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Evolutionary diversification of Pseudomonas aeruginosa in an artificial sputum model

BACKGROUND: During chronic lung infections of cystic fibrosis patients Pseudomonas aeruginosa populations undergo extensive evolutionary diversification. However, the selective drivers of this evolutionary process are poorly understood. To test the effects of temperate phages on diversification in P...

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Autores principales: Davies, Emily V., James, Chloe E., Brockhurst, Michael A., Winstanley, Craig
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5216580/
https://www.ncbi.nlm.nih.gov/pubmed/28056789
http://dx.doi.org/10.1186/s12866-016-0916-z
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author Davies, Emily V.
James, Chloe E.
Brockhurst, Michael A.
Winstanley, Craig
author_facet Davies, Emily V.
James, Chloe E.
Brockhurst, Michael A.
Winstanley, Craig
author_sort Davies, Emily V.
collection PubMed
description BACKGROUND: During chronic lung infections of cystic fibrosis patients Pseudomonas aeruginosa populations undergo extensive evolutionary diversification. However, the selective drivers of this evolutionary process are poorly understood. To test the effects of temperate phages on diversification in P. aeruginosa biofilms we experimentally evolved populations of P. aeruginosa for approximately 240 generations in artificial sputum medium with or without a community of three temperate phages. RESULTS: Analysis of end-point populations using a suite of phenotypic tests revealed extensive phenotypic diversification within populations, but no significant differences between the populations evolved with or without phages. The most common phenotypic variant observed was loss of all three types of motility (swimming, swarming and twitching) and resistance to all three phages. Despite the absence of selective pressure, some members of the population evolved antibiotic resistance. The frequency of antibiotic resistant isolates varied according to population and the antibiotic tested. However, resistance to ceftazidime and tazobactam-piperacillin was observed more frequently than resistance to other antibiotics, and was associated with higher prevelence of isolates exhibiting a hypermutable phenotype and increased beta-lactamase production. CONCLUSIONS: We observed considerable within-population phenotypic diversity in P. aeruginosa populations evolving in the artificial sputum medium biofilm model. Replicate populations evolved both in the presence and absence of phages converged upon similar sets of phenotypes. The evolved phenotypes, including antimicrobial resistance, were similar to those observed amongst clinical isolates from cystic fibrosis infections. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12866-016-0916-z) contains supplementary material, which is available to authorized users.
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spelling pubmed-52165802017-01-09 Evolutionary diversification of Pseudomonas aeruginosa in an artificial sputum model Davies, Emily V. James, Chloe E. Brockhurst, Michael A. Winstanley, Craig BMC Microbiol Research Article BACKGROUND: During chronic lung infections of cystic fibrosis patients Pseudomonas aeruginosa populations undergo extensive evolutionary diversification. However, the selective drivers of this evolutionary process are poorly understood. To test the effects of temperate phages on diversification in P. aeruginosa biofilms we experimentally evolved populations of P. aeruginosa for approximately 240 generations in artificial sputum medium with or without a community of three temperate phages. RESULTS: Analysis of end-point populations using a suite of phenotypic tests revealed extensive phenotypic diversification within populations, but no significant differences between the populations evolved with or without phages. The most common phenotypic variant observed was loss of all three types of motility (swimming, swarming and twitching) and resistance to all three phages. Despite the absence of selective pressure, some members of the population evolved antibiotic resistance. The frequency of antibiotic resistant isolates varied according to population and the antibiotic tested. However, resistance to ceftazidime and tazobactam-piperacillin was observed more frequently than resistance to other antibiotics, and was associated with higher prevelence of isolates exhibiting a hypermutable phenotype and increased beta-lactamase production. CONCLUSIONS: We observed considerable within-population phenotypic diversity in P. aeruginosa populations evolving in the artificial sputum medium biofilm model. Replicate populations evolved both in the presence and absence of phages converged upon similar sets of phenotypes. The evolved phenotypes, including antimicrobial resistance, were similar to those observed amongst clinical isolates from cystic fibrosis infections. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12866-016-0916-z) contains supplementary material, which is available to authorized users. BioMed Central 2017-01-05 /pmc/articles/PMC5216580/ /pubmed/28056789 http://dx.doi.org/10.1186/s12866-016-0916-z Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Davies, Emily V.
James, Chloe E.
Brockhurst, Michael A.
Winstanley, Craig
Evolutionary diversification of Pseudomonas aeruginosa in an artificial sputum model
title Evolutionary diversification of Pseudomonas aeruginosa in an artificial sputum model
title_full Evolutionary diversification of Pseudomonas aeruginosa in an artificial sputum model
title_fullStr Evolutionary diversification of Pseudomonas aeruginosa in an artificial sputum model
title_full_unstemmed Evolutionary diversification of Pseudomonas aeruginosa in an artificial sputum model
title_short Evolutionary diversification of Pseudomonas aeruginosa in an artificial sputum model
title_sort evolutionary diversification of pseudomonas aeruginosa in an artificial sputum model
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5216580/
https://www.ncbi.nlm.nih.gov/pubmed/28056789
http://dx.doi.org/10.1186/s12866-016-0916-z
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