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Microbiome networks and change-point analysis reveal key community changes associated with cystic fibrosis pulmonary exacerbations
Over 90% of cystic fibrosis (CF) patients die due to chronic lung infections leading to respiratory failure. The decline in CF lung function is greatly accelerated by intermittent and progressively severe acute pulmonary exacerbations (PEs). Despite their clinical impact, surprisingly few microbiolo...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6341074/ https://www.ncbi.nlm.nih.gov/pubmed/30675371 http://dx.doi.org/10.1038/s41522-018-0077-y |
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author | Layeghifard, Mehdi Li, Hannah Wang, Pauline W. Donaldson, Sylva L. Coburn, Bryan Clark, Shawn T. Caballero, Julio Diaz Zhang, Yu Tullis, D. Elizabeth Yau, Yvonne C. W. Waters, Valerie Hwang, David M. Guttman, David S. |
author_facet | Layeghifard, Mehdi Li, Hannah Wang, Pauline W. Donaldson, Sylva L. Coburn, Bryan Clark, Shawn T. Caballero, Julio Diaz Zhang, Yu Tullis, D. Elizabeth Yau, Yvonne C. W. Waters, Valerie Hwang, David M. Guttman, David S. |
author_sort | Layeghifard, Mehdi |
collection | PubMed |
description | Over 90% of cystic fibrosis (CF) patients die due to chronic lung infections leading to respiratory failure. The decline in CF lung function is greatly accelerated by intermittent and progressively severe acute pulmonary exacerbations (PEs). Despite their clinical impact, surprisingly few microbiological signals associated with PEs have been identified. Here we introduce an unsupervised, systems-oriented approach to identify key members of the microbiota. We used two CF sputum microbiome data sets that were longitudinally collected through periods spanning baseline health and PEs. Key taxa were defined based on three strategies: overall relative abundance, prevalence, and co-occurrence network interconnectedness. We measured the association between changes in the abundance of the key taxa and changes in patient clinical status over time via change-point detection, and found that taxa with the highest level of network interconnectedness tracked changes in patient health significantly better than taxa with the highest abundance or prevalence. We also cross-sectionally stratified all samples into the clinical states and identified key taxa associated with each state. We found that network interconnectedness most strongly delineated the taxa among clinical states, and that anaerobic bacteria were over-represented during PEs. Many of these anaerobes are oropharyngeal bacteria that have been previously isolated from the respiratory tract, and/or have been studied for their role in CF. The observed shift in community structure, and the association of anaerobic taxa and PEs lends further support to the growing consensus that anoxic conditions and the subsequent growth of anaerobic microbes are important predictors of PEs. |
format | Online Article Text |
id | pubmed-6341074 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-63410742019-01-23 Microbiome networks and change-point analysis reveal key community changes associated with cystic fibrosis pulmonary exacerbations Layeghifard, Mehdi Li, Hannah Wang, Pauline W. Donaldson, Sylva L. Coburn, Bryan Clark, Shawn T. Caballero, Julio Diaz Zhang, Yu Tullis, D. Elizabeth Yau, Yvonne C. W. Waters, Valerie Hwang, David M. Guttman, David S. NPJ Biofilms Microbiomes Article Over 90% of cystic fibrosis (CF) patients die due to chronic lung infections leading to respiratory failure. The decline in CF lung function is greatly accelerated by intermittent and progressively severe acute pulmonary exacerbations (PEs). Despite their clinical impact, surprisingly few microbiological signals associated with PEs have been identified. Here we introduce an unsupervised, systems-oriented approach to identify key members of the microbiota. We used two CF sputum microbiome data sets that were longitudinally collected through periods spanning baseline health and PEs. Key taxa were defined based on three strategies: overall relative abundance, prevalence, and co-occurrence network interconnectedness. We measured the association between changes in the abundance of the key taxa and changes in patient clinical status over time via change-point detection, and found that taxa with the highest level of network interconnectedness tracked changes in patient health significantly better than taxa with the highest abundance or prevalence. We also cross-sectionally stratified all samples into the clinical states and identified key taxa associated with each state. We found that network interconnectedness most strongly delineated the taxa among clinical states, and that anaerobic bacteria were over-represented during PEs. Many of these anaerobes are oropharyngeal bacteria that have been previously isolated from the respiratory tract, and/or have been studied for their role in CF. The observed shift in community structure, and the association of anaerobic taxa and PEs lends further support to the growing consensus that anoxic conditions and the subsequent growth of anaerobic microbes are important predictors of PEs. Nature Publishing Group UK 2019-01-21 /pmc/articles/PMC6341074/ /pubmed/30675371 http://dx.doi.org/10.1038/s41522-018-0077-y Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Layeghifard, Mehdi Li, Hannah Wang, Pauline W. Donaldson, Sylva L. Coburn, Bryan Clark, Shawn T. Caballero, Julio Diaz Zhang, Yu Tullis, D. Elizabeth Yau, Yvonne C. W. Waters, Valerie Hwang, David M. Guttman, David S. Microbiome networks and change-point analysis reveal key community changes associated with cystic fibrosis pulmonary exacerbations |
title | Microbiome networks and change-point analysis reveal key community changes associated with cystic fibrosis pulmonary exacerbations |
title_full | Microbiome networks and change-point analysis reveal key community changes associated with cystic fibrosis pulmonary exacerbations |
title_fullStr | Microbiome networks and change-point analysis reveal key community changes associated with cystic fibrosis pulmonary exacerbations |
title_full_unstemmed | Microbiome networks and change-point analysis reveal key community changes associated with cystic fibrosis pulmonary exacerbations |
title_short | Microbiome networks and change-point analysis reveal key community changes associated with cystic fibrosis pulmonary exacerbations |
title_sort | microbiome networks and change-point analysis reveal key community changes associated with cystic fibrosis pulmonary exacerbations |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6341074/ https://www.ncbi.nlm.nih.gov/pubmed/30675371 http://dx.doi.org/10.1038/s41522-018-0077-y |
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