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Investigation of the cause of geographic disparities in IDEXX ELISA sensitivity in serum samples from Mycobacterium bovis-infected cattle

Accurately identifying Mycobacterium bovis-infected cattle is critical for bovine tuberculosis prevention and control. One method for identifying infected cattle is an ELISA developed by IDEXX laboratories, which detects antibodies to two M. bovis proteins, MPB70 and MPB83. The assay’s sensitivity v...

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Autores principales: Trost, Brett, Stuber, Tod, Surujballi, Om, Nelson, Jeffrey, Robbe-Austerman, Suelee, Smith, Noel H., Desautels, Louis, Tikoo, Suresh K., Griebel, Philip
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4780098/
https://www.ncbi.nlm.nih.gov/pubmed/26949166
http://dx.doi.org/10.1038/srep22763
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author Trost, Brett
Stuber, Tod
Surujballi, Om
Nelson, Jeffrey
Robbe-Austerman, Suelee
Smith, Noel H.
Desautels, Louis
Tikoo, Suresh K.
Griebel, Philip
author_facet Trost, Brett
Stuber, Tod
Surujballi, Om
Nelson, Jeffrey
Robbe-Austerman, Suelee
Smith, Noel H.
Desautels, Louis
Tikoo, Suresh K.
Griebel, Philip
author_sort Trost, Brett
collection PubMed
description Accurately identifying Mycobacterium bovis-infected cattle is critical for bovine tuberculosis prevention and control. One method for identifying infected cattle is an ELISA developed by IDEXX laboratories, which detects antibodies to two M. bovis proteins, MPB70 and MPB83. The assay’s sensitivity varies by geographic region, with sensitivities of 77%, 45%, and 9% in bovine serum samples from the United Kingdom (n = 126), the United States (n = 146), and Mexico (n = 128), respectively. We hypothesized that geographically-biased sequence variation in mpb70 and mpb83, or in the genes that regulate their expression (sigK and rskA), may explain these differing sensitivities. This hypothesis was tested by comparing the sequences of these four genes in 455 M. bovis strains isolated from cattle in the aforementioned countries. For each gene, a single, common sequence was identified in most genomes of the M. bovis strains collected in all three countries. Twelve of the 455 strains were isolated from infected cattle for which the IDEXX ELISA was also performed. Five of the seven ELISA-positive genomes and three of the five ELISA-negative genomes contained the most common sequence of all four genes. Thus, sequence variation in mpb70, mpb83, sigK, and rskA does not explain the geographic disparities in IDEXX ELISA sensitivity.
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spelling pubmed-47800982016-03-09 Investigation of the cause of geographic disparities in IDEXX ELISA sensitivity in serum samples from Mycobacterium bovis-infected cattle Trost, Brett Stuber, Tod Surujballi, Om Nelson, Jeffrey Robbe-Austerman, Suelee Smith, Noel H. Desautels, Louis Tikoo, Suresh K. Griebel, Philip Sci Rep Article Accurately identifying Mycobacterium bovis-infected cattle is critical for bovine tuberculosis prevention and control. One method for identifying infected cattle is an ELISA developed by IDEXX laboratories, which detects antibodies to two M. bovis proteins, MPB70 and MPB83. The assay’s sensitivity varies by geographic region, with sensitivities of 77%, 45%, and 9% in bovine serum samples from the United Kingdom (n = 126), the United States (n = 146), and Mexico (n = 128), respectively. We hypothesized that geographically-biased sequence variation in mpb70 and mpb83, or in the genes that regulate their expression (sigK and rskA), may explain these differing sensitivities. This hypothesis was tested by comparing the sequences of these four genes in 455 M. bovis strains isolated from cattle in the aforementioned countries. For each gene, a single, common sequence was identified in most genomes of the M. bovis strains collected in all three countries. Twelve of the 455 strains were isolated from infected cattle for which the IDEXX ELISA was also performed. Five of the seven ELISA-positive genomes and three of the five ELISA-negative genomes contained the most common sequence of all four genes. Thus, sequence variation in mpb70, mpb83, sigK, and rskA does not explain the geographic disparities in IDEXX ELISA sensitivity. Nature Publishing Group 2016-03-07 /pmc/articles/PMC4780098/ /pubmed/26949166 http://dx.doi.org/10.1038/srep22763 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Trost, Brett
Stuber, Tod
Surujballi, Om
Nelson, Jeffrey
Robbe-Austerman, Suelee
Smith, Noel H.
Desautels, Louis
Tikoo, Suresh K.
Griebel, Philip
Investigation of the cause of geographic disparities in IDEXX ELISA sensitivity in serum samples from Mycobacterium bovis-infected cattle
title Investigation of the cause of geographic disparities in IDEXX ELISA sensitivity in serum samples from Mycobacterium bovis-infected cattle
title_full Investigation of the cause of geographic disparities in IDEXX ELISA sensitivity in serum samples from Mycobacterium bovis-infected cattle
title_fullStr Investigation of the cause of geographic disparities in IDEXX ELISA sensitivity in serum samples from Mycobacterium bovis-infected cattle
title_full_unstemmed Investigation of the cause of geographic disparities in IDEXX ELISA sensitivity in serum samples from Mycobacterium bovis-infected cattle
title_short Investigation of the cause of geographic disparities in IDEXX ELISA sensitivity in serum samples from Mycobacterium bovis-infected cattle
title_sort investigation of the cause of geographic disparities in idexx elisa sensitivity in serum samples from mycobacterium bovis-infected cattle
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4780098/
https://www.ncbi.nlm.nih.gov/pubmed/26949166
http://dx.doi.org/10.1038/srep22763
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