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Propionibacterium acnes strain populations in the human skin microbiome associated with acne
The human skin microbiome plays important roles in skin health and disease. However, bacterial population structure and diversity at the strain level is poorly understood. We compared the skin microbiome at the strain level and genome level of Propionibacterium acnes, a dominant skin commensal, betw...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3745799/ https://www.ncbi.nlm.nih.gov/pubmed/23337890 http://dx.doi.org/10.1038/jid.2013.21 |
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author | Fitz-Gibbon, Sorel Tomida, Shuta Chiu, Bor-Han Nguyen, Lin Du, Christine Liu, Minghsun Elashoff, David Erfe, Marie C. Loncaric, Anya Kim, Jenny Modlin, Robert L. Miller, Jeff F. Sodergren, Erica Craft, Noah Weinstock, George M. Li, Huiying |
author_facet | Fitz-Gibbon, Sorel Tomida, Shuta Chiu, Bor-Han Nguyen, Lin Du, Christine Liu, Minghsun Elashoff, David Erfe, Marie C. Loncaric, Anya Kim, Jenny Modlin, Robert L. Miller, Jeff F. Sodergren, Erica Craft, Noah Weinstock, George M. Li, Huiying |
author_sort | Fitz-Gibbon, Sorel |
collection | PubMed |
description | The human skin microbiome plays important roles in skin health and disease. However, bacterial population structure and diversity at the strain level is poorly understood. We compared the skin microbiome at the strain level and genome level of Propionibacterium acnes, a dominant skin commensal, between 49 acne patients and 52 healthy individuals by sampling the pilosebaceous units on their noses. Metagenomic analysis demonstrated that while the relative abundances of P. acnes were similar, the strain population structures were significantly different in the two cohorts. Certain strains were highly associated with acne and other strains were enriched in healthy skin. By sequencing 66 previously unreported P. acnes strains and comparing 71 P. acnes genomes, we identified potential genetic determinants of various P. acnes strains in association with acne or health. Our analysis suggests that acquired DNA sequences and bacterial immune elements may play roles in determining virulence properties of P. acnes strains and some could be future targets for therapeutic interventions. This study demonstrates a previously unreported paradigm of commensal strain populations that could explain the pathogenesis of human diseases. It underscores the importance of strain level analysis of the human microbiome to define the role of commensals in health and disease. |
format | Online Article Text |
id | pubmed-3745799 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
record_format | MEDLINE/PubMed |
spelling | pubmed-37457992014-03-01 Propionibacterium acnes strain populations in the human skin microbiome associated with acne Fitz-Gibbon, Sorel Tomida, Shuta Chiu, Bor-Han Nguyen, Lin Du, Christine Liu, Minghsun Elashoff, David Erfe, Marie C. Loncaric, Anya Kim, Jenny Modlin, Robert L. Miller, Jeff F. Sodergren, Erica Craft, Noah Weinstock, George M. Li, Huiying J Invest Dermatol Article The human skin microbiome plays important roles in skin health and disease. However, bacterial population structure and diversity at the strain level is poorly understood. We compared the skin microbiome at the strain level and genome level of Propionibacterium acnes, a dominant skin commensal, between 49 acne patients and 52 healthy individuals by sampling the pilosebaceous units on their noses. Metagenomic analysis demonstrated that while the relative abundances of P. acnes were similar, the strain population structures were significantly different in the two cohorts. Certain strains were highly associated with acne and other strains were enriched in healthy skin. By sequencing 66 previously unreported P. acnes strains and comparing 71 P. acnes genomes, we identified potential genetic determinants of various P. acnes strains in association with acne or health. Our analysis suggests that acquired DNA sequences and bacterial immune elements may play roles in determining virulence properties of P. acnes strains and some could be future targets for therapeutic interventions. This study demonstrates a previously unreported paradigm of commensal strain populations that could explain the pathogenesis of human diseases. It underscores the importance of strain level analysis of the human microbiome to define the role of commensals in health and disease. 2013-01-21 2013-09 /pmc/articles/PMC3745799/ /pubmed/23337890 http://dx.doi.org/10.1038/jid.2013.21 Text en http://www.nature.com/authors/editorial_policies/license.html#terms Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article Fitz-Gibbon, Sorel Tomida, Shuta Chiu, Bor-Han Nguyen, Lin Du, Christine Liu, Minghsun Elashoff, David Erfe, Marie C. Loncaric, Anya Kim, Jenny Modlin, Robert L. Miller, Jeff F. Sodergren, Erica Craft, Noah Weinstock, George M. Li, Huiying Propionibacterium acnes strain populations in the human skin microbiome associated with acne |
title | Propionibacterium acnes strain populations in the
human skin microbiome associated with acne |
title_full | Propionibacterium acnes strain populations in the
human skin microbiome associated with acne |
title_fullStr | Propionibacterium acnes strain populations in the
human skin microbiome associated with acne |
title_full_unstemmed | Propionibacterium acnes strain populations in the
human skin microbiome associated with acne |
title_short | Propionibacterium acnes strain populations in the
human skin microbiome associated with acne |
title_sort | propionibacterium acnes strain populations in the
human skin microbiome associated with acne |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3745799/ https://www.ncbi.nlm.nih.gov/pubmed/23337890 http://dx.doi.org/10.1038/jid.2013.21 |
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