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Profiling bacterial community in upper respiratory tracts

BACKGROUND: Infection by pathogenic viruses results in rapid epithelial damage and significantly impacts on the condition of the upper respiratory tract, thus the effects of viral infection may induce changes in microbiota. Thus, we aimed to define the healthy microbiota and the viral pathogen-affec...

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Autores principales: Yi, Hana, Yong, Dongeun, Lee, Kyungwon, Cho, Yong-Joon, Chun, Jongsik
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4236460/
https://www.ncbi.nlm.nih.gov/pubmed/25391813
http://dx.doi.org/10.1186/s12879-014-0583-3
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author Yi, Hana
Yong, Dongeun
Lee, Kyungwon
Cho, Yong-Joon
Chun, Jongsik
author_facet Yi, Hana
Yong, Dongeun
Lee, Kyungwon
Cho, Yong-Joon
Chun, Jongsik
author_sort Yi, Hana
collection PubMed
description BACKGROUND: Infection by pathogenic viruses results in rapid epithelial damage and significantly impacts on the condition of the upper respiratory tract, thus the effects of viral infection may induce changes in microbiota. Thus, we aimed to define the healthy microbiota and the viral pathogen-affected microbiota in the upper respiratory tract. In addition, any association between the type of viral agent and the resultant microbiota profile was assessed. METHODS: We analyzed the upper respiratory tract bacterial content of 57 healthy asymptomatic people (17 health-care workers and 40 community people) and 59 patients acutely infected with influenza, parainfluenza, rhino, respiratory syncytial, corona, adeno, or metapneumo viruses using culture-independent pyrosequencing. RESULTS: The healthy subjects harbored primarily Streptococcus, whereas the patients showed an enrichment of Haemophilus or Moraxella. Quantifying the similarities between bacterial populations by using Fast UniFrac analysis indicated that bacterial profiles were apparently divisible into 6 oropharyngeal types in the tested subjects. The oropharyngeal types were not associated with the type of viruses, but were rather linked to the age of the subjects. Moraxella nonliquefaciens exhibited unprecedentedly high abundance in young subjects aged <6 years. The genome of M. nonliquefaciens was found to encode various proteins that may play roles in pathogenesis. CONCLUSIONS: This study identified 6 oropharyngeal microbiome types. No virus-specific bacterial profile was discovered, but comparative analysis of healthy adults and patients identified a bacterium specific to young patients, M. nonliquefaciens. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12879-014-0583-3) contains supplementary material, which is available to authorized users.
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spelling pubmed-42364602014-11-19 Profiling bacterial community in upper respiratory tracts Yi, Hana Yong, Dongeun Lee, Kyungwon Cho, Yong-Joon Chun, Jongsik BMC Infect Dis Research Article BACKGROUND: Infection by pathogenic viruses results in rapid epithelial damage and significantly impacts on the condition of the upper respiratory tract, thus the effects of viral infection may induce changes in microbiota. Thus, we aimed to define the healthy microbiota and the viral pathogen-affected microbiota in the upper respiratory tract. In addition, any association between the type of viral agent and the resultant microbiota profile was assessed. METHODS: We analyzed the upper respiratory tract bacterial content of 57 healthy asymptomatic people (17 health-care workers and 40 community people) and 59 patients acutely infected with influenza, parainfluenza, rhino, respiratory syncytial, corona, adeno, or metapneumo viruses using culture-independent pyrosequencing. RESULTS: The healthy subjects harbored primarily Streptococcus, whereas the patients showed an enrichment of Haemophilus or Moraxella. Quantifying the similarities between bacterial populations by using Fast UniFrac analysis indicated that bacterial profiles were apparently divisible into 6 oropharyngeal types in the tested subjects. The oropharyngeal types were not associated with the type of viruses, but were rather linked to the age of the subjects. Moraxella nonliquefaciens exhibited unprecedentedly high abundance in young subjects aged <6 years. The genome of M. nonliquefaciens was found to encode various proteins that may play roles in pathogenesis. CONCLUSIONS: This study identified 6 oropharyngeal microbiome types. No virus-specific bacterial profile was discovered, but comparative analysis of healthy adults and patients identified a bacterium specific to young patients, M. nonliquefaciens. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12879-014-0583-3) contains supplementary material, which is available to authorized users. BioMed Central 2014-11-13 /pmc/articles/PMC4236460/ /pubmed/25391813 http://dx.doi.org/10.1186/s12879-014-0583-3 Text en © Yi et al.; licensee BioMed Central Ltd. 2014 This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Yi, Hana
Yong, Dongeun
Lee, Kyungwon
Cho, Yong-Joon
Chun, Jongsik
Profiling bacterial community in upper respiratory tracts
title Profiling bacterial community in upper respiratory tracts
title_full Profiling bacterial community in upper respiratory tracts
title_fullStr Profiling bacterial community in upper respiratory tracts
title_full_unstemmed Profiling bacterial community in upper respiratory tracts
title_short Profiling bacterial community in upper respiratory tracts
title_sort profiling bacterial community in upper respiratory tracts
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4236460/
https://www.ncbi.nlm.nih.gov/pubmed/25391813
http://dx.doi.org/10.1186/s12879-014-0583-3
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