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Mycobacterium vaccae induces a strong Th1 response that subsequently declines in C57BL/6 mice
Mycobacterium (M.) vaccae is a fast-growing species of saprophytic bacteria that is widely distributed. To understand the host immune responses induced by M. vaccae isolated from bovine submaxillary lymph nodes, C57BL/6 mice were infected with reference strain M. vaccae Bacillus Calmette-Guérin (BCG...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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The Korean Society of Veterinary Science
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5204028/ https://www.ncbi.nlm.nih.gov/pubmed/27994210 http://dx.doi.org/10.4142/jvs.2016.17.4.505 |
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author | Zhang, Lijiao Jiang, Yanlong Cui, Ziyin Yang, Wentao Yue, Limin Ma, Yingcong Shi, Shaohua Wang, Chunfang Wang, Chunfeng Qian, Aidong |
author_facet | Zhang, Lijiao Jiang, Yanlong Cui, Ziyin Yang, Wentao Yue, Limin Ma, Yingcong Shi, Shaohua Wang, Chunfang Wang, Chunfeng Qian, Aidong |
author_sort | Zhang, Lijiao |
collection | PubMed |
description | Mycobacterium (M.) vaccae is a fast-growing species of saprophytic bacteria that is widely distributed. To understand the host immune responses induced by M. vaccae isolated from bovine submaxillary lymph nodes, C57BL/6 mice were infected with reference strain M. vaccae Bacillus Calmette-Guérin (BCG) and isolated M. vaccae using intraperitoneal injections. Comparison of the bacterial replication and organ pathology between M. vaccae and M. vaccae BCG revealed that M. vaccae was more malignant than M. vaccae in mice. We also demonstrated that serum from the M. vaccae-infected mice contained a higher expression level of gamma-interferon (IFN-γ), tumor necrosis factor alpha, monocyte chemoattractant protein-1, interleukin (IL)-4, IL-12, IL-10 and transforming growth factor beta than did the other groups, especially after week 4. Furthermore, when the numbers of CD3(+)CD4(+)IFN-γ(+) and CD3(+)CD4(+)IL4(+) cells in the infected mice were observed by flow cytometry, we found that a powerful T helper 1 (Th1) response was induced by M. vaccae infection, which was associated with the emergence of CD3(+)CD4(+)IFN-γ(+) cells. However, the Th1 response declined over time, which was associated with appearance of the CD4(+)CD25(+)FoxP3(+) and CD4(+)CD25(+)CD152(+)Treg cell reaction. In addition, a strong Th2 response was found. Finally, we found that M. vaccae infection increased the production of type I IFNs, which was associated with a reduced Th1 response. |
format | Online Article Text |
id | pubmed-5204028 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | The Korean Society of Veterinary Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-52040282017-01-04 Mycobacterium vaccae induces a strong Th1 response that subsequently declines in C57BL/6 mice Zhang, Lijiao Jiang, Yanlong Cui, Ziyin Yang, Wentao Yue, Limin Ma, Yingcong Shi, Shaohua Wang, Chunfang Wang, Chunfeng Qian, Aidong J Vet Sci Original Article Mycobacterium (M.) vaccae is a fast-growing species of saprophytic bacteria that is widely distributed. To understand the host immune responses induced by M. vaccae isolated from bovine submaxillary lymph nodes, C57BL/6 mice were infected with reference strain M. vaccae Bacillus Calmette-Guérin (BCG) and isolated M. vaccae using intraperitoneal injections. Comparison of the bacterial replication and organ pathology between M. vaccae and M. vaccae BCG revealed that M. vaccae was more malignant than M. vaccae in mice. We also demonstrated that serum from the M. vaccae-infected mice contained a higher expression level of gamma-interferon (IFN-γ), tumor necrosis factor alpha, monocyte chemoattractant protein-1, interleukin (IL)-4, IL-12, IL-10 and transforming growth factor beta than did the other groups, especially after week 4. Furthermore, when the numbers of CD3(+)CD4(+)IFN-γ(+) and CD3(+)CD4(+)IL4(+) cells in the infected mice were observed by flow cytometry, we found that a powerful T helper 1 (Th1) response was induced by M. vaccae infection, which was associated with the emergence of CD3(+)CD4(+)IFN-γ(+) cells. However, the Th1 response declined over time, which was associated with appearance of the CD4(+)CD25(+)FoxP3(+) and CD4(+)CD25(+)CD152(+)Treg cell reaction. In addition, a strong Th2 response was found. Finally, we found that M. vaccae infection increased the production of type I IFNs, which was associated with a reduced Th1 response. The Korean Society of Veterinary Science 2016-12 2016-12-20 /pmc/articles/PMC5204028/ /pubmed/27994210 http://dx.doi.org/10.4142/jvs.2016.17.4.505 Text en © 2016 The Korean Society of Veterinary Science. http://creativecommons.org/licenses/by-nc/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Zhang, Lijiao Jiang, Yanlong Cui, Ziyin Yang, Wentao Yue, Limin Ma, Yingcong Shi, Shaohua Wang, Chunfang Wang, Chunfeng Qian, Aidong Mycobacterium vaccae induces a strong Th1 response that subsequently declines in C57BL/6 mice |
title | Mycobacterium vaccae induces a strong Th1 response that subsequently declines in C57BL/6 mice |
title_full | Mycobacterium vaccae induces a strong Th1 response that subsequently declines in C57BL/6 mice |
title_fullStr | Mycobacterium vaccae induces a strong Th1 response that subsequently declines in C57BL/6 mice |
title_full_unstemmed | Mycobacterium vaccae induces a strong Th1 response that subsequently declines in C57BL/6 mice |
title_short | Mycobacterium vaccae induces a strong Th1 response that subsequently declines in C57BL/6 mice |
title_sort | mycobacterium vaccae induces a strong th1 response that subsequently declines in c57bl/6 mice |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5204028/ https://www.ncbi.nlm.nih.gov/pubmed/27994210 http://dx.doi.org/10.4142/jvs.2016.17.4.505 |
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