The lung microbiome in moderate and severe chronic obstructive pulmonary disease.

Chronic obstructive pulmonary disease (COPD) is an inflammatory disorder characterized by incompletely reversible airflow obstruction. Bacterial infection of the lower respiratory tract contributes to approximately 50% of COPD exacerbations. Even during periods of stable lung function, the lung harb...

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Main Authors: Alexa A Pragman, Hyeun Bum Kim, Cavan S Reilly, Christine Wendt, Richard E Isaacson
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2012-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3469539?pdf=render
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spelling doaj-0f8535959ef045bbbdf93fb605cdb9e42020-11-25T01:19:59ZengPublic Library of Science (PLoS)PLoS ONE1932-62032012-01-01710e4730510.1371/journal.pone.0047305The lung microbiome in moderate and severe chronic obstructive pulmonary disease.Alexa A PragmanHyeun Bum KimCavan S ReillyChristine WendtRichard E IsaacsonChronic obstructive pulmonary disease (COPD) is an inflammatory disorder characterized by incompletely reversible airflow obstruction. Bacterial infection of the lower respiratory tract contributes to approximately 50% of COPD exacerbations. Even during periods of stable lung function, the lung harbors a community of bacteria, termed the microbiome. The role of the lung microbiome in the pathogenesis of COPD remains unknown. The COPD lung microbiome, like the healthy lung microbiome, appears to reflect microaspiration of oral microflora. Here we describe the COPD lung microbiome of 22 patients with Moderate or Severe COPD compared to 10 healthy control patients. The composition of the lung microbiomes was determined using 454 pyrosequencing of 16S rDNA found in bronchoalveolar lavage fluid. Sequences were analyzed using mothur, Ribosomal Database Project, Fast UniFrac, and Metastats. Our results showed a significant increase in microbial diversity with the development of COPD. The main phyla in all samples were Actinobacteria, Firmicutes, and Proteobacteria. Principal coordinate analyses demonstrated separation of control and COPD samples, but samples did not cluster based on disease severity. However, samples did cluster based on the use of inhaled corticosteroids and inhaled bronchodilators. Metastats analyses demonstrated an increased abundance of several oral bacteria in COPD samples.http://europepmc.org/articles/PMC3469539?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Alexa A Pragman
Hyeun Bum Kim
Cavan S Reilly
Christine Wendt
Richard E Isaacson
spellingShingle Alexa A Pragman
Hyeun Bum Kim
Cavan S Reilly
Christine Wendt
Richard E Isaacson
The lung microbiome in moderate and severe chronic obstructive pulmonary disease.
PLoS ONE
author_facet Alexa A Pragman
Hyeun Bum Kim
Cavan S Reilly
Christine Wendt
Richard E Isaacson
author_sort Alexa A Pragman
title The lung microbiome in moderate and severe chronic obstructive pulmonary disease.
title_short The lung microbiome in moderate and severe chronic obstructive pulmonary disease.
title_full The lung microbiome in moderate and severe chronic obstructive pulmonary disease.
title_fullStr The lung microbiome in moderate and severe chronic obstructive pulmonary disease.
title_full_unstemmed The lung microbiome in moderate and severe chronic obstructive pulmonary disease.
title_sort lung microbiome in moderate and severe chronic obstructive pulmonary disease.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2012-01-01
description Chronic obstructive pulmonary disease (COPD) is an inflammatory disorder characterized by incompletely reversible airflow obstruction. Bacterial infection of the lower respiratory tract contributes to approximately 50% of COPD exacerbations. Even during periods of stable lung function, the lung harbors a community of bacteria, termed the microbiome. The role of the lung microbiome in the pathogenesis of COPD remains unknown. The COPD lung microbiome, like the healthy lung microbiome, appears to reflect microaspiration of oral microflora. Here we describe the COPD lung microbiome of 22 patients with Moderate or Severe COPD compared to 10 healthy control patients. The composition of the lung microbiomes was determined using 454 pyrosequencing of 16S rDNA found in bronchoalveolar lavage fluid. Sequences were analyzed using mothur, Ribosomal Database Project, Fast UniFrac, and Metastats. Our results showed a significant increase in microbial diversity with the development of COPD. The main phyla in all samples were Actinobacteria, Firmicutes, and Proteobacteria. Principal coordinate analyses demonstrated separation of control and COPD samples, but samples did not cluster based on disease severity. However, samples did cluster based on the use of inhaled corticosteroids and inhaled bronchodilators. Metastats analyses demonstrated an increased abundance of several oral bacteria in COPD samples.
url http://europepmc.org/articles/PMC3469539?pdf=render
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