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Respiratory microbiota resistance and resilience to pulmonary exacerbation and subsequent antimicrobial intervention

Pulmonary symptoms in cystic fibrosis (CF) begin in early life with chronic lung infections and concomitant airway inflammation leading to progressive loss of lung function. Gradual pulmonary function decline is interspersed with periods of acute worsening of respiratory symptoms known as CF pulmona...

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Autores principales: Cuthbertson, Leah, Rogers, Geraint B, Walker, Alan W, Oliver, Anna, Green, Laura E, Daniels, Thomas W V, Carroll, Mary P, Parkhill, Julian, Bruce, Kenneth D, van der Gast, Christopher J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4820042/
https://www.ncbi.nlm.nih.gov/pubmed/26555248
http://dx.doi.org/10.1038/ismej.2015.198
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author Cuthbertson, Leah
Rogers, Geraint B
Walker, Alan W
Oliver, Anna
Green, Laura E
Daniels, Thomas W V
Carroll, Mary P
Parkhill, Julian
Bruce, Kenneth D
van der Gast, Christopher J
author_facet Cuthbertson, Leah
Rogers, Geraint B
Walker, Alan W
Oliver, Anna
Green, Laura E
Daniels, Thomas W V
Carroll, Mary P
Parkhill, Julian
Bruce, Kenneth D
van der Gast, Christopher J
author_sort Cuthbertson, Leah
collection PubMed
description Pulmonary symptoms in cystic fibrosis (CF) begin in early life with chronic lung infections and concomitant airway inflammation leading to progressive loss of lung function. Gradual pulmonary function decline is interspersed with periods of acute worsening of respiratory symptoms known as CF pulmonary exacerbations (CFPEs). Cumulatively, CFPEs are associated with more rapid disease progression. In this study multiple sputum samples were collected from adult CF patients over the course of CFPEs to better understand how changes in microbiota are associated with CFPE onset and management. Data were divided into five clinical periods: pre-CFPE baseline, CFPE, antibiotic treatment, recovery, and post-CFPE baseline. Samples were treated with propidium monoazide prior to DNA extraction, to remove the impact of bacterial cell death artefacts following antibiotic treatment, and then characterised by 16S rRNA gene-targeted high-throughput sequencing. Partitioning CF microbiota into core and rare groups revealed compositional resistance to CFPE and resilience to antibiotics interventions. Mixed effects modelling of core microbiota members revealed no significant negative impact on the relative abundance of Pseudomonas aeruginosa across the exacerbation cycle. Our findings have implications for current CFPE management strategies, supporting reassessment of existing antimicrobial treatment regimens, as antimicrobial resistance by pathogens and other members of the microbiota may be significant contributing factors.
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spelling pubmed-48200422016-09-21 Respiratory microbiota resistance and resilience to pulmonary exacerbation and subsequent antimicrobial intervention Cuthbertson, Leah Rogers, Geraint B Walker, Alan W Oliver, Anna Green, Laura E Daniels, Thomas W V Carroll, Mary P Parkhill, Julian Bruce, Kenneth D van der Gast, Christopher J ISME J Original Article Pulmonary symptoms in cystic fibrosis (CF) begin in early life with chronic lung infections and concomitant airway inflammation leading to progressive loss of lung function. Gradual pulmonary function decline is interspersed with periods of acute worsening of respiratory symptoms known as CF pulmonary exacerbations (CFPEs). Cumulatively, CFPEs are associated with more rapid disease progression. In this study multiple sputum samples were collected from adult CF patients over the course of CFPEs to better understand how changes in microbiota are associated with CFPE onset and management. Data were divided into five clinical periods: pre-CFPE baseline, CFPE, antibiotic treatment, recovery, and post-CFPE baseline. Samples were treated with propidium monoazide prior to DNA extraction, to remove the impact of bacterial cell death artefacts following antibiotic treatment, and then characterised by 16S rRNA gene-targeted high-throughput sequencing. Partitioning CF microbiota into core and rare groups revealed compositional resistance to CFPE and resilience to antibiotics interventions. Mixed effects modelling of core microbiota members revealed no significant negative impact on the relative abundance of Pseudomonas aeruginosa across the exacerbation cycle. Our findings have implications for current CFPE management strategies, supporting reassessment of existing antimicrobial treatment regimens, as antimicrobial resistance by pathogens and other members of the microbiota may be significant contributing factors. Nature Publishing Group 2016-05 2015-11-10 /pmc/articles/PMC4820042/ /pubmed/26555248 http://dx.doi.org/10.1038/ismej.2015.198 Text en Copyright © 2016 International Society for Microbial Ecology http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Original Article
Cuthbertson, Leah
Rogers, Geraint B
Walker, Alan W
Oliver, Anna
Green, Laura E
Daniels, Thomas W V
Carroll, Mary P
Parkhill, Julian
Bruce, Kenneth D
van der Gast, Christopher J
Respiratory microbiota resistance and resilience to pulmonary exacerbation and subsequent antimicrobial intervention
title Respiratory microbiota resistance and resilience to pulmonary exacerbation and subsequent antimicrobial intervention
title_full Respiratory microbiota resistance and resilience to pulmonary exacerbation and subsequent antimicrobial intervention
title_fullStr Respiratory microbiota resistance and resilience to pulmonary exacerbation and subsequent antimicrobial intervention
title_full_unstemmed Respiratory microbiota resistance and resilience to pulmonary exacerbation and subsequent antimicrobial intervention
title_short Respiratory microbiota resistance and resilience to pulmonary exacerbation and subsequent antimicrobial intervention
title_sort respiratory microbiota resistance and resilience to pulmonary exacerbation and subsequent antimicrobial intervention
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4820042/
https://www.ncbi.nlm.nih.gov/pubmed/26555248
http://dx.doi.org/10.1038/ismej.2015.198
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