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

  • HOME
  • BROWSE ARTICLES
  • Previous issues
16
results for

Previous issues

Article category

Keywords

Authors

Previous issues

Prev issue Next issue

Volume 51(4); August 2013

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
  • 20,867 View
  • 340 Download
  • Crossref

Original Articles

Genetic Characterization of Clinical Acanthamoeba Isolates from Japan using Nuclear and Mitochondrial Small Subunit Ribosomal RNA
Md Moshiur Rahman, Kenji Yagita, Akira Kobayashi, Yosaburo Oikawa, Amjad I.A. Hussein, Takahiro Matsumura, Masaharu Tokoro
Korean J Parasitol 2013;51(4):401-411.
Published online August 30, 2013
DOI: https://doi.org/10.3347/kjp.2013.51.4.401

Because of an increased number of Acanthamoeba keratitis (AK) along with associated disease burdens, medical professionals have become more aware of this pathogen in recent years. In this study, by analyzing both the nuclear 18S small subunit ribosomal RNA (18S rRNA) and mitochondrial 16S rRNA gene loci, 27 clinical Acanthamoeba strains that caused AK in Japan were classified into 3 genotypes, T3 (3 strains), T4 (23 strains), and T5 (one strain). Most haplotypes were identical to the reference haplotypes reported from all over the world, and thus no specificity of the haplotype distribution in Japan was found. The T4 sub-genotype analysis using the 16S rRNA gene locus also revealed a clear sub-conformation within the T4 cluster, and lead to the recognition of a new sub-genotype T4i, in addition to the previously reported sub-genotypes T4a-T4h. Furthermore, 9 out of 23 strains in the T4 genotype were identified to a specific haplotype (AF479533), which seems to be a causal haplotype of AK. While heterozygous nuclear haplotypes were observed from 2 strains, the mitochondrial haplotypes were homozygous as T4 genotype in the both strains, and suggested a possibility of nuclear hybridization (mating reproduction) between different strains in Acanthamoeba. The nuclear 18S rRNA gene and mitochondrial 16S rRNA gene loci of Acanthamoeba spp. possess different unique characteristics usable for the genotyping analyses, and those specific features could contribute to the establishment of molecular taxonomy for the species complex of Acanthamoeba.

Citations

Citations to this article as recorded by  Crossref logo
  • Molecular Evidence for Greater Diversity Within Acanthamoeba
    Daniele Corsaro
    Acta Parasitologica.2025;[Epub]     CrossRef
  • Molecular Typing of Acanthamoeba Using Mitochondrial rDNA Spacers
    Daniele Corsaro
    Microorganisms.2025; 13(10): 2285.     CrossRef
  • Sub-Genotyping of Acanthamoeba T4 Complex: Experience from North India
    Kirti Megha, Megha Sharma, Amit Gupta, Rakesh Sehgal, Sumeeta Khurana
    Parasitologia.2023; 3(1): 69.     CrossRef
  • Molecular evidence for a new lineage within the Acanthamoeba T4 genotype
    Daniele Corsaro, Danielle Venditti
    Parasitology Research.2023; 122(6): 1445.     CrossRef
  • Identification and genotyping of Acanthamoeba spp. in the water resources of western Iran
    Azadeh Karimi, Farnaz Kheirandish, Amirreza Javadi Mamaghani, Niloofar Taghipour, Syedeh Fatemeh Mousavi, Ali Aghajani, Nozhat Zebardast, Majid Faraji, Shirzad Fallahi
    Parasite Epidemiology and Control.2023; 22: e00308.     CrossRef
  • The Risk Factors and Clinical Features of Acanthamoeba Keratitis: First Time Detection of Acanthamoeba T5 Genotype from Keratitis Patients in Turkey
    Derya Dirim Erdogan, Mehmet Aykur, Nur Selvi Gunel, Melis Palamar, Ozlem Barut Selver, Buket Ozel, Ayse Yagci, Cumhur Gunduz, Hande Dagci
    Acta Parasitologica.2022; 67(3): 1384.     CrossRef
  • Exploring LSU and ITS rDNA Sequences for Acanthamoeba Identification and Phylogeny
    Daniele Corsaro
    Microorganisms.2022; 10(9): 1776.     CrossRef
  • Genotype distribution of Acanthamoeba in keratitis: a systematic review
    Maria Luisa Nunes Diehl, Júlia Paes, Marilise Brittes Rott
    Parasitology Research.2021; 120(9): 3051.     CrossRef
  • Molecular identification and phylogenetic analysis of free-living amoeba (Naegleria and Acanthamoeba) from treated and untreated drinking water
    Omid Ahmadi, Yousef Sharifi, Nazgol Khosravinia, Elham Moghaddas, Mohammad Akhoundi, Reza Fotouhi-Ardakani, Jaber Asadi, Amir Hossein Mohamadzade, Ghodratolah Salehi Sangani, Hamed Mirjalali, Mehdi Zarean
    Gene Reports.2021; 25: 101328.     CrossRef
  • Isolates from ancient permafrost help to elucidate species boundaries in Acanthamoeba castellanii complex (Amoebozoa: Discosea)
    Stas Malavin, Lyubov Shmakova
    European Journal of Protistology.2020; 73: 125671.     CrossRef
  • Update on Acanthamoeba phylogeny
    Daniele Corsaro
    Parasitology Research.2020; 119(10): 3327.     CrossRef
  • Lower prevalence of Entamoeba species in children with vertically transmitted HIV infection in Western Kenya
    Elizabeth Jemaiyo Matey, Masaharu Tokoro, Takehiro Nagamoto, Tetsushi Mizuno, Matilda Chelimo Saina, Xiuqiong Bi, Jane A. Oyombra, Paul Okumu, Benard Kibet Langat, Willie Kipkemboi Sang, Elijah Maritim Songok, Hiroshi Ichimura
    AIDS.2016; 30(5): 803.     CrossRef
  • Positive correlation of HIV infection with Giardia intestinalis assemblage B but not with assemblage A in asymptomatic Kenyan children
    Elizabeth J. Matey, Masaharu Tokoro, Tetsushi Mizuno, Takahiro Matsumura, Takehiro Nagamoto, Xiuqiong Bi, Jane A. Oyombra, Willie K. Sang, Elijah M. Songok, Hiroshi Ichimura
    AIDS.2016; 30(15): 2385.     CrossRef
  • Isolation and Genotyping of Acanthamoeba spp. as Neglected Parasites in North of Iran
    Azar Shokri, Shahabeddin Sarvi, Ahmad Daryani, Mehdi Sharif
    The Korean Journal of Parasitology.2016; 54(4): 447.     CrossRef
  • Presence of potential pathogenic genotypes of free-living amoebae isolated from sandboxes in children's playgrounds
    Marcin Cholewinski, Piotr Solarczyk, Monika Derda, Agnieszka Wojtkowiak-Giera, Edward Hadas
    Folia Parasitologica.2015;[Epub]     CrossRef
  • Morphological Features andIn VitroCytopathic Effect ofAcanthamoeba griffiniTrophozoites Isolated from a Clinical Case
    Arturo González-Robles, Lizbeth Salazar-Villatoro, Maritza Omaña-Molina, Maria Reyes-Batlle, Carmen M. Martín-Navarro, Jacob Lorenzo-Morales
    Journal of Parasitology Research.2014; 2014: 1.     CrossRef
  • 11,594 View
  • 116 Download
  • Crossref
Overexpression of Ubiquitin and Amino Acid Permease Genes in Association with Antimony Resistance in Leishmania tropica Field Isolates
Elham Kazemi-Rad, Mehdi Mohebali, Mohammad Bagher Khadem-Erfan, Homa Hajjaran, Ramtin Hadighi, Ali Khamesipour, Sassan Rezaie, Mojtaba Saffari, Reza Raoofian, Mansour Heidari
Korean J Parasitol 2013;51(4):413-419.
Published online August 30, 2013
DOI: https://doi.org/10.3347/kjp.2013.51.4.413

The mainstay therapy against leishmaniasis is still pentavalent antimonial drugs; however, the rate of antimony resistance is increasing in endemic regions such as Iran. Understanding the molecular basis of resistance to antimonials could be helpful to improve treatment strategies. This study aimed to recognize genes involved in antimony resistance of Leishmania tropica field isolates. Sensitive and resistant L. tropica parasites were isolated from anthroponotic cutaneous leishmaniasis patients and drug susceptibility of parasites to meglumine antimoniate (Glucantime®) was confirmed using in vitro assay. Then, complementary DNA-amplified fragment length polymorphism (cDNA-AFLP) and real-time reverse transcriptase-PCR (RT-PCR) approaches were utilized on mRNAs from resistant and sensitive L. tropica isolates. We identified 2 known genes, ubiquitin implicated in protein degradation and amino acid permease (AAP3) involved in arginine uptake. Also, we identified 1 gene encoding hypothetical protein. Real-time RT-PCR revealed a significant upregulation of ubiquitin (2.54-fold), and AAP3 (2.86-fold) (P<0.05) in a resistant isolate compared to a sensitive one. Our results suggest that overexpression of ubiquitin and AAP3 could potentially implicated in natural antimony resistance.

Citations

Citations to this article as recorded by  Crossref logo
  • Comparative transcriptomics of naturally susceptible and resistant Trypanosoma cruzi strains in response to Benznidazole
    Carlos Ospina, Tatiana Cáceres, Stivenn Gutiérrez, Luz Helena Patiño, Luis David Sáenz-Pérez, Karen Moreno Medina, Juan Carlos Villar, Juan David Ramírez
    International Journal for Parasitology: Drugs and Drug Resistance.2025; 29: 100623.     CrossRef
  • Leishmania spp. genetic factors associated with cutaneous leishmaniasis antimony pentavalent drug resistance: a systematic review
    Raphaela Lisboa Andrade Nery, Thaline Mabel Sousa Santos, Luana Leandro Gois, Aldina Barral, Ricardo Khouri, Caroline Alves Feitosa, Luciane Amorim Santos
    Memórias do Instituto Oswaldo Cruz.2024;[Epub]     CrossRef
  • Transcriptomic analysis of benznidazole-resistant and susceptible Trypanosoma cruzi populations
    Davi Alvarenga Lima, Leilane Oliveira Gonçalves, João Luís Reis-Cunha, Paul Anderson Souza Guimarães, Jeronimo Conceição Ruiz, Daniel Barbosa Liarte, Silvane Maria Fonseca Murta
    Parasites & Vectors.2023;[Epub]     CrossRef
  • Quantitative proteomic analysis reveals differential modulation of crucial stage specific proteins during promastigote to amastigote differentiation in Leishmania donovani
    Chinmayee Bar Routaray, Vaibhavee Choudhari, Divya Prakash, Rajendra Patil, Surabhi Jagtap, Shakuntala Bai, Mahesh J. Kulkarni, Suresh V. Kuchipudi, Kalpana Pai
    Journal of Proteins and Proteomics.2022; 13(1): 17.     CrossRef
  • Leishmania infantum UBC1 in Metacyclic Promastigotes from Phlebotomus perniciosus, a Vaccine Candidate for Zoonotic Visceral Leishmaniasis
    Jaime Larraga, Pedro Alcolea, Ana Alonso, Luis Martins, Inmaculada Moreno, Mercedes Domínguez, Vicente Larraga
    Vaccines.2022; 10(2): 231.     CrossRef
  • Global distribution of treatment resistance gene markers for leishmaniasis
    Samira Salari, Mehdi Bamorovat, Iraj Sharifi, Pooya Ghasemi Nejad Almani
    Journal of Clinical Laboratory Analysis.2022;[Epub]     CrossRef
  • Elucidation of the Flavor Aspects and Flavor-Associated Genomic Regions in Bottle Gourd (Lagenaria siceraria) by Metabolomic Analysis and QTL-seq
    Ying Wang, Yanwei Li, Xiaohua Wu, Xinyi Wu, Zishan Feng, Jian Wang, Baogen Wang, Zhongfu Lu, Guojing Li
    Foods.2022; 11(16): 2450.     CrossRef
  • Effect of the variation in the extracellular concentration of l-arginine in the physiology of Leishmania (Viannia) braziliensis and its susceptibility to some antileishmanial drugs
    Manuela Giraldo, Yulieth A. Upegui, Jorge L. Higuita-Castro, Luis A. Gonzalez, Sneider Gutierrez, Sergio A. Pulido, Sara M. Robledo
    Experimental Parasitology.2022; 242: 108395.     CrossRef
  • HAS 1: A natural product from soil-isolated Streptomyces species with potent activity against cutaneous leishmaniasis caused by Leishmania tropica
    Bassel Awada, Maguy Hamie, Rana El Hajj, Ghada Derbaj, Rania Najm, Perla Makhoul, Dima Hajj Ali, Antoine G. Abou Fayad, Hiba El Hajj
    Frontiers in Pharmacology.2022;[Epub]     CrossRef
  • Metabolite Biomarkers of Leishmania Antimony Resistance
    Sneider Alexander Gutierrez Guarnizo, Zemfira N. Karamysheva, Elkin Galeano, Carlos E. Muskus
    Cells.2021; 10(5): 1063.     CrossRef
  • Voriconazole resistance genes in Aspergillus flavus clinical isolates
    F. Zaini, E. Lotfali, A. Fattahi, E. Siddig, S. Farahyar, E. Kouhsari, M. Saffari
    Journal de Mycologie Médicale.2020; 30(2): 100953.     CrossRef
  • Comparative transcriptomic analysis of antimony resistant and susceptible Leishmania infantum lines
    Juvana Moreira Andrade, Leilane Oliveira Gonçalves, Daniel Barbosa Liarte, Davi Alvarenga Lima, Frederico Gonçalves Guimarães, Daniela de Melo Resende, Ana Maria Murta Santi, Luciana Marcia de Oliveira, João Paulo Linhares Velloso, Renato Guimarães Delfin
    Parasites & Vectors.2020;[Epub]     CrossRef
  • An overview of leishmanization experience: A successful control measure and a tool to evaluate candidate vaccines
    Mehdi Mohebali, Abolhassan Nadim, Ali Khamesipour
    Acta Tropica.2019; 200: 105173.     CrossRef
  • Comparison of Cysteine Protease B Gene Expression between Clinical Isolates of Leishmania tropica, Leishmania major and Leishmania infantum
    Elham Kazemirad, Hossien Reisi Nafchi, Alireza Latifi, Reza Raoofian, Mehdi Mohebali, Homa Hajjaran
    Journal of Medical Microbiology and Infectious Diseases.2019; 7(3): 72.     CrossRef
  • Use of AFLP for the study of eukaryotic pathogens affecting humans
    Carlos M. Restrepo, Alejandro Llanes, Ricardo Lleonart
    Infection, Genetics and Evolution.2018; 63: 360.     CrossRef
  • Expression analysis of viscerotropic leishmaniasis gene in Leishmania species by real-time RT-PCR
    Hossein Reisi Nafchi, Elham Kazemi-Rad, Mehdi Mohebali, Reza Raoofian, Niloofar Bavarsad Ahmadpour, Mohammad Ali Oshaghi, Homa Hajjaran
    Acta Parasitologica.2016;[Epub]     CrossRef
  • Expression analysis of activated protein kinase C gene (LACK1) in antimony sensitive and resistant Leishmania tropica clinical isolates using real‐time RT‐PCR
    Homa Hajjaran, Elham Kazemi‐Rad, Mehdi Mohebali, Mohammad A. Oshaghi, Mohammad B. Khadem‐Erfan, Elham Hajaliloo, Hossein Reisi Nafchi, Reza Raoofian
    International Journal of Dermatology.2016; 55(9): 1020.     CrossRef
  • Visceral Leishmaniasis without Fever in an 11-Month-Old Infant: a Rare Clinical Feature of Kala-azar
    Shirin Sayyahfar, Shahla Ansari, Mehdi Mohebali, Babak Behnam
    The Korean Journal of Parasitology.2014; 52(2): 189.     CrossRef
  • 8,994 View
  • 90 Download
  • Crossref
Influence of Toxoplasma gondii Acute Infection on Cholinesterase Activities of Wistar Rats
Alexandre Alberto Tonin, Aleksandro Schafer da Silva, Maria Luiza Thorstenberg, L?via Gelain Castilhos, Raqueli Teresinha Fran?a, Daniela Bitencourt Rosa Leal, Marta Maria Medeiros Frescura Duarte, Fernanda Silveira Flores Vogel, Mario Luiz de La Rue, Sonia Terezinha dos Anjos Lopes
Korean J Parasitol 2013;51(4):421-426.
Published online August 30, 2013
DOI: https://doi.org/10.3347/kjp.2013.51.4.421

Several studies have shown the mechanisms and importance of immune responses against Toxoplasma gondii infection and the notable role of cholinesterases in inflammatory reactions. However, the association between those factors has not yet been investigated. Therefore, the aim of this study was to evaluate the acetylcholinesterase (AChE) activity in blood and lymphocytes and the activity of butyrylcholinesterase (BChE) in serum of rats experimentally infected with T. gondii during the acute phase of infection. For that, an in vivo study was performed with evaluations of AChE and BChE activities on days 5 and 10 post-infection (PI). The activity of AChE in blood was increased on day 5 PI, while in lymphocytes its activity was enhanced on days 5 and 10 PI (P<0.05). No significant difference was observed between groups regarding to the activity of BChE in serum. A positive (P<0.01) correlation was observed between AChE activity and number of lymphocytes. The role of AChE as an inflammatory marker is well known in different pathologies; thus, our results lead to the hypothesis that AChE has an important role in modulation of early immune responses against T. gondii infection.

Citations

Citations to this article as recorded by  Crossref logo
  • A meta-analysis of changes in cholinesterase activity among experimental animals infected with Toxoplasma gondii
    F. K. Mohammad, S. H. Eassa, R. G. Abdullah
    BULGARIAN JOURNAL OF VETERINARY MEDICINE.2025; 28(2): 195.     CrossRef
  • Variation in Gene Expression Across Infection Status and Elevation in a Hawaiian Honeycreeper
    Loren Cassin‐Sackett, Katherine M. McClure, Taylor E. Callicrate, Eben H. Paxton, Robert C. Fleischer
    Ecology and Evolution.2025;[Epub]     CrossRef
  • Plasma Cholinesterase Activity in Patients With Rheumatoid Arthritis and Toxoplasmosis
    Rabie G Abdullah, Souzan H Eassa, Fouad K Mohammad
    Cureus.2023;[Epub]     CrossRef
  • Toxoplasmosis: Targeting neurotransmitter systems in psychiatric disorders
    Tooran Nayeri, Shahabeddin Sarvi, Ahmad Daryani
    Metabolic Brain Disease.2022; 37(1): 123.     CrossRef
  • Toxoplasma gondii: A possible etiologic agent for Alzheimer's disease
    Tooran Nayeri, Shahabeddin Sarvi, Mehdi Sharif, Ahmad Daryani
    Heliyon.2021; 7(6): e07151.     CrossRef
  • Diagnostic significance of C-reactive protein and hematological parameters in acute toxoplasmosis
    Vanessa Sandri, Itamar Luís Gonçalves, Gustavo Machado das Neves, Marisa Lucia Romani Paraboni
    Journal of Parasitic Diseases.2020; 44(4): 785.     CrossRef
  • STUDY ON THE PREVALENCE AND HEMATOLOGICAL ALTERATIONS IN TOXOPLASMA GONDII INFECTED CAPTIVE PHEASANT SPECIES OF BAHAWALPUR ZOO, PAKISTAN
    M.H. Lashari, M Bibi, U Farooq, F Afzal, A Ali, M Safdar, M.S. Akhtar, A.A. Farooq, S Masood, M Ayaz, M.I. Khan
    The Journal of Animal and Plant Sciences.2020; 31(2): 625.     CrossRef
  • Is There a Cholinergic Survival Incentive for Neurotropic Parasites in the Brain?
    Abdul Mannan Baig
    ACS Chemical Neuroscience.2017; 8(12): 2574.     CrossRef
  • Sulfamethoxazole-trimethoprim associated with resveratrol for the treatment of toxoplasmosis in mice: Influence on the activity of enzymes involved in brain neurotransmission
    Nathieli B. Bottari, Matheus D. Baldissera, Alexandre A. Tonin, Virginia C. Rech, Vivian S.K. Nishihira, Gustavo R. Thomé, Maria Rosa C. Schetinger, Vera M. Morsch, Giovana Camillo, Fernanda F. Vogel, Camila Tochetto, Rafael Fighera, Gustavo Machado, Leni
    Microbial Pathogenesis.2015; 79: 17.     CrossRef
  • 8,772 View
  • 70 Download
  • Crossref

A new trichostome ciliate, Balantidium honghuensis n. sp., was isolated from the recta of Rana nigromaculata and R. limnocharis during parasite surveys in Honghu Lake, Hubei Province, central China in summer of 2010 and 2011. Its detailed morphometric characters based on LM and SEM studies were described herein. The organism is oval in shape and thickly ciliated. The vestibulum is "V" shaped and occupies about 1/3 to 2/5 of the body length. The vestibular and nearby regions possess strong peripheral fibers which form a marked axial fiber about the cytopharynx. More than 10 contractile vacuoles are distributed along the periphery of the latter body. Comparisions were made between this new species and B. sinensis Nie, 1935. They were discriminated from each other in terms of general body forms, body size, and vestibulum shapes. Besides, special attention was paid to its high-speed daughter swarmers which we believed to be the infective stage of B. honghuensis. Possible infection routes of anura amphibian balantidia were discussed.

Citations

Citations to this article as recorded by  Crossref logo
  • Gastrointestinal parasites in bullfrogs (Lithobates catesbeianus) in aquaculture production units in the Mexican central highlands
    Emmanuel Hernández-Valdivia, Efraín Islas-Ojeda, Rafael Casillas-Peñuelas, Arturo Valdivia-Flores, Alberto García-Munguía
    Revista Brasileira de Parasitologia Veterinária.2023;[Epub]     CrossRef
  • The energy metabolism of Balantidium polyvacuolum inhabiting the hindgut of Xenocypris davidi
    Xia-lian Bu, Wei-shan Zhao, Zhong-yang Li, Hong-wei Ma, Yu-shun Chen, Wen-xiang Li, Hong Zou, Ming Li, Gui-tang Wang
    BMC Genomics.2023;[Epub]     CrossRef
  • Balantidium grimi n. sp. (Ciliophora, Litostomatea), a new species inhabiting the rectum of the frog Quasipaa spinosa from Lishui, China
    Weishan Zhao, Can Li, Dong Zhang, Runqiu Wang, Yingzhen Zheng, Hong Zou, Wenxiang Li, Shangong Wu, Guitang Wang, Ming Li
    Parasite.2018; 25: 29.     CrossRef
  • Phylogenomic analysis ofBalantidium ctenopharyngodoni(Ciliophora, Litostomatea) based on single-cell transcriptome sequencing
    Zongyi Sun, Chuanqi Jiang, Jinmei Feng, Wentao Yang, Ming Li, Wei Miao
    Parasite.2017; 24: 43.     CrossRef
  • Reisolation and redescription of Balantidium duodeni Stein, 1867 (Litostomatea, Trichostomatia)
    Lyudmila V. Chistyakova, Alexei Yu. Kostygov, Olga A. Kornilova, Vyacheslav Yurchenko
    Parasitology Research.2014; 113(11): 4207.     CrossRef
  • New insights into the molecular phylogeny of Balantidium (Ciliophora, Vetibuliferida) based on the analysis of new sequences of species from fish hosts
    Ming Li, Francisco Ponce-Gordo, J. Norman Grim, Chong Wang, Frank Nilsen
    Parasitology Research.2014; 113(12): 4327.     CrossRef
  • 10,229 View
  • 106 Download
  • Crossref
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
  • 12,729 View
  • 163 Download
  • Crossref
First Record of Bourgelatia diducta (Nematoda: Chabertiidae) from Wild Boars in the Republic of Korea
Kyu-Sung Ahn, Dae-Sung Oh, Ah-Jin Ahn, Guk-Hyun Suh, Sung-Shik Shin
Korean J Parasitol 2013;51(4):441-448.
Published online August 30, 2013
DOI: https://doi.org/10.3347/kjp.2013.51.4.441

This study describes the first record of Bourgelatia diducta (Nematoda: Chabertiidae) from wild boars in the Republic of Korea (=South Korea). Gastrointestinal tracts of 87 Korean wild boars (Sus scrofa coreanus) hunted in mountains in the south-western part of South Korea between 2009 and 2012 were examined for their visceral helminths. B. diducta, as identified by morphological characteristics of the head and tail, were recovered from the large intestine of 47 (54%) wild boars. The average length of adult female worms was 11.3±0.87 mm and the thickest part of the body measured 0.54±0.04 mm in maximum width, while those of males were 9.8±0.72 and 0.45±0.03 mm, respectively. The characteristic J-shaped type II ovejector was observed in females, and the type II dorsal ray with 2 rami on each side of the median fissure was uniquely seen in males. The buccal capsule was small, relatively thin-walled, cylindrical, very short, and ring-shaped. The externodorsal ray arose from a common stem with the dorsal ray. The cervical groove was absent. The anterior extremity was equipped with 20-22 external corona radiata, 4 cephalic papillae and 2 lateral amphids around the mouth. The eggs were 66.0×38.9 ?m in average size. By the present study, B. diducta (Nematoda: Chabertiidae) is recorded for the first time in South Korea. Additionally, morphological characteristics and identification keys provided in the present study will be helpful in the faunistic or taxonomic studies for strongylid nematodes related.

Citations

Citations to this article as recorded by  Crossref logo
  • Identification and Prevalence of Globocephalus samoensis (Nematoda: Ancylostomatidae) among Wild Boars (Sus scrofa coreanus) from Southwestern Regions of Korea
    Kyu-Sung Ahn, Ah-Jin Ahn, Tae-Hoon Kim, Guk-Hyun Suh, Kyoung-Woong Joo, Sung-Shik Shin
    The Korean Journal of Parasitology.2015; 53(5): 611.     CrossRef
  • 10,611 View
  • 121 Download
  • Crossref
Genetic Variation of Taenia Pisiformis Collected from Sichuan, China, Based on the Mitochondrial Cytochrome b gene
Deying Yang, Yongjun Ren, Yan Fu, Yue Xie, Huaming Nie, Xiang Nong, Xiaobin Gu, Shuxian Wang, Xuerong Peng, Guangyou Yang
Korean J Parasitol 2013;51(4):449-452.
Published online August 30, 2013
DOI: https://doi.org/10.3347/kjp.2013.51.4.449

Taenia pisiformis is one of the most important parasites of canines and rabbits. T. pisiformis cysticercus (the larval stage) causes severe damage to rabbit breeding, which results in huge economic losses. In this study, the genetic variation of T. pisiformis was determined in Sichuan Province, China. Fragments of the mitochondrial cytochrome b (cytb) (922 bp) gene were amplified in 53 isolates from 8 regions of T. pisiformis. Overall, 12 haplotypes were found in these 53 cytb sequences. Molecular genetic variations showed 98.4% genetic variation derived from intra-region. FST and Nm values suggested that 53 isolates were not genetically differentiated and had low levels of genetic diversity. Neutrality indices of the cytb sequences showed the evolution of T. pisiformis followed a neutral mode. Phylogenetic analysis revealed no correlation between phylogeny and geographic distribution. These findings indicate that 53 isolates of T. pisiformis keep a low genetic variation, which provide useful knowledge for monitoring changes in parasite populations for future control strategies.

Citations

Citations to this article as recorded by  Crossref logo
  • Sequence analysis of the cytb gene of Mesocestoides Vaillant, 1863 tetrathyridia from small mammals of the Russian Far East
    N.A. Pospekhova, V.V. Pereverzeva, N.E. Dokuchaev, A.A. Primak
    Proceedings of the Zoological Institute RAS.2025; 329(1): 64.     CrossRef
  • A survey of morphological, molecular, and histopathological characteristics of Taenia pisiformis metacestode in Egyptian rabbits (Oryctolagus cuniculus)
    Refaat Ras, Amanallah El-Bahrawy, Adel Abdelkhalek, Florica Morariu, Ayman N. Elsayed, Doaa S. Nouh, Anamaria Plesko, Marius Stelian Ilie, Manar AbdelMageed
    Frontiers in Veterinary Science.2025;[Epub]     CrossRef
  • Infection of Egyptian domestic rabbits, Oryctolagus cuniculus, with Cysticercus pisiformis (Cestoda: Taeniidae): morphological, molecular, and histopathological diagnostic tools
    Soheir A. H. Rabie, Wafaa A. Abuelwafa, Mouchira M. Mohi Eldin, Nermean M. Hussein
    Journal of Parasitic Diseases.2024; 48(4): 810.     CrossRef
  • Morphometry, molecular identification and histopathology of Passalurus ambiguus Rudolphi, 1819 in domestic rabbits (Oryctolagus cuniculus) in Qena, Upper Egypt
    Nermean M. Hussein, Soheir A. H. Rabie, Wafaa A. Abuelwafa, Mouchira M. Mohi ElDin
    Journal of Parasitic Diseases.2022; 46(2): 511.     CrossRef
  • Theileria, Hepatozoon and Taenia infection in great gerbils (Rhombomys opimus) in northwestern China
    Na Ji, Xueling Chen, Gang Liu, Shanshan Zhao, Wenbo Tan, Guangyuan Liu, Jiangguo Zhang, Yuanzhi Wang
    International Journal for Parasitology: Parasites and Wildlife.2021; 15: 79.     CrossRef
  • Molecular Confirmation of Massive Taenia pisiformis Cysticercosis in One Rabbit in Poland
    Małgorzata Samorek-Pieróg, Jacek Karamon, Adam Brzana, Ewa Bilska-Zając, Jolanta Zdybel, Tomasz Cencek
    Pathogens.2021; 10(8): 1029.     CrossRef
  • Spatiotemporal monitoring of Cysticercus pisiformis in European wild rabbit (Oryctolagus cuniculus) in Mediterranean ecosystems in southern Spain
    Susana Remesar, Sabrina Castro-Scholten, Débora Jiménez-Martín, Leonor Camacho-Sillero, Patrocinio Morrondo, Carlos Rouco, Félix Gómez-Guillamón, David Cano-Terriza, Ignacio García-Bocanegra
    Preventive Veterinary Medicine.2021; 197: 105508.     CrossRef
  • Molecular Characterization of Enterocytozoon bieneusi in Domestic Rabbits (Oryctolagus cuniculus) in Northeastern China
    Xiao-Xuan Zhang, Jing Jiang, Ya-Nan Cai, Chun-Feng Wang, Peng Xu, Gui-Lian Yang, Quan Zhao
    The Korean Journal of Parasitology.2016; 54(1): 81.     CrossRef
  • Genetic Structure Analysis of Spirometra erinaceieuropaei Isolates from Central and Southern China
    Xi Zhang, Jing Cui, Li Na Liu, Peng Jiang, Han Wang, Xin Qi, Xing Qi Wu, Zhong Quan Wang, Wolfgang Arthofer
    PLOS ONE.2015; 10(3): e0119295.     CrossRef
  • 9,681 View
  • 92 Download
  • Crossref
Skeletal Manifestations of Hydatid Disease in Serbia: Demographic Distribution, Site Involvement, Radiological Findings, and Complications
Djurdja Bracanovic, Marija Djuric, Jelena Sopta, Danijela Djonic, Nenad Lujic
Korean J Parasitol 2013;51(4):453-459.
Published online August 30, 2013
DOI: https://doi.org/10.3347/kjp.2013.51.4.453

Although Serbia is recognized as an endemic country for echinococcosis, no information about precise incidence in humans has been available. The aim of this study was to investigate the skeletal manifestations of hydatid disease in Serbia. This retrospective study was conducted by reviewing the medical database of Institute for Pathology (Faculty of Medicine in Belgrade), a reference institution for bone pathology in Serbia. We reported a total of 41 patients with bone cystic echinococcosis (CE) during the study period. The mean age of 41 patients was 40.9±18.8 years. In 39% of patients, the fracture line was the only visible radiological sign, followed by cyst and tumefaction. The spine was the most commonly involved skeletal site (55.8%), followed by the femur (18.6%), pelvis (13.9%), humerus (7.0%), rib (2.3%), and tibia (2.3%). Pain was the symptom in 41.5% of patients, while some patients demonstrated complications such as paraplegia (22.0%), pathologic fracture (48.8%), and scoliosis (9.8%). The pathological fracture most frequently affected the spine (75.0%) followed by the femur (20.0%) and tibia (5.0%). However, 19.5% of patients didn't develop any complication or symptom. In this study, we showed that bone CE is not uncommon in Serbian population. As reported in the literature, therapy of bone CE is controversial and its results are poor. In order to improve the therapy outcome, early diagnosis, before symptoms and complications occur, can be contributive.

Citations

Citations to this article as recorded by  Crossref logo
  • Vertebral and pelvic echinococcosis in northwestern China
    Laihong Yang, Pahati Tuxunjiang, Wenya Liu, Hui Guo
    International Orthopaedics.2023; 47(5): 1153.     CrossRef
  • Complete excision of giant clavicular hydatid cyst: a case report
    Xin Wang, Jinyong Huang, Liping Su, Qian Ma, Chao Ma, Zengru Xie
    BMC Infectious Diseases.2023;[Epub]     CrossRef
  • Hydatid disease of bone
    Hui Guo, Pahati Tuxunjiang, Laihong Yang, Wenya Liu
    Radiology of Infectious Diseases.2022; 9(1): 18.     CrossRef
  • Cystic Echinococcosis of the Bone: A European Multicenter Study
    Letizia Cattaneo, Tommaso Manciulli, Carmen-Michaela Cretu, Maria Teresa Giordani, Andrea Angheben, Alessandro Bartoloni, Lorenzo Zammarchi, Filippo Bartalesi, Joachim Richter, Peter Chiodini, Gauri Godbole, Thomas Junghanss, Marija Stojkovic, Luigi Samma
    The American Journal of Tropical Medicine and Hygiene.2019; 100(3): 617.     CrossRef
  • Human hydatid disease and its effect on bones and joints: edital
    MA Gracio
    MOJ Public Health.2019; 8(4): 121.     CrossRef
  • Cystic Echinococcosis of the Bone in Kazakhstan
    Tommaso Manciulli, Aigerim Mustapayeva, Konrad Juszkiewicz, Ekaterina Sokolenko, Zhaksylik Maulenov, Ambra Vola, Mara Mariconti, Gani Serikbaev, Amangul Duisenova, Enrico Brunetti, Zhamilya Zholdybay
    Case Reports in Infectious Diseases.2018; 2018: 1.     CrossRef
  • Fractures de côtes non traumatiques
    Yves Maugars, Marguerite Mary-Chemel, Christelle Laffite-Darrieutort, Pascale Guillot, Joëlle Glémarec, Jean-Marie Berthelot, Benoit Le Goff
    Revue du Rhumatisme Monographies.2015; 82(2): 109.     CrossRef
  • Giant hydatid cyst of the pelvis, femur and retroperitoneal space: surgical treatment with extended hemipelvectomy
    Panagiotis Tsagozis, Otte Brosjö
    BMJ Case Reports.2015; 2015: bcr2015209715.     CrossRef
  • Reports of four cyst hydatid cases in different size and location
    Elif Tukenmez Tigen, Buket Erturk Sengel, Huseyin Bilgin, Serra Ozel, Lutfiye Mulazimoglu
    Asian Pacific Journal of Tropical Disease.2014; 4(5): 408.     CrossRef
  • Bone cyst: Case report and implications for the anaesthesiologist
    Chhavi Sawhney, Ghansham Biyani, Sadik Mohammed, Pallavi Shende
    Indian Journal of Anaesthesia.2014; 58(6): 767.     CrossRef
  • 10,149 View
  • 96 Download
  • Crossref

Case Reports

A Waterborne Outbreak and Detection of Cryptosporidium Oocysts in Drinking Water of an Older High-Rise Apartment Complex in Seoul
Eun-Joo Cho, Jin-Young Yang, Eun-Sook Lee, Se-Chul Kim, So-Yang Cha, Sung-Tek Kim, Man-Ho Lee, Sun-Hee Han, Young-Sang Park
Korean J Parasitol 2013;51(4):461-466.
Published online August 30, 2013
DOI: https://doi.org/10.3347/kjp.2013.51.4.461

From May to June 2012, a waterborne outbreak of 124 cases of cryptosporidiosis occurred in the plumbing systems of an older high-rise apartment complex in Seoul, Republic of Korea. The residents of this apartment complex had symptoms of watery diarrhea and vomiting. Tap water samples in the apartment complex and its adjacent buildings were collected and tested for 57 parameters under the Korean Drinking Water Standards and for additional 11 microbiological parameters. The microbiological parameters included total colony counts, Clostridium perfringens, Enterococcus, fecal streptococcus, Salmonella, Shigella, Pseudomonas aeruginosa, Cryptosporidium oocysts, Giardia cysts, total culturable viruses, and Norovirus. While the tap water samples of the adjacent buildings complied with the Korean Drinking Water Standards for all parameters, fecal bacteria and Cryptosporidium oocysts were detected in the tap water samples of the outbreak apartment complex. It turned out that the agent of the disease was Cryptosporidium parvum. The drinking water was polluted with sewage from a septic tank in the apartment complex. To remove C. parvum oocysts, we conducted physical processes of cleaning the water storage tanks, flushing the indoor pipes, and replacing old pipes with new ones. Finally we restored the clean drinking water to the apartment complex after identification of no oocysts.

Citations

Citations to this article as recorded by  Crossref logo
  • Disruptive effects of sewage intrusion into drinking water: Microbial succession and organic transformation at molecular level
    Mengqing Fan, Anran Ren, Mingchen Yao, Xiaoming Li, Walter van der Meer, Guo Yu, Gertjan Medema, Joan Rose, Gang Liu
    Water Research.2024; 266: 122281.     CrossRef
  • Current status of intestinal parasite infections in fecal samples of dogs in Korea
    You-Jeong Lee, Beoul Kim, Dongmi Kwak, Min-Goo Seo
    Parasites, Hosts and Diseases.2024; 62(4): 438.     CrossRef
  • Molecular identification and antiprotozoal activity of silver nanoparticles on viability of Cryptosporidium parvum isolated from pigeons, pigeon fanciers and water
    Rasha M. M. Abou Elez, Amira S. A. Attia, Hala M. N. Tolba, Reham G. A. Anter, Ibrahim Elsohaby
    Scientific Reports.2023;[Epub]     CrossRef
  • Outbreak of severe diarrhea due to zoonotic Cryptosporidium parvum and C. xiaoi in goat kids in Chungcheongbuk-do, Korea
    Ah-Young Kim, Badriah Alkathiri, Subin Lee, Kyung-Duk Min, Soochong Kim, Sang-Myeong Lee, Wan-Kyu Lee, Dongmi Kwak, Seung-Hun Lee
    Parasitology Research.2023; 122(9): 2045.     CrossRef
  • Giardia spp. cysts and Cryptosporidium spp. oocysts in drinking water treatment residues: comparison of recovery methods for quantity assessment
    Kamila Jessie Sammarro Silva, Lyda Patricia Sabogal-Paz
    Environmental Technology.2021; 42(20): 3144.     CrossRef
  • Detection of Giardia and Cryptosporidium in environmental matrices with immunomagnetic separation: two or three acid dissociations
    Fernando César Andreoli, Lyda Patricia Sabogal-Paz
    Parasitology Research.2021; 120(2): 629.     CrossRef
  • Molecular Prevalence and Genotypes of Cryptosporidium parvum and Giardia duodenalis in Patients with Acute Diarrhea in Korea, 2013-2016
    Da-Won Ma, Myoung-Ro Lee, Sung-Hee Hong, Shin-Hyeong Cho, Sang-Eun Lee
    The Korean Journal of Parasitology.2019; 57(5): 531.     CrossRef
  • Monitoring of Noxious Protozoa for Management of Natural Water Resources
    Young Yil Bahk, Pyo Yun Cho, Sung Kyu Ahn, Sangjung Park, Won Hwa Jheong, Yun-Kyu Park, Ho-Joon Shin, Sang-Seob Lee, Okjae Rhee, Tong-Soo Kim
    The Korean Journal of Parasitology.2018; 56(2): 205.     CrossRef
  • 9,541 View
  • 119 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
  • 12,907 View
  • 175 Download
  • Crossref
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
  • 8,817 View
  • 82 Download
  • Crossref
A Case of Budd-Chiari Syndrome Associated with Alveolar Echinococcosis
Erol ?akmak, Hakan Alagozlu, Cesur Gumus, Celiks?z Al?
Korean J Parasitol 2013;51(4):475-477.
Published online August 30, 2013
DOI: https://doi.org/10.3347/kjp.2013.51.4.475

Although alveolar echinococcosis (AE) can cause a serious disease with high mortality and morbidity similar to malign neoplasms. A 62-year-old woman admitted to a hospital located in Sivas, Turkey, with the complaints of fatigue and right upper abdominal pain. On contrast abdominal CT, a 54×70×45 mm sized cystic lesion was detected in the left lobe of the liver that was seen to extend to the posterior mediastinum and invade the diaphragm, esophagus, and pericardium. The cystic lesion was seen to be occluding the inferior vena cava and left hepatic vein at the level where the hepatic veins poured into the inferior vena cava. Bilateral pleural effusion was also detected. We discussed this secondary Budd-Chiari Syndrome (BCS) case, resulting from the AE occlusion of the left hepatic vein and inferior vena cava, in light of the information in literature.

Citations

Citations to this article as recorded by  Crossref logo
  • A Case Series and Literature Review of Alveolar Echinococcosis in Kashmir, India: An Emerging Endemic Zone for Echinococcus multilocularis
    Mohammad Sultan Khuroo, Naira Sultan Khuroo, Ajaz Ahmad Rather
    Life.2024; 14(7): 794.     CrossRef
  • Role of the radiologist in the diagnosis and management of the two forms of hepatic echinococcosis
    Paul Calame, Mathieu Weck, Andreas Busse-Cote, Eleonore Brumpt, Carine Richou, Celia Turco, Alexandre Doussot, Solange Bresson-Hadni, Eric Delabrousse
    Insights into Imaging.2022;[Epub]     CrossRef
  • Intrahepatic manifestation and distant extrahepatic disease in alveolar echinococcosis: a multicenter cohort study
    Tilmann Graeter, Rong Shi, Haihua Bao, Wenya Liu, Weixia Li, Yi Jiang, Julian Schmidberger, Eleonore Brumpt, Eric Delabrousse, Wolfgang Kratzer
    Acta Radiologica.2021; 62(8): 997.     CrossRef
  • Evaluation of intrahepatic manifestation and distant extrahepatic disease in alveolar echinococcosis
    Tilmann Graeter, Hai-Hua Bao, Rong Shi, Wen-Ya Liu, Wei-Xia Li, Yi Jiang, Julian Schmidberger, Eleonore Brumpt, Eric Delabrousse, Wolfgang Kratzer, the XUUB Consortium
    World Journal of Gastroenterology.2020; 26(29): 4302.     CrossRef
  • Left trisectionectomy and supra-hepatic caval reconstruction with vascular prosthesis for chronic Budd-Chiari syndrome caused by hepatic alveolar echinococcosis
    Bo Ran, Tie-Min Jiang, Aimaiti Yasen, Abudusalamu Aini, Qiang Guo, Rui-Qing Zhang, Ying-Mei Shao, Hao Wen, Aji Tuerganaili
    Chinese Medical Journal.2019; 132(23): 2886.     CrossRef
  • A report on three patients with Echinococcus multilocularis: Lessons learned
    Nalini Bansal, Vivek Vij, Mukul Rastogi, Manav Wadhawan, Ajay Kumar
    Indian Journal of Gastroenterology.2018; 37(4): 353.     CrossRef
  • Diagnosis and treatment guidelines for aberrant portal hemodynamics

    Hepatology Research.2017; 47(5): 373.     CrossRef
  • Recurrent multiple-organ involvement of disseminated alveolar echinococcosis in 3 patients
    Leilei Xu, Sikandaer Siyiti, Xinghua Song, Hao Wen, Liwen Ding, Akbar Yunus, Zheng Tian, Chong Wang, Jiangtao Chen
    Medicine.2017; 96(42): e7632.     CrossRef
  • Orage pour ce foie mais pas de désespoir…
    C. Bernard, F. Bailly, F. Craigherot, B. Bancel, M. Brevet, C. Broussolle, P. Sève, P. Bélénotti
    La Revue de Médecine Interne.2015; 36(10): 706.     CrossRef
  • Hepatobiliary complications of alveolar echinococcosis: A long-term follow-up study
    Tilmann Graeter
    World Journal of Gastroenterology.2015; 21(16): 4925.     CrossRef
  • 8,589 View
  • 73 Download
  • Crossref
Brief Communications
Superoxide Anion Production by Human Neutrophils Activated by Trichomonas vaginalis
Hyun-Ouk Song, Jae-Sook Ryu
Korean J Parasitol 2013;51(4):479-484.
Published online August 30, 2013
DOI: https://doi.org/10.3347/kjp.2013.51.4.479

Neutrophils are the predominant inflammatory cells found in vaginal discharges of patients infected with Trichomonas vaginalis. In this study, we examined superoxide anion (O2.-) production by neutrophils activated by T. vaginalis. Human neutrophils produced superoxide anions when stimulated with either a lysate of T. vaginalis, its membrane component (MC), or excretory-secretory product (ESP). To assess the role of trichomonad protease in production of superoxide anions by neutrophils, T. vaginalis lysate, ESP, and MC were each pretreated with a protease inhibitor cocktail before incubation with neutrophils. Superoxide anion production was significantly decreased by this treatment. Trichomonad growth was inhibited by preincubation with supernatants of neutrophils incubated for 3 hr with T. vaginalis lysate. Furthermore, myeloperoxidase (MPO) production by neutrophils was stimulated by live trichomonads. These results indicate that the production of superoxide anions and MPO by neutrophils stimulated with T. vaginalis may be a part of defense mechanisms of neutrophils in trichomoniasis.

Citations

Citations to this article as recorded by  Crossref logo
  • IDO1 promotes Echinococcus multilocularis infection by regulating the formation of neutrophil extracellular traps
    Haining Zhang, Ru Meng, Fan Zhang, Ao Chen, Hongrun Ge, Wangkai Chen, Zhi Li, Yong Fu
    Veterinary Research.2025;[Epub]     CrossRef
  • Trichomonas vaginalis triggers neutrophil extracellular traps reducing parasite integrity and growth
    María G. Ramírez-Ledesma, Yordan J. Romero-Contreras, Mayra C. Rodríguez, Ruth Reyes-Cortes, Patricia Cuéllar-Mata, Eva E. Avila
    Parasitology Research.2022; 121(5): 1355.     CrossRef
  • Immunological Activities of Crude Polysaccharides Extracts ofClimacodon pulcherrimus(Phanerochaetaceae) in Lipopolysaccharide-Induced Rat Macrophages and Neutrophils' Responses
    Tume Christopher, Oumar Mahamat, Miyanui N. Chungong, C. Atemenkeh Ngwa, P. Maishu Samka
    Journal of Medicinal Food.2021; 24(2): 180.     CrossRef
  • Angiotensin‐converting enzyme as a new immunologic target for the new SARS‐CoV‐2
    Shahin Hallaj, Anahita Ghorbani, Seyed Ali Mousavi‐Aghdas, Mohammad Mirza‐Aghazadeh‐Attari, Andrey Sevbitov, Vida Hashemi, Tooba Hallaj, Farhad Jadidi‐Niaragh
    Immunology & Cell Biology.2021; 99(2): 192.     CrossRef
  • The state of art of neutrophil extracellular traps in protozoan and helminthic infections
    César Díaz-Godínez, Julio C. Carrero
    Bioscience Reports.2019;[Epub]     CrossRef
  • Recombinant α-actinin subunit antigens of Trichomonas vaginalis as potential vaccine candidates in protecting against trichomoniasis
    Yi-Ting Xie, Jiang-Mei Gao, Ya-Ping Wu, Petrus Tang, Geoff Hide, De-Hua Lai, Zhao-Rong Lun
    Parasites & Vectors.2017;[Epub]     CrossRef
  • Adenosine reduces reactive oxygen species and interleukin-8 production by Trichomonas vaginalis-stimulated neutrophils
    Amanda Piccoli Frasson, Camila Braz Menezes, Gustavo Krumel Goelzer, Simone Cristina Baggio Gnoatto, Solange Cristina Garcia, Tiana Tasca
    Purinergic Signalling.2017; 13(4): 569.     CrossRef
  • 9,466 View
  • 71 Download
  • Crossref
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
  • 8,765 View
  • 98 Download
  • Crossref
Paleoparasitological Surveys for Detection of Helminth Eggs in Archaeological Sites of Jeolla-do and Jeju-do
Myeong-Ju Kim, Dong Hoon Shin, Mi-Jin Song, Hye-Young Song, Min Seo
Korean J Parasitol 2013;51(4):489-492.
Published online August 30, 2013
DOI: https://doi.org/10.3347/kjp.2013.51.4.489

A paleoparasitological survey to detect helminth eggs was performed in archaeological sites of Jeolla-do and Jeju-do, the Republic of Korea. Total 593 soil samples were collected in 12 sites of Jeolla-do and 5 sites of Jeju-do from April to November 2011, and examined by the methods of Pike and coworkers. A total of 4 helminth eggs, 2 eggs each for Trichuris trichiura and Ascaris sp., were found in soil samples from 1 site, in Hyangyang-ri, Jangheung-eup, Jangheung-gun, Jeollanam-do. The egg-recovery layer was presumed to represent a 19th century farm, which fact suggested the use of human manures. This is the third archaeological discovery of parasite eggs in Jeolla-do. Additionally, no helminth eggs in archaeological sites of Jeju-do is an interesting problem to be solved in the further investigations.

Citations

Citations to this article as recorded by  Crossref logo
  • Paleoparasitology research on ancient helminth eggs and larvae in the Republic of Korea
    Jong-Yil Chai, Min Seo, Dong Hoon Shin
    Parasites, Hosts and Diseases.2023; 61(4): 345.     CrossRef
  • Discovery of Parasite Eggs in Archeological Residence during the 15th Century in Seoul, Korea
    Pyo Yeon Cho, Jung-Min Park, Myeong-Ki Hwang, Seo Hye Park, Yun-Kyu Park, Bo-Young Jeon, Tong-Soo Kim, Hyeong-Woo Lee
    The Korean Journal of Parasitology.2017; 55(3): 357.     CrossRef
  • Paleoparasitological study on the soil sediment samples from archaeological sites of ancient Silla Kingdom in Korean peninsula
    Myeung Ju Kim, Min Seo, Chang Seok Oh, Jong-Yil Chai, Jinju Lee, Gab-jin Kim, Won Young Ma, Soon Jo Choi, Karl Reinhard, Adauto Araujo, Dong Hoon Shin
    Quaternary International.2016; 405: 80.     CrossRef
  • 8,758 View
  • 79 Download
  • Crossref