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Antibody response to a sterile filtered PPD tuberculin in M. bovis infected and M. bovis sensitized cattle
BACKGROUND: Bovine tuberculosis, caused by Mycobacterium bovis, afflicts approximately 50 million cattle worldwide and is detected by the tuberculin skin test (TST). While it has long been recognized that purified protein derivative (PPD) tuberculin is composed of a mixture of M. bovis derived prote...
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2010
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2994848/ https://www.ncbi.nlm.nih.gov/pubmed/21062483 http://dx.doi.org/10.1186/1746-6148-6-50 |
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author | Rennie, Bryan Filion, Lionel G Smart, Nonie |
author_facet | Rennie, Bryan Filion, Lionel G Smart, Nonie |
author_sort | Rennie, Bryan |
collection | PubMed |
description | BACKGROUND: Bovine tuberculosis, caused by Mycobacterium bovis, afflicts approximately 50 million cattle worldwide and is detected by the tuberculin skin test (TST). While it has long been recognized that purified protein derivative (PPD) tuberculin is composed of a mixture of M. bovis derived protein components, little is known about the quality, relative quantity and identity of the proteins that make up PPD tuberculin. We manufactured a sterile filtered PPD tuberculin (SF-PPD) from a nine-week-old M. bovis culture supernatant in order to characterise the culture filtrate proteins (CFP) which make up M. bovis PPD tuberculin and to compare the antibody response of M. bovis infected versus M. bovis sensitized cattle. RESULTS: SF-PPD resolved into approximately 200 discrete spots using two-dimensional polyacrylamide gel electrophoresis (2-DE) while fewer than 65 spots could be discerned from 2-DE gels of tuberculin derived from autoclaved culture supernatant. Two dimensional Western blot analyses indicated that sera from M. bovis sensitized cattle recognized additional SF-PPD antigens as compared to M. bovis infected cattle at seven weeks post infection/sensitization. However, application of a comparative tuberculin skin test resulted in an antibody boosting response to the same set of M. bovis CFPs in both the M. bovis infected and M. bovis sensitized cattle. CONCLUSIONS: We concluded that it is the heat sterilization of the M. bovis CFPs that causes severe structural changes to the M. bovis proteins. This work suggests that M. bovis infected cattle and cattle artificially sensitized to M. bovis with an injection of heat killed cells exhibit similar antibody responses to M. bovis antigens. |
format | Text |
id | pubmed-2994848 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-29948482010-12-01 Antibody response to a sterile filtered PPD tuberculin in M. bovis infected and M. bovis sensitized cattle Rennie, Bryan Filion, Lionel G Smart, Nonie BMC Vet Res Research Article BACKGROUND: Bovine tuberculosis, caused by Mycobacterium bovis, afflicts approximately 50 million cattle worldwide and is detected by the tuberculin skin test (TST). While it has long been recognized that purified protein derivative (PPD) tuberculin is composed of a mixture of M. bovis derived protein components, little is known about the quality, relative quantity and identity of the proteins that make up PPD tuberculin. We manufactured a sterile filtered PPD tuberculin (SF-PPD) from a nine-week-old M. bovis culture supernatant in order to characterise the culture filtrate proteins (CFP) which make up M. bovis PPD tuberculin and to compare the antibody response of M. bovis infected versus M. bovis sensitized cattle. RESULTS: SF-PPD resolved into approximately 200 discrete spots using two-dimensional polyacrylamide gel electrophoresis (2-DE) while fewer than 65 spots could be discerned from 2-DE gels of tuberculin derived from autoclaved culture supernatant. Two dimensional Western blot analyses indicated that sera from M. bovis sensitized cattle recognized additional SF-PPD antigens as compared to M. bovis infected cattle at seven weeks post infection/sensitization. However, application of a comparative tuberculin skin test resulted in an antibody boosting response to the same set of M. bovis CFPs in both the M. bovis infected and M. bovis sensitized cattle. CONCLUSIONS: We concluded that it is the heat sterilization of the M. bovis CFPs that causes severe structural changes to the M. bovis proteins. This work suggests that M. bovis infected cattle and cattle artificially sensitized to M. bovis with an injection of heat killed cells exhibit similar antibody responses to M. bovis antigens. BioMed Central 2010-11-09 /pmc/articles/PMC2994848/ /pubmed/21062483 http://dx.doi.org/10.1186/1746-6148-6-50 Text en Copyright ©2010 Rennie et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Rennie, Bryan Filion, Lionel G Smart, Nonie Antibody response to a sterile filtered PPD tuberculin in M. bovis infected and M. bovis sensitized cattle |
title | Antibody response to a sterile filtered PPD tuberculin in M. bovis infected and M. bovis sensitized cattle |
title_full | Antibody response to a sterile filtered PPD tuberculin in M. bovis infected and M. bovis sensitized cattle |
title_fullStr | Antibody response to a sterile filtered PPD tuberculin in M. bovis infected and M. bovis sensitized cattle |
title_full_unstemmed | Antibody response to a sterile filtered PPD tuberculin in M. bovis infected and M. bovis sensitized cattle |
title_short | Antibody response to a sterile filtered PPD tuberculin in M. bovis infected and M. bovis sensitized cattle |
title_sort | antibody response to a sterile filtered ppd tuberculin in m. bovis infected and m. bovis sensitized cattle |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2994848/ https://www.ncbi.nlm.nih.gov/pubmed/21062483 http://dx.doi.org/10.1186/1746-6148-6-50 |
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