariya, Edoardo Pozio
PLOS Neglected Tropical Diseases.2017; 11(11): e0006030. CrossRef

7,470 View
94 Download
Crossref

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

Abstract
PDF

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

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

8,812 View
109 Download
Crossref

Molecular Detection of Ancylostoma duodenale, Ancylostoma ceylanicum, and Necator americanus in Humans in Northeastern and Southern Thailand: Issarapong Phosuk, Pewpan M. Intapan, Tongjit Thanchomnang, Oranuch Sanpool, Penchom Janwan, Porntip Laummaunwai, Witthaya Aamnart, Nimit Morakote, Wanchai Maleewong; Korean J Parasitol 2013;51(6):747-749.
Published online December 31, 2013; DOI: https://doi.org/10.3347/kjp.2013.51.6.747

Abstract
PDF

The 2 principal species of hookworms infecting humans are Necator americanus and Ancylostoma duodenale. Case studies on zoonotic hookworm infections with Ancylostoma ceylanicum and/or Ancylostoma caninum are known mainly from Asian countries. Of these 2 zoonotic species, only A. ceylanicum can develop to adulthood in humans. In the present study, we report a molecular-based survey of human hookworm infections present in southern and northeastern Thailand. Thirty larval hookworm samples were obtained from fecal agar plate cultures of 10 patients in northeastren Thailand and 20 in southern Thailand. Partial ITS1, 5.8S, and ITS2 regions of the ribosomal DNA genes were amplified using PCR. The amplicons were sequenced, aligned, and compared with other hookworm sequences in GenBank database. The results showed that, in Thailand, N. americanus is more prevalent than Ancylostoma spp. and is found in both study areas. Sporadic cases of A. ceylanicum and A. duodenale infection were seen in northeastern Thailand.

Citations

Citations to this article as recorded by

Efficacy of Simparica Trio® against induced infections of Ancylostoma braziliense and Ancylostoma ceylanicum in dogs
Raj Packianathan, Andrew Hodge, Natalie Bruellke, Michael Pearce, Frans Selepe, Piyanan Taweethavonsawat, Thomas Geurden
Parasites & Vectors.2025;[Epub] CrossRef
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
Development of loop mediated isothermal amplification assay for rapid detection and its comparison with PCR techniques for Ancylostoma duodenale
Mamta Thakur, Abhishek Mewara, P. V. M. Lakshmi, Sucheta Guleria, Sumeeta Khurana
Scientific Reports.2025;[Epub] CrossRef
PERFIL PARASITOLÓGICO DE HORTALIÇAS CULTIVADAS EM HORTAS TRADICIONAIS
Maria Beatriz Neves Nascimento, Monalissa Dias de Souza, Alexandro de Andrade de Lima, Gislaine Cristina de Souza Melanda, Renato Juciano Ferreira
Revista Saúde - UNG-Ser.2025;[Epub] CrossRef
Ancylostoma ceylanicum and other zoonotic canine hookworms: neglected public and animal health risks in the Asia–Pacific region
Jan Clyden B. Tenorio, Ian Kim B. Tabios, Tawin Inpankaew, Adrian P. Ybañez, Saruda Tiwananthagorn, Sirikachorn Tangkawattana, Sutas Suttiprapa
Animal Diseases.2024;[Epub] CrossRef
Molecular identification and genetic diversity of zoonotic hookworm infections in domestic dogs from northeastern, Thailand
Rutchanee Rodpai, Oranuch Sanpool, Lakkhana Sadaow, Patcharaporn Boonroumkaew, Pewpan M. Intapan, Wanchai Maleewong, Manachai Yingklang, Penchom Janwan, Kotchaphon Vaisusuk, Wasupon Chatan, Supawadee Piratae, Tongjit Thanchomnang
Parasitology Research.2024;[Epub] CrossRef
The enhancive effect of the 2014–2016 El Niño-induced drought on the control of soil-transmitted helminthiases without anthelmintics: A longitudinal study
Attarat Pattanawongsa, Pattanasak Kammaneechan, Prasit Na-ek, Blego Sedionoto, Witthaya Anamnart, Qu Cheng
PLOS Neglected Tropical Diseases.2024; 18(7): e0012331. CrossRef
Assessment of an Immuno-Diagnostic Method for Hookworm-Related Cutaneous Larva Migrans Using Crude Extracts of Ancylostoma caninum
Sitthithana Adam, Paron Dekumyoy, Duangporn Nacapunchai, Thawatchai Ketboonlue, Prakaykaew Charunwatthana, Jittima Dhitavat, Khuanchai Koompapong, Putza Chonsawat, Dorn Watthanakulpanich
Tropical Medicine and Infectious Disease.2023; 8(4): 209. CrossRef
Global distribution of human hookworm species and differences in their morbidity effects: a systematic review
Archie C A Clements, Kefyalew Addis Alene
The Lancet Microbe.2022; 3(1): e72. CrossRef
Comparison of percutaneous vs oral infection of hamsters with the hookworm Ancylostoma ceylanicum: Parasite development, pathology and primary immune response
Richard D. Bungiro, Lisa M. Harrison, Blaise Dondji, Michael Cappello, Maria Angeles Gómez-Morales
PLOS Neglected Tropical Diseases.2022; 16(1): e0010098. CrossRef
Prevalence of intestinal parasitic infections and genetic differentiation of Strongyloides stercoralis among migrant workers from Myanmar, Lao PDR and Cambodia in northeastern Thailand
Wararat Sangwalee, Jun Norkaew, Sengchoy Inthachak, Penchom Janwan, Rutchanee Rodpai, Oranuch Sanpool, Lakkhana Sadaow, Patcharaporn Boonroumkaew, Pewpan M. Intapan, Wanchai Maleewong, Tongjit Thanchomnang, Raffi V. Aroian
PLOS ONE.2022; 17(12): e0279754. CrossRef
Copro-molecular identification of intestinal nematode infections in a rural community in East Malaysia
Nur-Amirah Hassan, Autchariya Thodsapol, Yvonne Ai Lian Lim, Wan Yusoff Wan Sulaiman, Siti Farah Norasyikeen Sidi Omar, Kamontam Umsakul, Romano Ngui
Parasitology International.2021; 80: 102237. CrossRef
Soil-transmitted helminths, intestinal protozoa and Clonorchis sinensis infections in southeast China
Yan Feng, Kegen Yu, Hualiang Chen, Xuan Zhang, Qiaoyi Lu, Xiaoxiao Wang, Xueying Zhang, Linong Yao, Wei Ruan
BMC Infectious Diseases.2021;[Epub] CrossRef
Zoonotic hookworms of dogs and cats – lessons from the past to inform current knowledge and future directions of research
Rebecca J. Traub, Patsy A. Zendejas-Heredia, Luca Massetti, Vito Colella
International Journal for Parasitology.2021; 51(13-14): 1233. CrossRef
Molecular identification of hookworm isolates from stray dogs, humans and selected wildlife from South Africa
P. I. Ngcamphalala, J. Lamb, S. Mukaratirwa
Journal of Helminthology.2020;[Epub] CrossRef
Semi-domesticated dogs as a potential reservoir for zoonotic hookworms in Bangkok, Thailand
Jutamas Wongwigkan, Tawin Inpankaew
Veterinary World.2020; 13(5): 909. CrossRef
The increased sensitivity of qPCR in comparison to Kato-Katz is required for the accurate assessment of the prevalence of soil-transmitted helminth infection in settings that have received multiple rounds of mass drug administration
Julia C. Dunn, Marina Papaiakovou, Kay Thwe Han, Darren Chooneea, Alison A. Bettis, Nay Yee Wyine, Aye Moe Moe Lwin, Nay Soe Maung, Raju Misra, D. T. J. Littlewood, Roy M. Anderson
Parasites & Vectors.2020;[Epub] CrossRef
Zoonotic Ancylostomiasis: An Update of a Continually Neglected Zoonosis
Katharina Stracke, Aaron R. Jex, Rebecca J. Traub
The American Journal of Tropical Medicine and Hygiene.2020; 103(1): 64. CrossRef
Of dogs and hookworms: man’s best friend and his parasites as a model for translational biomedical research
Catherine Shepherd, Phurpa Wangchuk, Alex Loukas
Parasites & Vectors.2018;[Epub] CrossRef
Prevalence of Hookworm infection and Strongyloidiasis in Cats and Potential Risk Factor of Human Diseases
Blego Sedionoto, Witthaya Anamnart, Hadiyanto, Sudarno, Maryono
E3S Web of Conferences.2018; 31: 06002. CrossRef
Molecular characterization of hookworm spp. isolated from food handlers, Khartoum, Sudan: A cross-sectional study
Tarig A. Gamar, Hassan H. Musa, Hisham N. Altayb, Mohamed H. Mohamed, Adam D. Abakar
F1000Research.2018; 7: 662. CrossRef
Ancylostoma ceylanicum Hookworm in Myanmar Refugees, Thailand, 2012–2015
Elise M. O’Connell, Tarissa Mitchell, Marina Papaiakovou, Nils Pilotte, Deborah Lee, Michelle Weinberg, Potsawin Sakulrak, Dilok Tongsukh, Georgiette Oduro-Boateng, Sarah Harrison, Steven A. Williams, William M. Stauffer, Thomas B. Nutman
Emerging Infectious Diseases.2018;[Epub] CrossRef
Development and Evaluation of a Multiplex Quantitative Real-Time Polymerase Chain Reaction for Hookworm Species in Human Stool
Sze Fui Hii, Dammika Senevirathna, Stacey Llewellyn, Tawin Inpankaew, Peter Odermatt, Virak Khieu, Sinoun Muth, James McCarthy, Rebecca J. Traub
The American Journal of Tropical Medicine and Hygiene.2018; 99(5): 1186. CrossRef
Hookworm infections among migrant workers in Malaysia: Molecular identification of Necator americanus and Ancylostoma duodenale
Norhidayu Sahimin, Yvonne Ai Lian Lim, Benacer Douadi, Mohd Khairul Nizam Mohd Khalid, John-James Wilson, Jerzy M. Behnke, Siti Nursheena Mohd Zain
Acta Tropica.2017; 173: 109. CrossRef
Prevalence of intestinal parasitic infection and associated risk factors among village health volunteers in rural communities of southern Thailand
Chuchard Punsawad, Nonthapan Phasuk, Suchirat Bunratsami, Kanjana Thongtup, Niramon Siripakonuaong, Somchok Nongnaul
BMC Public Health.2017;[Epub] CrossRef
Soil-Transmitted Helminths in Tropical Australia and Asia
Catherine Gordon, Johanna Kurscheid, Malcolm Jones, Darren Gray, Donald McManus
Tropical Medicine and Infectious Disease.2017; 2(4): 56. CrossRef
Restoration of hookworm egg development after prolonged storage in stool suspension
Prasit Na-Ek, Oranuch Sanpool, Jurairat Jongthawin, Witthaya Anamnart, Pewpan M. Intapan, Pennapa Chamavit, Wanchai Maleewong
Parasitology Research.2016; 115(7): 2817. 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

11,857 View
305 Download
Crossref

Original Article

Susceptibility of Laboratory Rodents to Trichinella papuae: Lakkhana Sadaow, Pewpan M. Intapan, Thidarut Boonmars, Nimit Morakote, Wanchai Maleewong; Korean J Parasitol 2013;51(6):629-632.
Published online December 31, 2013; DOI: https://doi.org/10.3347/kjp.2013.51.6.629

Abstract
PDF

Members of the genus Trichinella are small nematodes that can infect a wide range of animal hosts. However, their infectivity varies depending on the parasite and host species combination. In this study, we examined the susceptibility of 4 species of laboratory rodents, i.e., mice, rats, hamsters, and gerbils to Trichinella papuae, an emerging non-encapsulated Trichinella species. Trichinella spiralis and Trichinella pseudospiralis were also included in this study for comparison. Fifteen animals of each rodent species were infected orally with 100 muscle larvae of each Trichinella species. Intestinal worm burden was determined at day 6 and 10 post-inoculation (PI). The numbers of muscle larvae were examined at day 45 PI. The reproductive capacity index (RCI) of the 3 Trichinella species in different rodent hosts was determined. By day 6 PI, 33.2-69.6% of the inoculated larvae of the 3 Trichinella species became adult worms in the small intestines of the host animals. However, in rats, more than 96% of adult worms of all 3 Trichinella species were expelled from the gut by day 10 PI. In gerbils, only 4.8-18.1% of adult worms were expelled by day 10 PI. In accordance with the intestinal worm burden and the persistence of adults, the RCI was the highest in gerbils with values of 241.5±41.0 for T. papuae, 432.6±48 for T. pseudospiralis, and 528.6±20.6 for T. spiralis. Hamsters ranked second and mice ranked third in susceptibility in terms of the RCI, Rats yielded the lowest parasite RCI for all 3 Trichinella species. Gerbils may be an alternative laboratory animal for isolation and maintenance of Trichinella spp.

Citations

Citations to this article as recorded by

Viability of Trichinella spiralis in traditional sour pork fermentation and its inactivation by microwave heating: Implications for zoonotic risk and food safety
Atchara Artchayasawat, Benjamabhorn Pumhirunroj, Sukhonthip Khueangchiangkhwang, Thidarut Boonmars, Parichart Boueroy, Porntip Laummaunwai, Panaratana Rattanasuwan
Veterinary World.2025; : 1660. CrossRef
Real-time PCR versus traditional and Nano-based ELISA in early detection of murine trichinellosis
S. M. Mohammad, L. A. Hegazy, R. S. Abdel Hady, M. A. Salama, S. K. Hammad, S. M. Ibrahim
Journal of Helminthology.2023;[Epub] CrossRef
A potential herbal therapeutic for trichinellosis
Asmaa M. El-kady, Iman A. M. Abdel-Rahman, Eman Sayed, Majed H. Wakid, Hussah M. Alobaid, Khalil Mohamed, Eman Abdullah Alshehri, Hayam Elshazly, Wafa Abdullah I. Al-Megrin, Furhan Iqbal, Hatem A. Elshabrawy, Ashraf G. Timsah
Frontiers in Veterinary Science.2022;[Epub] CrossRef
Reprint of: Survival of Trichinella spiralis in cured meat products
Annette Johne, Matthias Filter, Jennifer Gayda, Anja Buschulte, Niels Bandick, Karsten Nöckler, Anne Mayer-Scholl
Veterinary Parasitology.2021; 297: 109544. CrossRef
Human Outbreak of Trichinellosis Caused by Trichinella papuae Nematodes, Central Kampong Thom Province, Cambodia
Yannick Caron, Sotharith Bory, Michel Pluot, Mary Nheb, Sarin Chan, Sang Houn Prum, Sun Bun Hong Lim, Mala Sim, Yi Sengdoeurn, Ly Sovann, Virak Khieu, Isabelle Vallée, Hélène Yera
Emerging Infectious Diseases.2020; 26(8): 1759. CrossRef
Survival of Trichinella spiralis in cured meat products
Annette Johne, Matthias Filter, Jennifer Gayda, Anja Buschulte, Niels Bandick, Karsten Nöckler, Anne Mayer-Scholl
Veterinary Parasitology.2020; 287: 109260. CrossRef
Immuno-proteomic analysis of Trichinella spiralis, T. pseudospiralis, and T. papuae extracts recognized by human T. spiralis-infected sera
Chalermchai Somboonpatarakun, Rutchanee Rodpai, Pewpan M. Intapan, Oranuch Sanpool, Lakkhana Sadaow, Chaisiri Wongkham, Tonkla Insawang, Thidarut Boonmars, Wanchai Maleewong
Parasitology Research.2018; 117(1): 201. CrossRef
Differential immune responses in mice infected with the tissue-dwelling nematode Trichinella zimbabwensis
W.N. Onkoba, M.J. Chimbari, J.M. Kamau, S. Mukaratirwa
Journal of Helminthology.2016; 90(5): 547. CrossRef