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Lytic activity by temperate phages of Pseudomonas aeruginosa in long-term cystic fibrosis chronic lung infections

James, Chloe E; Davies, Emily V; Fothergill, Joanne L; Walshaw, Martin J; Beale, Colin M; Brockhurst, Michael A; Winstanley, Craig

Lytic activity by temperate phages of Pseudomonas aeruginosa in long-term cystic fibrosis chronic lung infections Thumbnail


Authors

Emily V Davies

Joanne L Fothergill

Martin J Walshaw

Colin M Beale

Michael A Brockhurst

Craig Winstanley



Abstract

Pseudomonas aeruginosa is the most common bacterial pathogen infecting the lungs of cystic fibrosis (CF) patients. The transmissible Liverpool epidemic strain (LES) harbours multiple inducible prophages (LESϕ2; LESϕ3; LESϕ4; LESϕ5; and LESϕ6), some of which are known to confer a competitive advantage in an in vivo rat model of chronic lung infection. We used quantitative PCR (Q-PCR) to measure the density and dynamics of all five LES phages in the sputa of 10 LES-infected CF patients over a period of 2 years. In all patients, the densities of free-LES phages were positively correlated with the densities of P. aeruginosa, and total free-phage densities consistently exceeded bacterial host densities 10–100-fold. Further, we observed a negative correlation between the phage-to-bacterium ratio and bacterial density, suggesting a role for lysis by temperate phages in regulation of the bacterial population densities. In 9/10 patients, LESϕ2 and LESϕ4 were the most abundant free phages, which reflects the differential in vitro induction properties of the phages. These data indicate that temperate phages of P. aeruginosa retain lytic activity after prolonged periods of chronic infection in the CF lung, and suggest that temperate phage lysis may contribute to regulation of P. aeruginosa density in vivo.

Citation

James, C. E., Davies, E. V., Fothergill, J. L., Walshaw, M. J., Beale, C. M., Brockhurst, M. A., & Winstanley, C. (2015). Lytic activity by temperate phages of Pseudomonas aeruginosa in long-term cystic fibrosis chronic lung infections. ISME Journal, 9(6), 1391-1398. https://doi.org/10.1038/ismej.2014.223

Journal Article Type Article
Acceptance Date Oct 23, 2014
Online Publication Date Dec 2, 2014
Publication Date Jun 1, 2015
Deposit Date Jan 12, 2015
Publicly Available Date Apr 5, 2016
Journal The ISME Journal
Print ISSN 1751-7362
Electronic ISSN 1751-7370
Publisher Nature Publishing Group
Peer Reviewed Peer Reviewed
Volume 9
Issue 6
Pages 1391-1398
DOI https://doi.org/10.1038/ismej.2014.223
Publisher URL http://dx.doi.org/10.1038/ismej.2014.223
Related Public URLs http://www.nature.com/ismej/index.html

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Version
This draft was accepted and published in December 2014





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