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Baseline analysis of Mycoplasma mycoides subsp. mycoides antigens as targets for a DIVA assay for use with a subunit vaccine for contagious bovine pleuropneumonia

BACKGROUND: Mycoplasma mycoides subsp. mycoides (Mmm) is the causative agent of contagious bovine pleuropneumonia in cattle. A prototype subunit vaccine is being developed, however, there is currently no diagnostic test that can differentiate between infected cattle and those vaccinated with the pro...

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Autores principales: Lutta, Harrison O., Odongo, David, Mather, Arshad, Perez-Casal, Jose, Potter, Andrew, Gerdts, Volker, Berberov, Emil M., Prysliak, Tracy, Kyallo, Martina, Kipronoh, Alexander, Olum, Moses, Pelle, Roger, Naessens, Jan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7350692/
https://www.ncbi.nlm.nih.gov/pubmed/32650780
http://dx.doi.org/10.1186/s12917-020-02453-w
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author Lutta, Harrison O.
Odongo, David
Mather, Arshad
Perez-Casal, Jose
Potter, Andrew
Gerdts, Volker
Berberov, Emil M.
Prysliak, Tracy
Kyallo, Martina
Kipronoh, Alexander
Olum, Moses
Pelle, Roger
Naessens, Jan
author_facet Lutta, Harrison O.
Odongo, David
Mather, Arshad
Perez-Casal, Jose
Potter, Andrew
Gerdts, Volker
Berberov, Emil M.
Prysliak, Tracy
Kyallo, Martina
Kipronoh, Alexander
Olum, Moses
Pelle, Roger
Naessens, Jan
author_sort Lutta, Harrison O.
collection PubMed
description BACKGROUND: Mycoplasma mycoides subsp. mycoides (Mmm) is the causative agent of contagious bovine pleuropneumonia in cattle. A prototype subunit vaccine is being developed, however, there is currently no diagnostic test that can differentiate between infected cattle and those vaccinated with the prototype subunit vaccine. This study characterized Mmm proteins to identify potential antigens for use in differentiating infected from vaccinated animals. RESULTS: Ten Mmm antigens expressed as recombinant proteins were tested in an indirect ELISA using experimental sera from control groups, infected, and vaccinated animals. Data were imported into R software for analysis and drawing of the box and scatter plots while Cohen’s Kappa assessed the level of agreement between the Mmm antigens. Two vaccine antigens (MSC_0499 and MSC_0776) were superior in detecting antibodies in sera of animals vaccinated with the subunit vaccines while two non-vaccine antigens (MSC_0636 and LppB) detected antibodies in sera of infected animals showing all clinical stages of the disease. Sensitivity and specificity of above 87.5% were achieved when the MSC_0499 and MSC_0636 antigens were tested on sera from vaccinated and infected animals. CONCLUSIONS: The MSC_0499 and MSC_0776 antigens were the most promising for detecting vaccinated animals, while MSC_0636 and LppB were the best targets to identify infected animals. Further testing of sera from vaccinated and infected animals collected at different time intervals in the field should help establish how useful a diagnostic test based on a cocktail of these proteins would be.
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spelling pubmed-73506922020-07-14 Baseline analysis of Mycoplasma mycoides subsp. mycoides antigens as targets for a DIVA assay for use with a subunit vaccine for contagious bovine pleuropneumonia Lutta, Harrison O. Odongo, David Mather, Arshad Perez-Casal, Jose Potter, Andrew Gerdts, Volker Berberov, Emil M. Prysliak, Tracy Kyallo, Martina Kipronoh, Alexander Olum, Moses Pelle, Roger Naessens, Jan BMC Vet Res Research Article BACKGROUND: Mycoplasma mycoides subsp. mycoides (Mmm) is the causative agent of contagious bovine pleuropneumonia in cattle. A prototype subunit vaccine is being developed, however, there is currently no diagnostic test that can differentiate between infected cattle and those vaccinated with the prototype subunit vaccine. This study characterized Mmm proteins to identify potential antigens for use in differentiating infected from vaccinated animals. RESULTS: Ten Mmm antigens expressed as recombinant proteins were tested in an indirect ELISA using experimental sera from control groups, infected, and vaccinated animals. Data were imported into R software for analysis and drawing of the box and scatter plots while Cohen’s Kappa assessed the level of agreement between the Mmm antigens. Two vaccine antigens (MSC_0499 and MSC_0776) were superior in detecting antibodies in sera of animals vaccinated with the subunit vaccines while two non-vaccine antigens (MSC_0636 and LppB) detected antibodies in sera of infected animals showing all clinical stages of the disease. Sensitivity and specificity of above 87.5% were achieved when the MSC_0499 and MSC_0636 antigens were tested on sera from vaccinated and infected animals. CONCLUSIONS: The MSC_0499 and MSC_0776 antigens were the most promising for detecting vaccinated animals, while MSC_0636 and LppB were the best targets to identify infected animals. Further testing of sera from vaccinated and infected animals collected at different time intervals in the field should help establish how useful a diagnostic test based on a cocktail of these proteins would be. BioMed Central 2020-07-10 /pmc/articles/PMC7350692/ /pubmed/32650780 http://dx.doi.org/10.1186/s12917-020-02453-w Text en © The Author(s) 2020 Open AccessThis 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/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Lutta, Harrison O.
Odongo, David
Mather, Arshad
Perez-Casal, Jose
Potter, Andrew
Gerdts, Volker
Berberov, Emil M.
Prysliak, Tracy
Kyallo, Martina
Kipronoh, Alexander
Olum, Moses
Pelle, Roger
Naessens, Jan
Baseline analysis of Mycoplasma mycoides subsp. mycoides antigens as targets for a DIVA assay for use with a subunit vaccine for contagious bovine pleuropneumonia
title Baseline analysis of Mycoplasma mycoides subsp. mycoides antigens as targets for a DIVA assay for use with a subunit vaccine for contagious bovine pleuropneumonia
title_full Baseline analysis of Mycoplasma mycoides subsp. mycoides antigens as targets for a DIVA assay for use with a subunit vaccine for contagious bovine pleuropneumonia
title_fullStr Baseline analysis of Mycoplasma mycoides subsp. mycoides antigens as targets for a DIVA assay for use with a subunit vaccine for contagious bovine pleuropneumonia
title_full_unstemmed Baseline analysis of Mycoplasma mycoides subsp. mycoides antigens as targets for a DIVA assay for use with a subunit vaccine for contagious bovine pleuropneumonia
title_short Baseline analysis of Mycoplasma mycoides subsp. mycoides antigens as targets for a DIVA assay for use with a subunit vaccine for contagious bovine pleuropneumonia
title_sort baseline analysis of mycoplasma mycoides subsp. mycoides antigens as targets for a diva assay for use with a subunit vaccine for contagious bovine pleuropneumonia
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7350692/
https://www.ncbi.nlm.nih.gov/pubmed/32650780
http://dx.doi.org/10.1186/s12917-020-02453-w
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