Literature DB >> 23706827

Molecular analysis of changes in Pseudomonas aeruginosa load during treatment of a pulmonary exacerbation in cystic fibrosis.

D W Reid1, R Latham, I L Lamont, M Camara, L F Roddam.   

Abstract

BACKGROUND: Intravenous antibiotics for pulmonary exacerbations (PEs) of cystic fibrosis (CF) usually target Pseudomonas aeruginosa. Insights into the CF lung microbiome have questioned this approach. We used RT-qPCR to determine whether intravenous antibiotics reduced P. aeruginosa numbers and whether this correlated with improved lung function. We also investigated antibiotic effects on other common respiratory pathogens in CF.
METHODS: Sputa were collected from patients when stable and again during a PE. Sputa were expectorated into a RNA preservation buffer for RNA extraction and preparation of cDNA. qPCR was used to enumerate viable P. aeruginosa as well as Streptococcus pneumoniae, Haemophilus influenzae, Staphylococcus aureus, Burkholderia cepacia complex and Aspergillus fumigatus.
RESULTS: Fifteen CF patients were followed through 21 PEs. A complete set of serial sputum samples was unavailable for two patients (three separate PEs). P. aeruginosa numbers did not increase immediately prior to a PE, but numbers during intravenous antibiotic treatment were reduced ≥4-log in 6/18 and ≥1-log in 4/18 PEs. In 7/18 PEs, P. aeruginosa numbers changed very little with intravenous antibiotics and one patient demonstrated a ≥2-log increase in P. aeruginosa load. H. influenzae and S. pneumoniae were detected in ten and five PEs respectively, but with antibiotic treatment these bacteria rapidly became undetectable in 6/10 and 4/5 PEs, respectively. There was a negative correlation between P. aeruginosa numbers and FEV1 during stable phase (r(s)=0.75, p<0.05), and reductions in P. aeruginosa load with intravenous antibiotic treatment correlated with improved FEV1 (r(s)=0.52, p<0.05).
CONCLUSIONS: Exacerbations are not due to increased P. aeruginosa numbers in CF adults. However, lung function improvements correlate with reduced P. aeruginosa burden suggesting that current antibiotic treatment strategies remain appropriate in most patients. Improved understanding of PE characterised by unchanged P. aeruginosa numbers and minimal lung function improvement following treatment may allow better targeted therapies.
Copyright © 2013 European Cystic Fibrosis Society. All rights reserved.

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Year:  2013        PMID: 23706827     DOI: 10.1016/j.jcf.2013.03.008

Source DB:  PubMed          Journal:  J Cyst Fibros        ISSN: 1569-1993            Impact factor:   5.482


  10 in total

Review 1.  Cystic Fibrosis Airway Microbiome: Overturning the Old, Opening the Way for the New.

Authors:  George A O'Toole
Journal:  J Bacteriol       Date:  2018-01-24       Impact factor: 3.490

2.  Pseudomonas aeruginosa in the Cystic Fibrosis Lung.

Authors:  John King; Ronan Murphy; Jane C Davies
Journal:  Adv Exp Med Biol       Date:  2022       Impact factor: 3.650

3.  Reduction in Pseudomonas aeruginosa sputum density during a cystic fibrosis pulmonary exacerbation does not predict clinical response.

Authors:  John C Lam; Ranjani Somayaji; Michael G Surette; Harvey R Rabin; Michael D Parkins
Journal:  BMC Infect Dis       Date:  2015-03-22       Impact factor: 3.090

4.  Bioorthogonal non-canonical amino acid tagging reveals translationally active subpopulations of the cystic fibrosis lung microbiota.

Authors:  Talia D Valentini; Sarah K Lucas; Kelsey A Binder; Lydia C Cameron; Jason A Motl; Jordan M Dunitz; Ryan C Hunter
Journal:  Nat Commun       Date:  2020-05-08       Impact factor: 14.919

5.  Heparin-binding protein in sputum as a marker of pulmonary inflammation, lung function, and bacterial load in children with cystic fibrosis.

Authors:  Gisela Hovold; Victoria Palmcrantz; Fredrik Kahn; Arne Egesten; Lisa I Påhlman
Journal:  BMC Pulm Med       Date:  2018-06-20       Impact factor: 3.317

6.  Acute effects of viral respiratory tract infections on sputum bacterial density during CF pulmonary exacerbations.

Authors:  Melanie Chin; Maya De Zoysa; Robert Slinger; Ena Gaudet; Katherine L Vandemheen; Francis Chan; Lucie Hyde; Thien-Fah Mah; Wendy Ferris; Ranjeeta Mallick; Shawn D Aaron
Journal:  J Cyst Fibros       Date:  2014-12-18       Impact factor: 5.482

Review 7.  Vaccination against respiratory Pseudomonas aeruginosa infection.

Authors:  Keith Grimwood; Jennelle M Kyd; Suzzanne J Owen; Helen M Massa; Allan W Cripps
Journal:  Hum Vaccin Immunother       Date:  2014-11-01       Impact factor: 3.452

8.  Cooperative pathogenicity in cystic fibrosis: Stenotrophomonas maltophilia modulates Pseudomonas aeruginosa virulence in mixed biofilm.

Authors:  Arianna Pompilio; Valentina Crocetta; Serena De Nicola; Fabio Verginelli; Ersilia Fiscarelli; Giovanni Di Bonaventura
Journal:  Front Microbiol       Date:  2015-09-16       Impact factor: 5.640

9.  Lung Microbiota Changes Associated with Chronic Pseudomonas aeruginosa Lung Infection and the Impact of Intravenous Colistimethate Sodium.

Authors:  David Collie; Laura Glendinning; John Govan; Steven Wright; Elisabeth Thornton; Peter Tennant; Catherine Doherty; Gerry McLachlan
Journal:  PLoS One       Date:  2015-11-06       Impact factor: 3.240

Review 10.  Bacterial microbiome of lungs in COPD.

Authors:  Marc A Sze; James C Hogg; Don D Sin
Journal:  Int J Chron Obstruct Pulmon Dis       Date:  2014-02-21
  10 in total

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