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Development of a Nanobody-based lateral flow assay to detect active Trypanosoma congolense infections

Animal African trypanosomosis (AAT), a disease affecting livestock, is caused by parasites of the Trypanosoma genus (mainly T. vivax and T. congolense). AAT is widespread in Sub-Saharan Africa, where it continues to impose a heavy socio-economic burden as it renders development of sustainable livest...

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Autores principales: Pinto Torres, Joar E., Goossens, Julie, Ding, Jianzu, Li, Zeng, Lu, Shaohong, Vertommen, Didier, Naniima, Peter, Chen, Rui, Muyldermans, Serge, Sterckx, Yann G.-J., Magez, Stefan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5998082/
https://www.ncbi.nlm.nih.gov/pubmed/29899344
http://dx.doi.org/10.1038/s41598-018-26732-7
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author Pinto Torres, Joar E.
Goossens, Julie
Ding, Jianzu
Li, Zeng
Lu, Shaohong
Vertommen, Didier
Naniima, Peter
Chen, Rui
Muyldermans, Serge
Sterckx, Yann G.-J.
Magez, Stefan
author_facet Pinto Torres, Joar E.
Goossens, Julie
Ding, Jianzu
Li, Zeng
Lu, Shaohong
Vertommen, Didier
Naniima, Peter
Chen, Rui
Muyldermans, Serge
Sterckx, Yann G.-J.
Magez, Stefan
author_sort Pinto Torres, Joar E.
collection PubMed
description Animal African trypanosomosis (AAT), a disease affecting livestock, is caused by parasites of the Trypanosoma genus (mainly T. vivax and T. congolense). AAT is widespread in Sub-Saharan Africa, where it continues to impose a heavy socio-economic burden as it renders development of sustainable livestock rearing very strenuous. Active case-finding and the identification of infected animals prior to initiation of drug treatment requires the availability of sensitive and specific diagnostic tests. In this paper, we describe the development of two heterologous sandwich assay formats (ELISA and LFA) for T. congolense detection through the use of Nanobodies (Nbs). The immunisation of an alpaca with a secretome mix from two T. congolense strains resulted in the identification of a Nb pair (Nb44/Nb42) that specifically targets the glycolytic enzyme pyruvate kinase. We demonstrate that the Nb44/Nb42 ELISA and LFA can be employed to detect parasitaemia in plasma samples from experimentally infected mice and cattle and, additionally, that they can serve as ‘test-of-cure’ tools. Altogether, the findings in this paper present the development and evaluation of the first Nb-based antigen detection LFA to identify active T. congolense infections.
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spelling pubmed-59980822018-06-21 Development of a Nanobody-based lateral flow assay to detect active Trypanosoma congolense infections Pinto Torres, Joar E. Goossens, Julie Ding, Jianzu Li, Zeng Lu, Shaohong Vertommen, Didier Naniima, Peter Chen, Rui Muyldermans, Serge Sterckx, Yann G.-J. Magez, Stefan Sci Rep Article Animal African trypanosomosis (AAT), a disease affecting livestock, is caused by parasites of the Trypanosoma genus (mainly T. vivax and T. congolense). AAT is widespread in Sub-Saharan Africa, where it continues to impose a heavy socio-economic burden as it renders development of sustainable livestock rearing very strenuous. Active case-finding and the identification of infected animals prior to initiation of drug treatment requires the availability of sensitive and specific diagnostic tests. In this paper, we describe the development of two heterologous sandwich assay formats (ELISA and LFA) for T. congolense detection through the use of Nanobodies (Nbs). The immunisation of an alpaca with a secretome mix from two T. congolense strains resulted in the identification of a Nb pair (Nb44/Nb42) that specifically targets the glycolytic enzyme pyruvate kinase. We demonstrate that the Nb44/Nb42 ELISA and LFA can be employed to detect parasitaemia in plasma samples from experimentally infected mice and cattle and, additionally, that they can serve as ‘test-of-cure’ tools. Altogether, the findings in this paper present the development and evaluation of the first Nb-based antigen detection LFA to identify active T. congolense infections. Nature Publishing Group UK 2018-06-13 /pmc/articles/PMC5998082/ /pubmed/29899344 http://dx.doi.org/10.1038/s41598-018-26732-7 Text en © The Author(s) 2018 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Pinto Torres, Joar E.
Goossens, Julie
Ding, Jianzu
Li, Zeng
Lu, Shaohong
Vertommen, Didier
Naniima, Peter
Chen, Rui
Muyldermans, Serge
Sterckx, Yann G.-J.
Magez, Stefan
Development of a Nanobody-based lateral flow assay to detect active Trypanosoma congolense infections
title Development of a Nanobody-based lateral flow assay to detect active Trypanosoma congolense infections
title_full Development of a Nanobody-based lateral flow assay to detect active Trypanosoma congolense infections
title_fullStr Development of a Nanobody-based lateral flow assay to detect active Trypanosoma congolense infections
title_full_unstemmed Development of a Nanobody-based lateral flow assay to detect active Trypanosoma congolense infections
title_short Development of a Nanobody-based lateral flow assay to detect active Trypanosoma congolense infections
title_sort development of a nanobody-based lateral flow assay to detect active trypanosoma congolense infections
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5998082/
https://www.ncbi.nlm.nih.gov/pubmed/29899344
http://dx.doi.org/10.1038/s41598-018-26732-7
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