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Development of a microsphere-based immunoassay for the serological diagnosis of equine trypanosomosis

Trypanozoon infections in equids are caused by three parasite species in the Trypanozoon subgenus: Trypanosoma equiperdum, T. brucei and T. evansi. They are respectively responsible for infectious diseases dourine, nagana and surra. Due to the threat that Trypanozoon infection represents for interna...

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Autores principales: Verney, Mylène, Gautron, Morgane, Lemans, Charlène, Rincé, Alain, Hans, Aymeric, Hébert, Laurent
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8789838/
https://www.ncbi.nlm.nih.gov/pubmed/35079068
http://dx.doi.org/10.1038/s41598-022-05356-y
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author Verney, Mylène
Gautron, Morgane
Lemans, Charlène
Rincé, Alain
Hans, Aymeric
Hébert, Laurent
author_facet Verney, Mylène
Gautron, Morgane
Lemans, Charlène
Rincé, Alain
Hans, Aymeric
Hébert, Laurent
author_sort Verney, Mylène
collection PubMed
description Trypanozoon infections in equids are caused by three parasite species in the Trypanozoon subgenus: Trypanosoma equiperdum, T. brucei and T. evansi. They are respectively responsible for infectious diseases dourine, nagana and surra. Due to the threat that Trypanozoon infection represents for international horse trading, accurate diagnostic tests are crucial. Current tests suffer from poor sensitivity and specificity, due in the first case to the transient presence of parasites in the blood and in the second, to antigenic cross-reactivity among Trypanozoon subspecies. This study was designed to develop a microsphere‐based immunoassay for diagnosing equine trypanosomosis. We tested beads coated with eight Trypanosoma spp. recombinant antigens: enolase, GM6, PFR1, PFR2, ISG65, VSGat, RoTat1.2 and JN2118HU. Of these, GM6 was identified as the best candidate for the serological diagnosis of Trypanozoon infections in equids. Using a receiver operating characteristic (ROC) analysis on 349 equine sera, anti-GM6 antibodies were detected with an AUC value of 0.994 offering a sensitivity of 97.9% and a specificity of 96.0%. Our findings show that the GM6 antigen is a good target for diagnosing equine trypanosomosis using a microsphere‐based immunoassay. This promising assay could be a useful alternative to the official diagnostic tool for equine trypanosomosis.
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spelling pubmed-87898382022-01-27 Development of a microsphere-based immunoassay for the serological diagnosis of equine trypanosomosis Verney, Mylène Gautron, Morgane Lemans, Charlène Rincé, Alain Hans, Aymeric Hébert, Laurent Sci Rep Article Trypanozoon infections in equids are caused by three parasite species in the Trypanozoon subgenus: Trypanosoma equiperdum, T. brucei and T. evansi. They are respectively responsible for infectious diseases dourine, nagana and surra. Due to the threat that Trypanozoon infection represents for international horse trading, accurate diagnostic tests are crucial. Current tests suffer from poor sensitivity and specificity, due in the first case to the transient presence of parasites in the blood and in the second, to antigenic cross-reactivity among Trypanozoon subspecies. This study was designed to develop a microsphere‐based immunoassay for diagnosing equine trypanosomosis. We tested beads coated with eight Trypanosoma spp. recombinant antigens: enolase, GM6, PFR1, PFR2, ISG65, VSGat, RoTat1.2 and JN2118HU. Of these, GM6 was identified as the best candidate for the serological diagnosis of Trypanozoon infections in equids. Using a receiver operating characteristic (ROC) analysis on 349 equine sera, anti-GM6 antibodies were detected with an AUC value of 0.994 offering a sensitivity of 97.9% and a specificity of 96.0%. Our findings show that the GM6 antigen is a good target for diagnosing equine trypanosomosis using a microsphere‐based immunoassay. This promising assay could be a useful alternative to the official diagnostic tool for equine trypanosomosis. Nature Publishing Group UK 2022-01-25 /pmc/articles/PMC8789838/ /pubmed/35079068 http://dx.doi.org/10.1038/s41598-022-05356-y Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Verney, Mylène
Gautron, Morgane
Lemans, Charlène
Rincé, Alain
Hans, Aymeric
Hébert, Laurent
Development of a microsphere-based immunoassay for the serological diagnosis of equine trypanosomosis
title Development of a microsphere-based immunoassay for the serological diagnosis of equine trypanosomosis
title_full Development of a microsphere-based immunoassay for the serological diagnosis of equine trypanosomosis
title_fullStr Development of a microsphere-based immunoassay for the serological diagnosis of equine trypanosomosis
title_full_unstemmed Development of a microsphere-based immunoassay for the serological diagnosis of equine trypanosomosis
title_short Development of a microsphere-based immunoassay for the serological diagnosis of equine trypanosomosis
title_sort development of a microsphere-based immunoassay for the serological diagnosis of equine trypanosomosis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8789838/
https://www.ncbi.nlm.nih.gov/pubmed/35079068
http://dx.doi.org/10.1038/s41598-022-05356-y
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