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

Author:

Moore Matthew P.12,Lamont Iain L.3ORCID,Williams David4ORCID,Paterson Steve4ORCID,Kukavica-Ibrulj Irena5,Tucker Nicholas P.6ORCID,Kenna Dervla T. D.7ORCID,Turton Jane F.7ORCID,Jeukens Julie5ORCID,Freschi Luca85,Wee Bryan A.910ORCID,Loman Nicholas J.11,Holden Stephen1213,Manzoor Susan14ORCID,Hawkey Peter1511ORCID,Southern Kevin W.16,Walshaw Martin J.17,Levesque Roger C.5ORCID,Fothergill Joanne L.2,Winstanley Craig2ORCID

Affiliation:

1. Present address: Nuffield Department of Health, University of Oxford, UK

2. Institute of Infection and Global Health, University of Liverpool, Liverpool, UK

3. Department of Biochemistry, University of Otago, Dunedin, New Zealand

4. Institute of Integrative Biology, University of Liverpool, Liverpool, UK

5. Institute for Integrative and Systems Biology, Université Laval, Quebec City, QC, Canada

6. Strathclyde Institute of Pharmacy & Biomedical Sciences. University of Strathclyde, Glasgow, UK

7. National Infection Service, Public Health England, London, UK

8. Present address: Harvard Medical School, Boston, MA, USA

9. Present address: Usher Institute, University of Edinburgh, Edinburgh, UK

10. School of Chemistry and Molecular Biosciences, The University of Queensland, Brisbane, QLD 4072, Australia

11. Institute for Microbiology & Infection, University of Birmingham, Birmingham, UK

12. Present address: MSD Research Laboratories, Two Pancras Square, London, UK

13. Nottingham University Hospitals NHS Trust, Nottingham, UK

14. University Hospitals Birmingham, Heartlands Hospital, Bordesley Green East, Birmingham, UK

15. Present address: University of Birmingham Microbiome Treatment Centre, College of Medical and Dental Sciences, University of Birmingham, Birmingham, UK

16. Alder Hey Children’s Hospital, Liverpool, UK

17. Liverpool Heart and Chest Hospital, Liverpool, UK

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.

Funder

Cystic Fibrosis Trust

Publisher

Microbiology Society

Subject

General Medicine

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