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Bovine Staphylococcus aureus Superantigens Stimulate the Entire T Cell Repertoire of Cattle
Superantigens (SAgs) represent a diverse family of bacterial toxins that induce Vβ-specific T cell proliferation associated with an array of important diseases in humans and animals, including mastitis of dairy cows. However, an understanding of the diversity and distribution of SAg genes among bovi...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Microbiology
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6204692/ https://www.ncbi.nlm.nih.gov/pubmed/30201699 http://dx.doi.org/10.1128/IAI.00505-18 |
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author | Wilson, Gillian J. Tuffs, Stephen W. Wee, Bryan A. Seo, Keun Seok Park, Nogi Connelley, Timothy Guinane, Caitriona M. Morrison, W. Ivan Fitzgerald, J. Ross |
author_facet | Wilson, Gillian J. Tuffs, Stephen W. Wee, Bryan A. Seo, Keun Seok Park, Nogi Connelley, Timothy Guinane, Caitriona M. Morrison, W. Ivan Fitzgerald, J. Ross |
author_sort | Wilson, Gillian J. |
collection | PubMed |
description | Superantigens (SAgs) represent a diverse family of bacterial toxins that induce Vβ-specific T cell proliferation associated with an array of important diseases in humans and animals, including mastitis of dairy cows. However, an understanding of the diversity and distribution of SAg genes among bovine Staphylococcus aureus strains and their role in the pathogenesis of mastitis is lacking. Population genomic analysis of 195 bovine S. aureus isolates representing 57 unique sequence types revealed that strains encode 2 to 13 distinct SAgs and that the majority of isolates contain 5 or more SAg genes. A genome-scale analysis of bovine reference strain RF122 revealed a complement of 11 predicted SAg genes, which were all expressed in vitro. Detection of specific antibodies in convalescent cows suggests expression of 7 of 11 SAgs during natural S. aureus infection. We determined the Vβ T cell activation profile for all functional SAgs encoded by RF122, revealing evidence for bovine host-specific activity among the recently identified RF122-encoded SAgs SElY and SElZ. Remarkably, we discovered that some strains have evolved the capacity to stimulate the entire T cell repertoire of cattle through an array of diverse SAgs, suggesting a key role in bovine immune evasion. |
format | Online Article Text |
id | pubmed-6204692 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | American Society for Microbiology |
record_format | MEDLINE/PubMed |
spelling | pubmed-62046922018-11-15 Bovine Staphylococcus aureus Superantigens Stimulate the Entire T Cell Repertoire of Cattle Wilson, Gillian J. Tuffs, Stephen W. Wee, Bryan A. Seo, Keun Seok Park, Nogi Connelley, Timothy Guinane, Caitriona M. Morrison, W. Ivan Fitzgerald, J. Ross Infect Immun Molecular Pathogenesis Superantigens (SAgs) represent a diverse family of bacterial toxins that induce Vβ-specific T cell proliferation associated with an array of important diseases in humans and animals, including mastitis of dairy cows. However, an understanding of the diversity and distribution of SAg genes among bovine Staphylococcus aureus strains and their role in the pathogenesis of mastitis is lacking. Population genomic analysis of 195 bovine S. aureus isolates representing 57 unique sequence types revealed that strains encode 2 to 13 distinct SAgs and that the majority of isolates contain 5 or more SAg genes. A genome-scale analysis of bovine reference strain RF122 revealed a complement of 11 predicted SAg genes, which were all expressed in vitro. Detection of specific antibodies in convalescent cows suggests expression of 7 of 11 SAgs during natural S. aureus infection. We determined the Vβ T cell activation profile for all functional SAgs encoded by RF122, revealing evidence for bovine host-specific activity among the recently identified RF122-encoded SAgs SElY and SElZ. Remarkably, we discovered that some strains have evolved the capacity to stimulate the entire T cell repertoire of cattle through an array of diverse SAgs, suggesting a key role in bovine immune evasion. American Society for Microbiology 2018-10-25 /pmc/articles/PMC6204692/ /pubmed/30201699 http://dx.doi.org/10.1128/IAI.00505-18 Text en Copyright © 2018 Wilson et al. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Molecular Pathogenesis Wilson, Gillian J. Tuffs, Stephen W. Wee, Bryan A. Seo, Keun Seok Park, Nogi Connelley, Timothy Guinane, Caitriona M. Morrison, W. Ivan Fitzgerald, J. Ross Bovine Staphylococcus aureus Superantigens Stimulate the Entire T Cell Repertoire of Cattle |
title | Bovine Staphylococcus aureus Superantigens Stimulate the Entire T Cell Repertoire of Cattle |
title_full | Bovine Staphylococcus aureus Superantigens Stimulate the Entire T Cell Repertoire of Cattle |
title_fullStr | Bovine Staphylococcus aureus Superantigens Stimulate the Entire T Cell Repertoire of Cattle |
title_full_unstemmed | Bovine Staphylococcus aureus Superantigens Stimulate the Entire T Cell Repertoire of Cattle |
title_short | Bovine Staphylococcus aureus Superantigens Stimulate the Entire T Cell Repertoire of Cattle |
title_sort | bovine staphylococcus aureus superantigens stimulate the entire t cell repertoire of cattle |
topic | Molecular Pathogenesis |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6204692/ https://www.ncbi.nlm.nih.gov/pubmed/30201699 http://dx.doi.org/10.1128/IAI.00505-18 |
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