Disease-associated genotypes of the commensal skin bacterium Staphylococcus epidermidis
Some of the most common infectious diseases are caused by bacteria that naturally colonise humans asymptomatically. Combating these opportunistic pathogens requires an understanding of the traits that differentiate infecting strains from harmless relatives. Staphylococcus epidermidis is carried asym...
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th-cmuir.6653943832-629572018-12-14T04:10:15Z Disease-associated genotypes of the commensal skin bacterium Staphylococcus epidermidis Guillaume Méric Leonardos Mageiros Johan Pensar Maisem Laabei Koji Yahara Ben Pascoe Nattinee Kittiwan Phacharaporn Tadee Virginia Post Sarah Lamble Rory Bowden James E. Bray Mario Morgenstern Keith A. Jolley Martin C.J. Maiden Edward J. Feil Xavier Didelot Maria Miragaia Herminia de Lencastre T. Fintan Moriarty Holger Rohde Ruth Massey Dietrich Mack Jukka Corander Samuel K. Sheppard Biochemistry, Genetics and Molecular Biology Chemistry Physics and Astronomy Some of the most common infectious diseases are caused by bacteria that naturally colonise humans asymptomatically. Combating these opportunistic pathogens requires an understanding of the traits that differentiate infecting strains from harmless relatives. Staphylococcus epidermidis is carried asymptomatically on the skin and mucous membranes of virtually all humans but is a major cause of nosocomial infection associated with invasive procedures. Here we address the underlying evolutionary mechanisms of opportunistic pathogenicity by combining pangenome-wide association studies and laboratory microbiology to compare S. epidermidis from bloodstream and wound infections and asymptomatic carriage. We identify 61 genes containing infection-associated genetic elements (k-mers) that correlate with in vitro variation in known pathogenicity traits (biofilm formation, cell toxicity, interleukin-8 production, methicillin resistance). Horizontal gene transfer spreads these elements, allowing divergent clones to cause infection. Finally, Random Forest model prediction of disease status (carriage vs. infection) identifies pathogenicity elements in 415 S. epidermidis isolates with 80% accuracy, demonstrating the potential for identifying risk genotypes pre-operatively. 2018-12-14T03:46:03Z 2018-12-14T03:46:03Z 2018-11-28 Journal 20411723 2-s2.0-85057519497 10.1038/s41467-018-07368-7 https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85057519497&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/62957 |
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Biochemistry, Genetics and Molecular Biology Chemistry Physics and Astronomy Guillaume Méric Leonardos Mageiros Johan Pensar Maisem Laabei Koji Yahara Ben Pascoe Nattinee Kittiwan Phacharaporn Tadee Virginia Post Sarah Lamble Rory Bowden James E. Bray Mario Morgenstern Keith A. Jolley Martin C.J. Maiden Edward J. Feil Xavier Didelot Maria Miragaia Herminia de Lencastre T. Fintan Moriarty Holger Rohde Ruth Massey Dietrich Mack Jukka Corander Samuel K. Sheppard Disease-associated genotypes of the commensal skin bacterium Staphylococcus epidermidis |
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Some of the most common infectious diseases are caused by bacteria that naturally colonise humans asymptomatically. Combating these opportunistic pathogens requires an understanding of the traits that differentiate infecting strains from harmless relatives. Staphylococcus epidermidis is carried asymptomatically on the skin and mucous membranes of virtually all humans but is a major cause of nosocomial infection associated with invasive procedures. Here we address the underlying evolutionary mechanisms of opportunistic pathogenicity by combining pangenome-wide association studies and laboratory microbiology to compare S. epidermidis from bloodstream and wound infections and asymptomatic carriage. We identify 61 genes containing infection-associated genetic elements (k-mers) that correlate with in vitro variation in known pathogenicity traits (biofilm formation, cell toxicity, interleukin-8 production, methicillin resistance). Horizontal gene transfer spreads these elements, allowing divergent clones to cause infection. Finally, Random Forest model prediction of disease status (carriage vs. infection) identifies pathogenicity elements in 415 S. epidermidis isolates with 80% accuracy, demonstrating the potential for identifying risk genotypes pre-operatively. |
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author |
Guillaume Méric Leonardos Mageiros Johan Pensar Maisem Laabei Koji Yahara Ben Pascoe Nattinee Kittiwan Phacharaporn Tadee Virginia Post Sarah Lamble Rory Bowden James E. Bray Mario Morgenstern Keith A. Jolley Martin C.J. Maiden Edward J. Feil Xavier Didelot Maria Miragaia Herminia de Lencastre T. Fintan Moriarty Holger Rohde Ruth Massey Dietrich Mack Jukka Corander Samuel K. Sheppard |
author_facet |
Guillaume Méric Leonardos Mageiros Johan Pensar Maisem Laabei Koji Yahara Ben Pascoe Nattinee Kittiwan Phacharaporn Tadee Virginia Post Sarah Lamble Rory Bowden James E. Bray Mario Morgenstern Keith A. Jolley Martin C.J. Maiden Edward J. Feil Xavier Didelot Maria Miragaia Herminia de Lencastre T. Fintan Moriarty Holger Rohde Ruth Massey Dietrich Mack Jukka Corander Samuel K. Sheppard |
author_sort |
Guillaume Méric |
title |
Disease-associated genotypes of the commensal skin bacterium Staphylococcus epidermidis |
title_short |
Disease-associated genotypes of the commensal skin bacterium Staphylococcus epidermidis |
title_full |
Disease-associated genotypes of the commensal skin bacterium Staphylococcus epidermidis |
title_fullStr |
Disease-associated genotypes of the commensal skin bacterium Staphylococcus epidermidis |
title_full_unstemmed |
Disease-associated genotypes of the commensal skin bacterium Staphylococcus epidermidis |
title_sort |
disease-associated genotypes of the commensal skin bacterium staphylococcus epidermidis |
publishDate |
2018 |
url |
https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85057519497&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/62957 |
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1681425902859190272 |