Airway microbiota and pathogen abundance in age-stratified cystic fibrosis patients.

Bacterial communities in the airways of cystic fibrosis (CF) patients are, as in other ecological niches, influenced by autogenic and allogenic factors. However, our understanding of microbial colonization in younger versus older CF airways and the association with pulmonary function is rudimentary...

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Autores principales: Michael J Cox, Martin Allgaier, Byron Taylor, Marshall S Baek, Yvonne J Huang, Rebecca A Daly, Ulas Karaoz, Gary L Andersen, Ronald Brown, Kei E Fujimura, Brian Wu, Diem Tran, Jonathan Koff, Mary Ellen Kleinhenz, Dennis Nielson, Eoin L Brodie, Susan V Lynch
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Publicado: Public Library of Science (PLoS) 2010
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spelling oai:doaj.org-article:b72a83e3d7364745afd34bb63d9b865f2021-12-02T20:20:35ZAirway microbiota and pathogen abundance in age-stratified cystic fibrosis patients.1932-620310.1371/journal.pone.0011044https://doaj.org/article/b72a83e3d7364745afd34bb63d9b865f2010-06-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/20585638/?tool=EBIhttps://doaj.org/toc/1932-6203Bacterial communities in the airways of cystic fibrosis (CF) patients are, as in other ecological niches, influenced by autogenic and allogenic factors. However, our understanding of microbial colonization in younger versus older CF airways and the association with pulmonary function is rudimentary at best. Using a phylogenetic microarray, we examine the airway microbiota in age stratified CF patients ranging from neonates (9 months) to adults (72 years). From a cohort of clinically stable patients, we demonstrate that older CF patients who exhibit poorer pulmonary function possess more uneven, phylogenetically-clustered airway communities, compared to younger patients. Using longitudinal samples collected form a subset of these patients a pattern of initial bacterial community diversification was observed in younger patients compared with a progressive loss of diversity over time in older patients. We describe in detail the distinct bacterial community profiles associated with young and old CF patients with a particular focus on the differences between respective "early" and "late" colonizing organisms. Finally we assess the influence of Cystic Fibrosis Transmembrane Regulator (CFTR) mutation on bacterial abundance and identify genotype-specific communities involving members of the Pseudomonadaceae, Xanthomonadaceae, Moraxellaceae and Enterobacteriaceae amongst others. Data presented here provides insights into the CF airway microbiota, including initial diversification events in younger patients and establishment of specialized communities of pathogens associated with poor pulmonary function in older patient populations.Michael J CoxMartin AllgaierByron TaylorMarshall S BaekYvonne J HuangRebecca A DalyUlas KaraozGary L AndersenRonald BrownKei E FujimuraBrian WuDiem TranJonathan KoffMary Ellen KleinhenzDennis NielsonEoin L BrodieSusan V LynchPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 5, Iss 6, p e11044 (2010)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Michael J Cox
Martin Allgaier
Byron Taylor
Marshall S Baek
Yvonne J Huang
Rebecca A Daly
Ulas Karaoz
Gary L Andersen
Ronald Brown
Kei E Fujimura
Brian Wu
Diem Tran
Jonathan Koff
Mary Ellen Kleinhenz
Dennis Nielson
Eoin L Brodie
Susan V Lynch
Airway microbiota and pathogen abundance in age-stratified cystic fibrosis patients.
description Bacterial communities in the airways of cystic fibrosis (CF) patients are, as in other ecological niches, influenced by autogenic and allogenic factors. However, our understanding of microbial colonization in younger versus older CF airways and the association with pulmonary function is rudimentary at best. Using a phylogenetic microarray, we examine the airway microbiota in age stratified CF patients ranging from neonates (9 months) to adults (72 years). From a cohort of clinically stable patients, we demonstrate that older CF patients who exhibit poorer pulmonary function possess more uneven, phylogenetically-clustered airway communities, compared to younger patients. Using longitudinal samples collected form a subset of these patients a pattern of initial bacterial community diversification was observed in younger patients compared with a progressive loss of diversity over time in older patients. We describe in detail the distinct bacterial community profiles associated with young and old CF patients with a particular focus on the differences between respective "early" and "late" colonizing organisms. Finally we assess the influence of Cystic Fibrosis Transmembrane Regulator (CFTR) mutation on bacterial abundance and identify genotype-specific communities involving members of the Pseudomonadaceae, Xanthomonadaceae, Moraxellaceae and Enterobacteriaceae amongst others. Data presented here provides insights into the CF airway microbiota, including initial diversification events in younger patients and establishment of specialized communities of pathogens associated with poor pulmonary function in older patient populations.
format article
author Michael J Cox
Martin Allgaier
Byron Taylor
Marshall S Baek
Yvonne J Huang
Rebecca A Daly
Ulas Karaoz
Gary L Andersen
Ronald Brown
Kei E Fujimura
Brian Wu
Diem Tran
Jonathan Koff
Mary Ellen Kleinhenz
Dennis Nielson
Eoin L Brodie
Susan V Lynch
author_facet Michael J Cox
Martin Allgaier
Byron Taylor
Marshall S Baek
Yvonne J Huang
Rebecca A Daly
Ulas Karaoz
Gary L Andersen
Ronald Brown
Kei E Fujimura
Brian Wu
Diem Tran
Jonathan Koff
Mary Ellen Kleinhenz
Dennis Nielson
Eoin L Brodie
Susan V Lynch
author_sort Michael J Cox
title Airway microbiota and pathogen abundance in age-stratified cystic fibrosis patients.
title_short Airway microbiota and pathogen abundance in age-stratified cystic fibrosis patients.
title_full Airway microbiota and pathogen abundance in age-stratified cystic fibrosis patients.
title_fullStr Airway microbiota and pathogen abundance in age-stratified cystic fibrosis patients.
title_full_unstemmed Airway microbiota and pathogen abundance in age-stratified cystic fibrosis patients.
title_sort airway microbiota and pathogen abundance in age-stratified cystic fibrosis patients.
publisher Public Library of Science (PLoS)
publishDate 2010
url https://doaj.org/article/b72a83e3d7364745afd34bb63d9b865f
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