Literature DB >> 33720817

Transmission, adaptation and geographical spread of the Pseudomonas aeruginosa Liverpool epidemic strain.

Matthew P Moore1,2, Iain L Lamont3, David Williams4, Steve Paterson4, Irena Kukavica-Ibrulj5, Nicholas P Tucker6, Dervla T D Kenna7, Jane F Turton7, Julie Jeukens5, Luca Freschi8,5, Bryan A Wee9,10, Nicholas J Loman11, Stephen Holden12,13, Susan Manzoor14, Peter Hawkey15,11, Kevin W Southern16, Martin J Walshaw17, Roger C Levesque5, Joanne L Fothergill2, Craig Winstanley2.   

Abstract

The Liverpool epidemic strain (LES) is an important transmissible clonal lineage of Pseudomonas aeruginosa that chronically infects the lungs of people with cystic fibrosis (CF). Previous studies have focused on the genomics of the LES in a limited number of isolates, mostly from one CF centre in the UK, and from studies highlighting identification of the LES in Canada. Here we significantly extend the current LES genome database by genome sequencing 91 isolates from multiple CF centres across the UK, and we describe the comparative genomics of this large collection of LES isolates from the UK and Canada. Phylogenetic analysis revealed that the 145 LES genomes analysed formed a distinct clonal lineage when compared with the wider P. aeruginosa population. Notably, the isolates formed two clades: one associated with isolates from Canada, and the other associated with UK isolates. Further analysis of the UK LES isolates revealed clustering by clinic geography. Where isolates clustered closely together, the association was often supported by clinical data linking isolates or patients. When compared with the earliest known isolate, LESB58 (from 1988), many UK LES isolates shared common loss-of-function mutations, such as in genes gltR and fleR. Other loss-of-function mutations identified in previous studies as common adaptations during CF chronic lung infections were also identified in multiple LES isolates. Analysis of the LES accessory genome (including genomic islands and prophages) revealed variations in the carriage of large genomic regions, with some evidence for shared genomic island/prophage complement according to clinic location. Our study reveals divergence and adaptation during the spread of the LES, within the UK and between continents.

Entities:  

Keywords:  Pseudomonas aeruginosa; cystic fibrosis; genomics; prophage

Year:  2021        PMID: 33720817     DOI: 10.1099/mgen.0.000511

Source DB:  PubMed          Journal:  Microb Genom        ISSN: 2057-5858


  3 in total

1.  Genome evolution drives transcriptomic and phenotypic adaptation in Pseudomonas aeruginosa during 20 years of infection.

Authors:  Samuel J T Wardell; Jeff Gauthier; Lois W Martin; Marianne Potvin; Ben Brockway; Roger C Levesque; Iain L Lamont
Journal:  Microb Genom       Date:  2021-11

2.  Novel Bacteriophages Show Activity against Selected Australian Clinical Strains of Pseudomonas aeruginosa.

Authors:  Samuel Namonyo; Gilda Carvalho; Jianhua Guo; Karen D Weynberg
Journal:  Microorganisms       Date:  2022-01-19

3.  Competitive fitness of Pseudomonas aeruginosa isolates in human and murine precision-cut lung slices.

Authors:  Nina Cramer; Marie Luise Nawrot; Lion Wege; Marie Dorda; Charline Sommer; Olga Danov; Sabine Wronski; Armin Braun; Danny Jonigk; Sebastian Fischer; Antje Munder; Burkhard Tümmler
Journal:  Front Cell Infect Microbiol       Date:  2022-08-23       Impact factor: 6.073

  3 in total

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