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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2018
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.
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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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