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The Human Nasal Microbiota and Staphylococcus aureus Carriage

BACKGROUND: Colonization of humans with Staphylococcus aureus is a critical prerequisite of subsequent clinical infection of the skin, blood, lung, heart and other deep tissues. S. aureus persistently or intermittently colonizes the nares of ∼50% of healthy adults, whereas ∼50% of the general popula...

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Autores principales: Frank, Daniel N., Feazel, Leah M., Bessesen, Mary T., Price, Connie S., Janoff, Edward N., Pace, Norman R.
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2871794/
https://www.ncbi.nlm.nih.gov/pubmed/20498722
http://dx.doi.org/10.1371/journal.pone.0010598
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author Frank, Daniel N.
Feazel, Leah M.
Bessesen, Mary T.
Price, Connie S.
Janoff, Edward N.
Pace, Norman R.
author_facet Frank, Daniel N.
Feazel, Leah M.
Bessesen, Mary T.
Price, Connie S.
Janoff, Edward N.
Pace, Norman R.
author_sort Frank, Daniel N.
collection PubMed
description BACKGROUND: Colonization of humans with Staphylococcus aureus is a critical prerequisite of subsequent clinical infection of the skin, blood, lung, heart and other deep tissues. S. aureus persistently or intermittently colonizes the nares of ∼50% of healthy adults, whereas ∼50% of the general population is rarely or never colonized by this pathogen. Because microbial consortia within the nasal cavity may be an important determinant of S. aureus colonization we determined the composition and dynamics of the nasal microbiota and correlated specific microorganisms with S. aureus colonization. METHODOLOGY/PRINCIPAL FINDINGS: Nasal specimens were collected longitudinally from five healthy adults and a cross-section of hospitalized patients (26 S. aureus carriers and 16 non-carriers). Culture-independent analysis of 16S rRNA sequences revealed that the nasal microbiota of healthy subjects consists primarily of members of the phylum Actinobacteria (e.g., Propionibacterium spp. and Corynebacterium spp.), with proportionally less representation of other phyla, including Firmicutes (e.g., Staphylococcus spp.) and Proteobacteria (e.g. Enterobacter spp). In contrast, inpatient nasal microbiotas were enriched in S. aureus or Staphylococcus epidermidis and diminished in several actinobacterial groups, most notably Propionibacterium acnes. Moreover, within the inpatient population S. aureus colonization was negatively correlated with the abundances of several microbial groups, including S. epidermidis (p = 0.004). CONCLUSIONS/SIGNIFICANCE: The nares environment is colonized by a temporally stable microbiota that is distinct from other regions of the integument. Negative association between S. aureus, S. epidermidis, and other groups suggests microbial competition during colonization of the nares, a finding that could be exploited to limit S. aureus colonization.
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spelling pubmed-28717942010-05-24 The Human Nasal Microbiota and Staphylococcus aureus Carriage Frank, Daniel N. Feazel, Leah M. Bessesen, Mary T. Price, Connie S. Janoff, Edward N. Pace, Norman R. PLoS One Research Article BACKGROUND: Colonization of humans with Staphylococcus aureus is a critical prerequisite of subsequent clinical infection of the skin, blood, lung, heart and other deep tissues. S. aureus persistently or intermittently colonizes the nares of ∼50% of healthy adults, whereas ∼50% of the general population is rarely or never colonized by this pathogen. Because microbial consortia within the nasal cavity may be an important determinant of S. aureus colonization we determined the composition and dynamics of the nasal microbiota and correlated specific microorganisms with S. aureus colonization. METHODOLOGY/PRINCIPAL FINDINGS: Nasal specimens were collected longitudinally from five healthy adults and a cross-section of hospitalized patients (26 S. aureus carriers and 16 non-carriers). Culture-independent analysis of 16S rRNA sequences revealed that the nasal microbiota of healthy subjects consists primarily of members of the phylum Actinobacteria (e.g., Propionibacterium spp. and Corynebacterium spp.), with proportionally less representation of other phyla, including Firmicutes (e.g., Staphylococcus spp.) and Proteobacteria (e.g. Enterobacter spp). In contrast, inpatient nasal microbiotas were enriched in S. aureus or Staphylococcus epidermidis and diminished in several actinobacterial groups, most notably Propionibacterium acnes. Moreover, within the inpatient population S. aureus colonization was negatively correlated with the abundances of several microbial groups, including S. epidermidis (p = 0.004). CONCLUSIONS/SIGNIFICANCE: The nares environment is colonized by a temporally stable microbiota that is distinct from other regions of the integument. Negative association between S. aureus, S. epidermidis, and other groups suggests microbial competition during colonization of the nares, a finding that could be exploited to limit S. aureus colonization. Public Library of Science 2010-05-17 /pmc/articles/PMC2871794/ /pubmed/20498722 http://dx.doi.org/10.1371/journal.pone.0010598 Text en Frank et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Frank, Daniel N.
Feazel, Leah M.
Bessesen, Mary T.
Price, Connie S.
Janoff, Edward N.
Pace, Norman R.
The Human Nasal Microbiota and Staphylococcus aureus Carriage
title The Human Nasal Microbiota and Staphylococcus aureus Carriage
title_full The Human Nasal Microbiota and Staphylococcus aureus Carriage
title_fullStr The Human Nasal Microbiota and Staphylococcus aureus Carriage
title_full_unstemmed The Human Nasal Microbiota and Staphylococcus aureus Carriage
title_short The Human Nasal Microbiota and Staphylococcus aureus Carriage
title_sort human nasal microbiota and staphylococcus aureus carriage
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2871794/
https://www.ncbi.nlm.nih.gov/pubmed/20498722
http://dx.doi.org/10.1371/journal.pone.0010598
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