Cargando…
Microbiota and Metabolite Profiling Reveal Specific Alterations in Bacterial Community Structure and Environment in the Cystic Fibrosis Airway during Exacerbation
Chronic polymicrobial infections of the lung are the foremost cause of morbidity and mortality in cystic fibrosis (CF) patients. The composition of the microbial flora of the airway alters considerably during infection, particularly during patient exacerbation. An understanding of which organisms ar...
Autores principales: | , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3866110/ https://www.ncbi.nlm.nih.gov/pubmed/24358183 http://dx.doi.org/10.1371/journal.pone.0082432 |
_version_ | 1782296110856929280 |
---|---|
author | Twomey, Kate B. Alston, Mark An, Shi-Qi O'Connell, Oisin J. McCarthy, Yvonne Swarbreck, David Febrer, Melanie Dow, J. Maxwell Plant, Barry J. Ryan, Robert P. |
author_facet | Twomey, Kate B. Alston, Mark An, Shi-Qi O'Connell, Oisin J. McCarthy, Yvonne Swarbreck, David Febrer, Melanie Dow, J. Maxwell Plant, Barry J. Ryan, Robert P. |
author_sort | Twomey, Kate B. |
collection | PubMed |
description | Chronic polymicrobial infections of the lung are the foremost cause of morbidity and mortality in cystic fibrosis (CF) patients. The composition of the microbial flora of the airway alters considerably during infection, particularly during patient exacerbation. An understanding of which organisms are growing, their environment and their behaviour in the airway is of importance for designing antibiotic treatment regimes and for patient prognosis. To this end, we have analysed sputum samples taken from separate cohorts of CF and non-CF subjects for metabolites and in parallel, and we have examined both isolated DNA and RNA for the presence of 16S rRNA genes and transcripts by high-throughput sequencing of amplicon or cDNA libraries. This analysis revealed that although the population size of all dominant orders of bacteria as measured by DNA- and RNA- based methods are similar, greater discrepancies are seen with less prevalent organisms, some of which we associated with CF for the first time. Additionally, we identified a strong relationship between the abundance of specific anaerobes and fluctuations in several metabolites including lactate and putrescine during patient exacerbation. This study has hence identified organisms whose occurrence within the CF microbiome has been hitherto unreported and has revealed potential metabolic biomarkers for exacerbation. |
format | Online Article Text |
id | pubmed-3866110 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-38661102013-12-19 Microbiota and Metabolite Profiling Reveal Specific Alterations in Bacterial Community Structure and Environment in the Cystic Fibrosis Airway during Exacerbation Twomey, Kate B. Alston, Mark An, Shi-Qi O'Connell, Oisin J. McCarthy, Yvonne Swarbreck, David Febrer, Melanie Dow, J. Maxwell Plant, Barry J. Ryan, Robert P. PLoS One Research Article Chronic polymicrobial infections of the lung are the foremost cause of morbidity and mortality in cystic fibrosis (CF) patients. The composition of the microbial flora of the airway alters considerably during infection, particularly during patient exacerbation. An understanding of which organisms are growing, their environment and their behaviour in the airway is of importance for designing antibiotic treatment regimes and for patient prognosis. To this end, we have analysed sputum samples taken from separate cohorts of CF and non-CF subjects for metabolites and in parallel, and we have examined both isolated DNA and RNA for the presence of 16S rRNA genes and transcripts by high-throughput sequencing of amplicon or cDNA libraries. This analysis revealed that although the population size of all dominant orders of bacteria as measured by DNA- and RNA- based methods are similar, greater discrepancies are seen with less prevalent organisms, some of which we associated with CF for the first time. Additionally, we identified a strong relationship between the abundance of specific anaerobes and fluctuations in several metabolites including lactate and putrescine during patient exacerbation. This study has hence identified organisms whose occurrence within the CF microbiome has been hitherto unreported and has revealed potential metabolic biomarkers for exacerbation. Public Library of Science 2013-12-17 /pmc/articles/PMC3866110/ /pubmed/24358183 http://dx.doi.org/10.1371/journal.pone.0082432 Text en © 2013 Twomey 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, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Twomey, Kate B. Alston, Mark An, Shi-Qi O'Connell, Oisin J. McCarthy, Yvonne Swarbreck, David Febrer, Melanie Dow, J. Maxwell Plant, Barry J. Ryan, Robert P. Microbiota and Metabolite Profiling Reveal Specific Alterations in Bacterial Community Structure and Environment in the Cystic Fibrosis Airway during Exacerbation |
title | Microbiota and Metabolite Profiling Reveal Specific Alterations in Bacterial Community Structure and Environment in the Cystic Fibrosis Airway during Exacerbation |
title_full | Microbiota and Metabolite Profiling Reveal Specific Alterations in Bacterial Community Structure and Environment in the Cystic Fibrosis Airway during Exacerbation |
title_fullStr | Microbiota and Metabolite Profiling Reveal Specific Alterations in Bacterial Community Structure and Environment in the Cystic Fibrosis Airway during Exacerbation |
title_full_unstemmed | Microbiota and Metabolite Profiling Reveal Specific Alterations in Bacterial Community Structure and Environment in the Cystic Fibrosis Airway during Exacerbation |
title_short | Microbiota and Metabolite Profiling Reveal Specific Alterations in Bacterial Community Structure and Environment in the Cystic Fibrosis Airway during Exacerbation |
title_sort | microbiota and metabolite profiling reveal specific alterations in bacterial community structure and environment in the cystic fibrosis airway during exacerbation |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3866110/ https://www.ncbi.nlm.nih.gov/pubmed/24358183 http://dx.doi.org/10.1371/journal.pone.0082432 |
work_keys_str_mv | AT twomeykateb microbiotaandmetaboliteprofilingrevealspecificalterationsinbacterialcommunitystructureandenvironmentinthecysticfibrosisairwayduringexacerbation AT alstonmark microbiotaandmetaboliteprofilingrevealspecificalterationsinbacterialcommunitystructureandenvironmentinthecysticfibrosisairwayduringexacerbation AT anshiqi microbiotaandmetaboliteprofilingrevealspecificalterationsinbacterialcommunitystructureandenvironmentinthecysticfibrosisairwayduringexacerbation AT oconnelloisinj microbiotaandmetaboliteprofilingrevealspecificalterationsinbacterialcommunitystructureandenvironmentinthecysticfibrosisairwayduringexacerbation AT mccarthyyvonne microbiotaandmetaboliteprofilingrevealspecificalterationsinbacterialcommunitystructureandenvironmentinthecysticfibrosisairwayduringexacerbation AT swarbreckdavid microbiotaandmetaboliteprofilingrevealspecificalterationsinbacterialcommunitystructureandenvironmentinthecysticfibrosisairwayduringexacerbation AT febrermelanie microbiotaandmetaboliteprofilingrevealspecificalterationsinbacterialcommunitystructureandenvironmentinthecysticfibrosisairwayduringexacerbation AT dowjmaxwell microbiotaandmetaboliteprofilingrevealspecificalterationsinbacterialcommunitystructureandenvironmentinthecysticfibrosisairwayduringexacerbation AT plantbarryj microbiotaandmetaboliteprofilingrevealspecificalterationsinbacterialcommunitystructureandenvironmentinthecysticfibrosisairwayduringexacerbation AT ryanrobertp microbiotaandmetaboliteprofilingrevealspecificalterationsinbacterialcommunitystructureandenvironmentinthecysticfibrosisairwayduringexacerbation |