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Proteomic Selection of Immunodiagnostic Antigens for Trypanosoma congolense

Animal African Trypanosomosis (AAT) presents a severe problem for agricultural development in sub-Saharan Africa. It is caused by several trypanosome species and current means of diagnosis are expensive and impractical for field use. Our aim was to discover antigens for the detection of antibodies t...

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Autores principales: Fleming, Jennifer R., Sastry, Lalitha, Crozier, Thomas W. M., Napier, Grant B., Sullivan, Lauren, Ferguson, Michael A. J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4055490/
https://www.ncbi.nlm.nih.gov/pubmed/24922510
http://dx.doi.org/10.1371/journal.pntd.0002936
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author Fleming, Jennifer R.
Sastry, Lalitha
Crozier, Thomas W. M.
Napier, Grant B.
Sullivan, Lauren
Ferguson, Michael A. J.
author_facet Fleming, Jennifer R.
Sastry, Lalitha
Crozier, Thomas W. M.
Napier, Grant B.
Sullivan, Lauren
Ferguson, Michael A. J.
author_sort Fleming, Jennifer R.
collection PubMed
description Animal African Trypanosomosis (AAT) presents a severe problem for agricultural development in sub-Saharan Africa. It is caused by several trypanosome species and current means of diagnosis are expensive and impractical for field use. Our aim was to discover antigens for the detection of antibodies to Trypanosoma congolense, one of the main causative agents of AAT. We took a proteomic approach to identify potential immunodiagnostic parasite protein antigens. One hundred and thirteen proteins were identified which were selectively recognized by infected cattle sera. These were assessed for likelihood of recombinant protein expression in E. coli and fifteen were successfully expressed and assessed for their immunodiagnostic potential by ELISA using pooled pre- and post-infection cattle sera. Three proteins, members of the invariant surface glycoprotein (ISG) family, performed favorably and were then assessed using individual cattle sera. One antigen, Tc38630, evaluated blind with 77 randomized cattle sera in an ELISA assay gave sensitivity and specificity performances of 87.2% and 97.4%, respectively. Cattle immunoreactivity to this antigen diminished significantly following drug-cure, a feature helpful for monitoring the efficacy of drug treatment.
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spelling pubmed-40554902014-06-18 Proteomic Selection of Immunodiagnostic Antigens for Trypanosoma congolense Fleming, Jennifer R. Sastry, Lalitha Crozier, Thomas W. M. Napier, Grant B. Sullivan, Lauren Ferguson, Michael A. J. PLoS Negl Trop Dis Research Article Animal African Trypanosomosis (AAT) presents a severe problem for agricultural development in sub-Saharan Africa. It is caused by several trypanosome species and current means of diagnosis are expensive and impractical for field use. Our aim was to discover antigens for the detection of antibodies to Trypanosoma congolense, one of the main causative agents of AAT. We took a proteomic approach to identify potential immunodiagnostic parasite protein antigens. One hundred and thirteen proteins were identified which were selectively recognized by infected cattle sera. These were assessed for likelihood of recombinant protein expression in E. coli and fifteen were successfully expressed and assessed for their immunodiagnostic potential by ELISA using pooled pre- and post-infection cattle sera. Three proteins, members of the invariant surface glycoprotein (ISG) family, performed favorably and were then assessed using individual cattle sera. One antigen, Tc38630, evaluated blind with 77 randomized cattle sera in an ELISA assay gave sensitivity and specificity performances of 87.2% and 97.4%, respectively. Cattle immunoreactivity to this antigen diminished significantly following drug-cure, a feature helpful for monitoring the efficacy of drug treatment. Public Library of Science 2014-06-12 /pmc/articles/PMC4055490/ /pubmed/24922510 http://dx.doi.org/10.1371/journal.pntd.0002936 Text en © 2014 Fleming et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Fleming, Jennifer R.
Sastry, Lalitha
Crozier, Thomas W. M.
Napier, Grant B.
Sullivan, Lauren
Ferguson, Michael A. J.
Proteomic Selection of Immunodiagnostic Antigens for Trypanosoma congolense
title Proteomic Selection of Immunodiagnostic Antigens for Trypanosoma congolense
title_full Proteomic Selection of Immunodiagnostic Antigens for Trypanosoma congolense
title_fullStr Proteomic Selection of Immunodiagnostic Antigens for Trypanosoma congolense
title_full_unstemmed Proteomic Selection of Immunodiagnostic Antigens for Trypanosoma congolense
title_short Proteomic Selection of Immunodiagnostic Antigens for Trypanosoma congolense
title_sort proteomic selection of immunodiagnostic antigens for trypanosoma congolense
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4055490/
https://www.ncbi.nlm.nih.gov/pubmed/24922510
http://dx.doi.org/10.1371/journal.pntd.0002936
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