Pyrosequencing reveals transient cystic fibrosis lung microbiome changes with intravenous antibiotics

Chronic airway infection in adults with cystic fibrosis (CF) is polymicrobial and the impact of intravenous antibiotics on the bacterial community composition is poorly understood. We employed culture-independent molecular techniques to explore the early effects of i.v. antibiotics on the CF airway...

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Published inThe European respiratory journal Vol. 44; no. 4; pp. 922 - 930
Main Authors Smith, Daniel J., Badrick, Alison C., Zakrzewski, Martha, Krause, Lutz, Bell, Scott C., Anderson, Gregory J., Reid, David W.
Format Journal Article
LanguageEnglish
Published Leeds Maney 01.10.2014
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Abstract Chronic airway infection in adults with cystic fibrosis (CF) is polymicrobial and the impact of intravenous antibiotics on the bacterial community composition is poorly understood. We employed culture-independent molecular techniques to explore the early effects of i.v. antibiotics on the CF airway microbiome. DNA was extracted from sputum samples collected from adult subjects with CF at three time-points (before starting treatment, and at day 3 and day 8–10 of i.v. antibiotics) during treatment of an infective pulmonary exacerbation. Microbial community profiles were derived through analysis of bacterial-derived 16S ribosomal RNA by pyrosequencing and changes over time were compared. 59 sputum samples were collected during 24 pulmonary exacerbations from 23 subjects. Between treatment onset and day 3 there was a significant reduction in the relative abundance of Pseudomonas and increased microbial diversity. By day 8–10, bacterial community composition was similar to pre-treatment. Changes in community composition did not predict improvements in lung function. The relative abundance of Pseudomonas falls rapidly in subjects with CF receiving i.v. antibiotic treatment for a pulmonary exacerbation and is accompanied by an increase in overall microbial diversity. However, this effect is not maintained beyond the first week of treatment.
AbstractList Chronic airway infection in adults with cystic fibrosis (CF) is polymicrobial and the impact of intravenous antibiotics on the bacterial community composition is poorly understood. We employed culture-independent molecular techniques to explore the early effects of i.v. antibiotics on the CF airway microbiome. DNA was extracted from sputum samples collected from adult subjects with CF at three time-points (before starting treatment, and at day 3 and day 8-10 of i.v. antibiotics) during treatment of an infective pulmonary exacerbation. Microbial community profiles were derived through analysis of bacterial-derived 16S ribosomal RNA by pyrosequencing and changes over time were compared. 59 sputum samples were collected during 24 pulmonary exacerbations from 23 subjects. Between treatment onset and day 3 there was a significant reduction in the relative abundance of Pseudomonas and increased microbial diversity. By day 8-10, bacterial community composition was similar to pre-treatment. Changes in community composition did not predict improvements in lung function. The relative abundance of Pseudomonas falls rapidly in subjects with CF receiving i.v. antibiotic treatment for a pulmonary exacerbation and is accompanied by an increase in overall microbial diversity. However, this effect is not maintained beyond the first week of treatment.
Chronic airway infection in adults with cystic fibrosis (CF) is polymicrobial and the impact of intravenous antibiotics on the bacterial community composition is poorly understood. We employed culture-independent molecular techniques to explore the early effects of i.v. antibiotics on the CF airway microbiome. DNA was extracted from sputum samples collected from adult subjects with CF at three time-points (before starting treatment, and at day 3 and day 8–10 of i.v. antibiotics) during treatment of an infective pulmonary exacerbation. Microbial community profiles were derived through analysis of bacterial-derived 16S ribosomal RNA by pyrosequencing and changes over time were compared. 59 sputum samples were collected during 24 pulmonary exacerbations from 23 subjects. Between treatment onset and day 3 there was a significant reduction in the relative abundance of Pseudomonas and increased microbial diversity. By day 8–10, bacterial community composition was similar to pre-treatment. Changes in community composition did not predict improvements in lung function. The relative abundance of Pseudomonas falls rapidly in subjects with CF receiving i.v. antibiotic treatment for a pulmonary exacerbation and is accompanied by an increase in overall microbial diversity. However, this effect is not maintained beyond the first week of treatment.
Chronic airway infection in adults with cystic fibrosis (CF) is polymicrobial and the impact of intravenous antibiotics on the bacterial community composition is poorly understood. We employed culture-independent molecular techniques to explore the early effects of i.v. antibiotics on the CF airway microbiome. DNA was extracted from sputum samples collected from adult subjects with CF at three time-points (before starting treatment, and at day 3 and day 8-10 of i.v. antibiotics) during treatment of an infective pulmonary exacerbation. Microbial community profiles were derived through analysis of bacterial-derived 16S ribosomal RNA by pyrosequencing and changes over time were compared. 59 sputum samples were collected during 24 pulmonary exacerbations from 23 subjects. Between treatment onset and day 3 there was a significant reduction in the relative abundance of Pseudomonas and increased microbial diversity. By day 8-10, bacterial community composition was similar to pre-treatment. Changes in community composition did not predict improvements in lung function. The relative abundance of Pseudomonas falls rapidly in subjects with CF receiving i.v. antibiotic treatment for a pulmonary exacerbation and is accompanied by an increase in overall microbial diversity. However, this effect is not maintained beyond the first week of treatment.Chronic airway infection in adults with cystic fibrosis (CF) is polymicrobial and the impact of intravenous antibiotics on the bacterial community composition is poorly understood. We employed culture-independent molecular techniques to explore the early effects of i.v. antibiotics on the CF airway microbiome. DNA was extracted from sputum samples collected from adult subjects with CF at three time-points (before starting treatment, and at day 3 and day 8-10 of i.v. antibiotics) during treatment of an infective pulmonary exacerbation. Microbial community profiles were derived through analysis of bacterial-derived 16S ribosomal RNA by pyrosequencing and changes over time were compared. 59 sputum samples were collected during 24 pulmonary exacerbations from 23 subjects. Between treatment onset and day 3 there was a significant reduction in the relative abundance of Pseudomonas and increased microbial diversity. By day 8-10, bacterial community composition was similar to pre-treatment. Changes in community composition did not predict improvements in lung function. The relative abundance of Pseudomonas falls rapidly in subjects with CF receiving i.v. antibiotic treatment for a pulmonary exacerbation and is accompanied by an increase in overall microbial diversity. However, this effect is not maintained beyond the first week of treatment.
Author Bell, Scott C.
Krause, Lutz
Badrick, Alison C.
Reid, David W.
Smith, Daniel J.
Zakrzewski, Martha
Anderson, Gregory J.
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Cites_doi 10.1136/thoraxjnl-2011-201498
10.1371/journal.pone.0016384
10.1038/ismej.2011.82
10.1128/JCM.42.11.5176-5183.2004
10.1164/rccm.200812-1845PP
10.1016/j.jcf.2011.05.002
10.1016/j.tim.2011.04.005
10.1111/j.1469-0691.2010.03189.x
10.1371/journal.pone.0022702
10.1016/j.jcf.2012.10.004
10.1371/journal.pone.0011044
10.1046/j.1365-2362.2000.00667.x
10.2217/fmb.12.55
10.1099/mic.0.2006/004077-0
10.1038/ismej.2012.145
10.1016/j.jcf.2013.03.008
10.1099/jmm.0.015875-0
10.1093/bioinformatics/btq461
10.1016/j.jcf.2012.05.008
10.1016/j.diagmicrobio.2008.06.011
10.1038/nmeth.f.303
10.1016/j.prrv.2010.07.003
10.1136/thx.2010.137281
10.1164/rccm.201009-1478CI
10.1089/fpd.2008.0107
10.1128/CMR.00068-09
10.1128/JB.00566-12
10.1186/1471-2105-12-385
10.1128/AEM.03006-05
10.1073/pnas.1120577109
10.1183/09031936.00166412
10.1101/gr.112730.110
10.1186/1471-2466-9-14
10.1164/rccm.201001-0057OC
10.1164/rccm.200708-1151OC
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Keywords Antibiotic
Intravenous administration
Respiratory disease
Lung
Metabolic diseases
Digestive diseases
Cystic fibrosis
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References 2024102022572023000_44.4.922.1
2024102022572023000_44.4.922.2
2024102022572023000_44.4.922.3
2024102022572023000_44.4.922.19
2024102022572023000_44.4.922.4
2024102022572023000_44.4.922.5
Flume (2024102022572023000_44.4.922.30) 2009; 54
2024102022572023000_44.4.922.6
2024102022572023000_44.4.922.7
2024102022572023000_44.4.922.8
2024102022572023000_44.4.922.14
2024102022572023000_44.4.922.36
2024102022572023000_44.4.922.9
2024102022572023000_44.4.922.35
2024102022572023000_44.4.922.12
2024102022572023000_44.4.922.34
2024102022572023000_44.4.922.11
2024102022572023000_44.4.922.33
2024102022572023000_44.4.922.18
2024102022572023000_44.4.922.17
2024102022572023000_44.4.922.16
2024102022572023000_44.4.922.38
2024102022572023000_44.4.922.15
2024102022572023000_44.4.922.37
2024102022572023000_44.4.922.10
2024102022572023000_44.4.922.32
2024102022572023000_44.4.922.31
2024102022572023000_44.4.922.25
2024102022572023000_44.4.922.24
2024102022572023000_44.4.922.23
2024102022572023000_44.4.922.22
2024102022572023000_44.4.922.29
Plummer (2024102022572023000_44.4.922.13) 2011; 1
2024102022572023000_44.4.922.28
2024102022572023000_44.4.922.27
2024102022572023000_44.4.922.26
2024102022572023000_44.4.922.21
2024102022572023000_44.4.922.20
References_xml – ident: 2024102022572023000_44.4.922.2
  doi: 10.1136/thoraxjnl-2011-201498
– ident: 2024102022572023000_44.4.922.37
  doi: 10.1371/journal.pone.0016384
– ident: 2024102022572023000_44.4.922.38
  doi: 10.1038/ismej.2011.82
– ident: 2024102022572023000_44.4.922.7
  doi: 10.1128/JCM.42.11.5176-5183.2004
– ident: 2024102022572023000_44.4.922.29
  doi: 10.1164/rccm.200812-1845PP
– ident: 2024102022572023000_44.4.922.1
– ident: 2024102022572023000_44.4.922.26
  doi: 10.1016/j.jcf.2011.05.002
– ident: 2024102022572023000_44.4.922.27
  doi: 10.1016/j.tim.2011.04.005
– ident: 2024102022572023000_44.4.922.35
  doi: 10.1111/j.1469-0691.2010.03189.x
– ident: 2024102022572023000_44.4.922.6
  doi: 10.1371/journal.pone.0022702
– ident: 2024102022572023000_44.4.922.12
  doi: 10.1016/j.jcf.2012.10.004
– ident: 2024102022572023000_44.4.922.33
  doi: 10.1371/journal.pone.0011044
– ident: 2024102022572023000_44.4.922.14
  doi: 10.1046/j.1365-2362.2000.00667.x
– ident: 2024102022572023000_44.4.922.8
  doi: 10.2217/fmb.12.55
– ident: 2024102022572023000_44.4.922.5
  doi: 10.1099/mic.0.2006/004077-0
– ident: 2024102022572023000_44.4.922.21
  doi: 10.1038/ismej.2012.145
– ident: 2024102022572023000_44.4.922.23
  doi: 10.1016/j.jcf.2013.03.008
– ident: 2024102022572023000_44.4.922.28
  doi: 10.1099/jmm.0.015875-0
– ident: 2024102022572023000_44.4.922.19
  doi: 10.1093/bioinformatics/btq461
– ident: 2024102022572023000_44.4.922.24
  doi: 10.1016/j.jcf.2012.05.008
– ident: 2024102022572023000_44.4.922.34
  doi: 10.1016/j.diagmicrobio.2008.06.011
– ident: 2024102022572023000_44.4.922.17
  doi: 10.1038/nmeth.f.303
– ident: 2024102022572023000_44.4.922.4
  doi: 10.1016/j.prrv.2010.07.003
– ident: 2024102022572023000_44.4.922.9
  doi: 10.1136/thx.2010.137281
– ident: 2024102022572023000_44.4.922.10
  doi: 10.1164/rccm.201009-1478CI
– ident: 2024102022572023000_44.4.922.16
  doi: 10.1089/fpd.2008.0107
– ident: 2024102022572023000_44.4.922.31
  doi: 10.1128/CMR.00068-09
– ident: 2024102022572023000_44.4.922.32
  doi: 10.1128/JB.00566-12
– ident: 2024102022572023000_44.4.922.22
  doi: 10.1186/1471-2105-12-385
– volume: 54
  start-page: 522
  year: 2009
  ident: 2024102022572023000_44.4.922.30
  article-title: Cystic fibrosis pulmonary guidelines: airway clearance therapies
  publication-title: Respir Care
– ident: 2024102022572023000_44.4.922.20
  doi: 10.1128/AEM.03006-05
– ident: 2024102022572023000_44.4.922.25
  doi: 10.1073/pnas.1120577109
– volume: 1
  start-page: CD006682
  year: 2011
  ident: 2024102022572023000_44.4.922.13
  article-title: Duration of intravenous antibiotic therapy in people with cystic fibrosis
  publication-title: Cochrane Database Syst Rev
– ident: 2024102022572023000_44.4.922.11
  doi: 10.1183/09031936.00166412
– ident: 2024102022572023000_44.4.922.18
  doi: 10.1101/gr.112730.110
– ident: 2024102022572023000_44.4.922.3
  doi: 10.1186/1471-2466-9-14
– ident: 2024102022572023000_44.4.922.15
  doi: 10.1164/rccm.201001-0057OC
– ident: 2024102022572023000_44.4.922.36
  doi: 10.1164/rccm.200708-1151OC
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Snippet Chronic airway infection in adults with cystic fibrosis (CF) is polymicrobial and the impact of intravenous antibiotics on the bacterial community composition...
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SubjectTerms Adolescent
Adult
Anti-Bacterial Agents - administration & dosage
Biological and medical sciences
Cystic Fibrosis - drug therapy
Cystic Fibrosis - microbiology
Diphosphates
DNA, Bacterial - analysis
Errors of metabolism
Female
Humans
Injections, Intravenous
Lung - microbiology
Male
Medical sciences
Metabolic diseases
Microbiota
Middle Aged
Miscellaneous hereditary metabolic disorders
Pneumology
Pseudomonas
Sequence Analysis, DNA - methods
Young Adult
Title Pyrosequencing reveals transient cystic fibrosis lung microbiome changes with intravenous antibiotics
URI https://www.ncbi.nlm.nih.gov/pubmed/25034564
https://www.proquest.com/docview/1567050666
https://www.proquest.com/docview/1808626040
Volume 44
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