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Global genomic diversity of Pseudomonas aeruginosa in bronchiectasis.

Authors :
Harrington NE
Kottara A
Cagney K
Shepherd MJ
Grimsey EM
Fu T
Hull RC
Chong CE
Baker KS
Childs DZ
Fothergill JL
Chalmers JD
Brockhurst MA
Paterson S
Source :
The Journal of infection [J Infect] 2024 Nov; Vol. 89 (5), pp. 106275. Date of Electronic Publication: 2024 Sep 16.
Publication Year :
2024

Abstract

Objectives: Pseudomonas aeruginosa is the most common pathogen in the bronchiectasis lung, associated with worsened outcomes. P. aeruginosa genomic studies in this context have been limited to single-country, European studies. We aimed to determine strain diversity, adaptation mechanisms, and AMR features to better inform treatment.<br />Methods: P. aeruginosa from 180 bronchiectasis patients in 15 countries, obtained prior to a phase 3, randomised clinical trial (ORBIT-3), were analysed by whole-genome sequencing. Phylogenetic groups and sequence types were determined, and between versus within patient genetic diversity compared using Analysis of Molecular Variance (AMOVA). The frequency of AMR-associated genes and mutations was also determined.<br />Results: A total of 2854 P. aeruginosa isolates were analysed, predominantly belonging to phylogenetic group 1 (83%, n = 2359). Genetic diversity was far greater between than within patients, responsible for >99.9% of total diversity (AMOVA: phylogroup 1: df = 145, P < 0.01). Numerous pathways were under selection, some shared with CF (e.g., motility, iron acquisition), some unique to bronchiectasis (e.g., novel efflux pump PA1874). Multidrug resistance features were also frequent.<br />Conclusions: We present a 10-fold increase in the availability of genomic data for P. aeruginosa in bronchiectasis, highlighting key distinctions with cystic fibrosis and potential targets for future treatments.<br />Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.<br /> (Copyright © 2024 The Author(s). Published by Elsevier Ltd.. All rights reserved.)

Details

Language :
English
ISSN :
1532-2742
Volume :
89
Issue :
5
Database :
MEDLINE
Journal :
The Journal of infection
Publication Type :
Academic Journal
Accession number :
39293722
Full Text :
https://doi.org/10.1016/j.jinf.2024.106275