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Longitudinal sampling of the lung microbiota in individuals with cystic fibrosis
Cystic fibrosis (CF) manifests in the lungs resulting in chronic microbial infection. Most morbidity and mortality in CF is due to cycles of pulmonary exacerbations—episodes of acute inflammation in response to the lung microbiome—which are difficult to prevent and treat because their cause is not w...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5333848/ https://www.ncbi.nlm.nih.gov/pubmed/28253277 http://dx.doi.org/10.1371/journal.pone.0172811 |
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author | Whelan, Fiona J. Heirali, Alya A. Rossi, Laura Rabin, Harvey R. Parkins, Michael D. Surette, Michael G. |
author_facet | Whelan, Fiona J. Heirali, Alya A. Rossi, Laura Rabin, Harvey R. Parkins, Michael D. Surette, Michael G. |
author_sort | Whelan, Fiona J. |
collection | PubMed |
description | Cystic fibrosis (CF) manifests in the lungs resulting in chronic microbial infection. Most morbidity and mortality in CF is due to cycles of pulmonary exacerbations—episodes of acute inflammation in response to the lung microbiome—which are difficult to prevent and treat because their cause is not well understood. We hypothesized that longitudinal analyses of the bacterial component of the CF lung microbiome may elucidate causative agents within this community for pulmonary exacerbations. In this study, 6 participants were sampled thrice-weekly for up to one year. During sampling, sputum, and data (antibiotic usage, spirometry, and symptom scores) were collected. Time points were categorized based on relation to exacerbation as Stable, Intermediate, and Treatment. Retrospectively, a subset of were interrogated via 16S rRNA gene sequencing. When samples were examined categorically, a significant difference between the lung microbiota in Stable, Intermediate, and Treatment samples was observed in a subset of participants. However, when samples were examined longitudinally, no correlations between microbial composition and collected data (antibiotic usage, spirometry, and symptom scores) were observed upon exacerbation onset. In this study, we identified no universal indicator within the lung microbiome of exacerbation onset but instead showed that changes to the CF lung microbiome occur outside of acute pulmonary episodes and are patient-specific. |
format | Online Article Text |
id | pubmed-5333848 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-53338482017-03-10 Longitudinal sampling of the lung microbiota in individuals with cystic fibrosis Whelan, Fiona J. Heirali, Alya A. Rossi, Laura Rabin, Harvey R. Parkins, Michael D. Surette, Michael G. PLoS One Research Article Cystic fibrosis (CF) manifests in the lungs resulting in chronic microbial infection. Most morbidity and mortality in CF is due to cycles of pulmonary exacerbations—episodes of acute inflammation in response to the lung microbiome—which are difficult to prevent and treat because their cause is not well understood. We hypothesized that longitudinal analyses of the bacterial component of the CF lung microbiome may elucidate causative agents within this community for pulmonary exacerbations. In this study, 6 participants were sampled thrice-weekly for up to one year. During sampling, sputum, and data (antibiotic usage, spirometry, and symptom scores) were collected. Time points were categorized based on relation to exacerbation as Stable, Intermediate, and Treatment. Retrospectively, a subset of were interrogated via 16S rRNA gene sequencing. When samples were examined categorically, a significant difference between the lung microbiota in Stable, Intermediate, and Treatment samples was observed in a subset of participants. However, when samples were examined longitudinally, no correlations between microbial composition and collected data (antibiotic usage, spirometry, and symptom scores) were observed upon exacerbation onset. In this study, we identified no universal indicator within the lung microbiome of exacerbation onset but instead showed that changes to the CF lung microbiome occur outside of acute pulmonary episodes and are patient-specific. Public Library of Science 2017-03-02 /pmc/articles/PMC5333848/ /pubmed/28253277 http://dx.doi.org/10.1371/journal.pone.0172811 Text en © 2017 Whelan 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 (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Whelan, Fiona J. Heirali, Alya A. Rossi, Laura Rabin, Harvey R. Parkins, Michael D. Surette, Michael G. Longitudinal sampling of the lung microbiota in individuals with cystic fibrosis |
title | Longitudinal sampling of the lung microbiota in individuals with cystic fibrosis |
title_full | Longitudinal sampling of the lung microbiota in individuals with cystic fibrosis |
title_fullStr | Longitudinal sampling of the lung microbiota in individuals with cystic fibrosis |
title_full_unstemmed | Longitudinal sampling of the lung microbiota in individuals with cystic fibrosis |
title_short | Longitudinal sampling of the lung microbiota in individuals with cystic fibrosis |
title_sort | longitudinal sampling of the lung microbiota in individuals with cystic fibrosis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5333848/ https://www.ncbi.nlm.nih.gov/pubmed/28253277 http://dx.doi.org/10.1371/journal.pone.0172811 |
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