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The cystic fibrosis lower airways microbial metagenome
Chronic airway infections determine most morbidity in people with cystic fibrosis (CF). Herein, we present unbiased quantitative data about the frequency and abundance of DNA viruses, archaea, bacteria, moulds and fungi in CF lower airways. Induced sputa were collected on several occasions from chil...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
European Respiratory Society
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5005179/ https://www.ncbi.nlm.nih.gov/pubmed/27730195 http://dx.doi.org/10.1183/23120541.00096-2015 |
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author | Moran Losada, Patricia Chouvarine, Philippe Dorda, Marie Hedtfeld, Silke Mielke, Samira Schulz, Angela Wiehlmann, Lutz Tümmler, Burkhard |
author_facet | Moran Losada, Patricia Chouvarine, Philippe Dorda, Marie Hedtfeld, Silke Mielke, Samira Schulz, Angela Wiehlmann, Lutz Tümmler, Burkhard |
author_sort | Moran Losada, Patricia |
collection | PubMed |
description | Chronic airway infections determine most morbidity in people with cystic fibrosis (CF). Herein, we present unbiased quantitative data about the frequency and abundance of DNA viruses, archaea, bacteria, moulds and fungi in CF lower airways. Induced sputa were collected on several occasions from children, adolescents and adults with CF. Deep sputum metagenome sequencing identified, on average, approximately 10 DNA viruses or fungi and several hundred bacterial taxa. The metagenome of a CF patient was typically found to be made up of an individual signature of multiple, lowly abundant species superimposed by few disease-associated pathogens, such as Pseudomonas aeruginosa and Staphylococcus aureus, as major components. The host-associated signatures ranged from inconspicuous polymicrobial communities in healthy subjects to low-complexity microbiomes dominated by the typical CF pathogens in patients with advanced lung disease. The DNA virus community in CF lungs mainly consisted of phages and occasionally of human pathogens, such as adeno- and herpesviruses. The S. aureus and P. aeruginosa populations were composed of one major and numerous minor clone types. The rare clones constitute a low copy genetic resource that could rapidly expand as a response to habitat alterations, such as antimicrobial chemotherapy or invasion of novel microbes. |
format | Online Article Text |
id | pubmed-5005179 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | European Respiratory Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-50051792016-10-11 The cystic fibrosis lower airways microbial metagenome Moran Losada, Patricia Chouvarine, Philippe Dorda, Marie Hedtfeld, Silke Mielke, Samira Schulz, Angela Wiehlmann, Lutz Tümmler, Burkhard ERJ Open Res Original Articles Chronic airway infections determine most morbidity in people with cystic fibrosis (CF). Herein, we present unbiased quantitative data about the frequency and abundance of DNA viruses, archaea, bacteria, moulds and fungi in CF lower airways. Induced sputa were collected on several occasions from children, adolescents and adults with CF. Deep sputum metagenome sequencing identified, on average, approximately 10 DNA viruses or fungi and several hundred bacterial taxa. The metagenome of a CF patient was typically found to be made up of an individual signature of multiple, lowly abundant species superimposed by few disease-associated pathogens, such as Pseudomonas aeruginosa and Staphylococcus aureus, as major components. The host-associated signatures ranged from inconspicuous polymicrobial communities in healthy subjects to low-complexity microbiomes dominated by the typical CF pathogens in patients with advanced lung disease. The DNA virus community in CF lungs mainly consisted of phages and occasionally of human pathogens, such as adeno- and herpesviruses. The S. aureus and P. aeruginosa populations were composed of one major and numerous minor clone types. The rare clones constitute a low copy genetic resource that could rapidly expand as a response to habitat alterations, such as antimicrobial chemotherapy or invasion of novel microbes. European Respiratory Society 2016-05-09 /pmc/articles/PMC5005179/ /pubmed/27730195 http://dx.doi.org/10.1183/23120541.00096-2015 Text en Copyright ©ERS 2016 http://creativecommons.org/licenses/by-nc/4.0/ This article is open access and distributed under the terms of the Creative Commons Attribution Non-Commercial Licence 4.0. |
spellingShingle | Original Articles Moran Losada, Patricia Chouvarine, Philippe Dorda, Marie Hedtfeld, Silke Mielke, Samira Schulz, Angela Wiehlmann, Lutz Tümmler, Burkhard The cystic fibrosis lower airways microbial metagenome |
title | The cystic fibrosis lower airways microbial metagenome |
title_full | The cystic fibrosis lower airways microbial metagenome |
title_fullStr | The cystic fibrosis lower airways microbial metagenome |
title_full_unstemmed | The cystic fibrosis lower airways microbial metagenome |
title_short | The cystic fibrosis lower airways microbial metagenome |
title_sort | cystic fibrosis lower airways microbial metagenome |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5005179/ https://www.ncbi.nlm.nih.gov/pubmed/27730195 http://dx.doi.org/10.1183/23120541.00096-2015 |
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