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Recombination-mediated remodelling of host–pathogen interactions during Staphylococcus aureus niche adaptation

Large-scale recombination events have led to the emergence of epidemic clones of several major bacterial pathogens. However, the functional impact of the recombination on clonal success is not understood. Here, we identified a novel widespread hybrid clone (ST71) of livestock-associated Staphylococc...

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Autores principales: Spoor, Laura E., Richardson, Emily, Richards, Amy C., Wilson, Gillian J., Mendonca, Chriselle, Gupta, Ravi Kr., McAdam, Paul R., Nutbeam-Tuffs, Stephen, Black, Nikki S., O'Gara, James P., Lee, Chia Y., Corander, Jukka, Ross Fitzgerald, J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Microbiology Society 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5320625/
https://www.ncbi.nlm.nih.gov/pubmed/28348819
http://dx.doi.org/10.1099/mgen.0.000036
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author Spoor, Laura E.
Richardson, Emily
Richards, Amy C.
Wilson, Gillian J.
Mendonca, Chriselle
Gupta, Ravi Kr.
McAdam, Paul R.
Nutbeam-Tuffs, Stephen
Black, Nikki S.
O'Gara, James P.
Lee, Chia Y.
Corander, Jukka
Ross Fitzgerald, J.
author_facet Spoor, Laura E.
Richardson, Emily
Richards, Amy C.
Wilson, Gillian J.
Mendonca, Chriselle
Gupta, Ravi Kr.
McAdam, Paul R.
Nutbeam-Tuffs, Stephen
Black, Nikki S.
O'Gara, James P.
Lee, Chia Y.
Corander, Jukka
Ross Fitzgerald, J.
author_sort Spoor, Laura E.
collection PubMed
description Large-scale recombination events have led to the emergence of epidemic clones of several major bacterial pathogens. However, the functional impact of the recombination on clonal success is not understood. Here, we identified a novel widespread hybrid clone (ST71) of livestock-associated Staphylococcus aureus that evolved from an ancestor belonging to the major bovine lineage CC97, through multiple large-scale recombination events with other S. aureus lineages occupying the same ruminant niche. The recombination events, affecting a 329 kb region of the chromosome spanning the origin of replication, resulted in allele replacement and loss or gain of an array of genes influencing host–pathogen interactions. Of note, molecular functional analyses revealed that the ST71 hybrid clone has acquired multiple novel pathogenic traits associated with acquired and innate immune evasion and bovine extracellular matrix adherence. These findings provide a paradigm for the impact of large-scale recombination events on the rapid evolution of bacterial pathogens within defined ecological niches.
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spelling pubmed-53206252017-03-27 Recombination-mediated remodelling of host–pathogen interactions during Staphylococcus aureus niche adaptation Spoor, Laura E. Richardson, Emily Richards, Amy C. Wilson, Gillian J. Mendonca, Chriselle Gupta, Ravi Kr. McAdam, Paul R. Nutbeam-Tuffs, Stephen Black, Nikki S. O'Gara, James P. Lee, Chia Y. Corander, Jukka Ross Fitzgerald, J. Microb Genom Research Paper Large-scale recombination events have led to the emergence of epidemic clones of several major bacterial pathogens. However, the functional impact of the recombination on clonal success is not understood. Here, we identified a novel widespread hybrid clone (ST71) of livestock-associated Staphylococcus aureus that evolved from an ancestor belonging to the major bovine lineage CC97, through multiple large-scale recombination events with other S. aureus lineages occupying the same ruminant niche. The recombination events, affecting a 329 kb region of the chromosome spanning the origin of replication, resulted in allele replacement and loss or gain of an array of genes influencing host–pathogen interactions. Of note, molecular functional analyses revealed that the ST71 hybrid clone has acquired multiple novel pathogenic traits associated with acquired and innate immune evasion and bovine extracellular matrix adherence. These findings provide a paradigm for the impact of large-scale recombination events on the rapid evolution of bacterial pathogens within defined ecological niches. Microbiology Society 2015-10-30 /pmc/articles/PMC5320625/ /pubmed/28348819 http://dx.doi.org/10.1099/mgen.0.000036 Text en © 2015 The Authors http://creativecommons.org/licenses/by/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Research Paper
Spoor, Laura E.
Richardson, Emily
Richards, Amy C.
Wilson, Gillian J.
Mendonca, Chriselle
Gupta, Ravi Kr.
McAdam, Paul R.
Nutbeam-Tuffs, Stephen
Black, Nikki S.
O'Gara, James P.
Lee, Chia Y.
Corander, Jukka
Ross Fitzgerald, J.
Recombination-mediated remodelling of host–pathogen interactions during Staphylococcus aureus niche adaptation
title Recombination-mediated remodelling of host–pathogen interactions during Staphylococcus aureus niche adaptation
title_full Recombination-mediated remodelling of host–pathogen interactions during Staphylococcus aureus niche adaptation
title_fullStr Recombination-mediated remodelling of host–pathogen interactions during Staphylococcus aureus niche adaptation
title_full_unstemmed Recombination-mediated remodelling of host–pathogen interactions during Staphylococcus aureus niche adaptation
title_short Recombination-mediated remodelling of host–pathogen interactions during Staphylococcus aureus niche adaptation
title_sort recombination-mediated remodelling of host–pathogen interactions during staphylococcus aureus niche adaptation
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5320625/
https://www.ncbi.nlm.nih.gov/pubmed/28348819
http://dx.doi.org/10.1099/mgen.0.000036
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