Global genomic epidemiology of blaGES-5 carbapenemase-associated integrons

William Matlock, Liam P. Shaw, Nicole Stoesser

Research output: Contribution to journalArticlepeer-review

3 Citations (SciVal)

Abstract

Antimicrobial resistance (AMR) gene cassettes comprise an AMR gene flanked by short recombination sites (attI and attC or attC and attC). Integrons are genetic elements able to capture, excise and shuffle these cassettes, providing ‘adaptation on demand’, and can be found on both chromosomes and plasmids. Understanding the patterns of integron diversity may help to under-stand the epidemiology of AMR genes. As a case study, we examined the clinical resistance gene blaGES-5, an integron-associated class A carbapenemase first reported in Greece in 2004 and since observed worldwide, which to our knowledge has not been the subject of a previous global analysis. Using a dataset comprising all de-duplicated NCBI contigs containing blaGES-5 (n=104), we developed a pangenome graph-based workflow to characterize and cluster the diversity of blaGES-5-associated integrons. We demonstrate that blaGES-5-associated integrons on plasmids are different to those on chromosomes. Chromosomal integrons were almost all identified in Pseudomonas aeruginosa ST235, with a consistent gene cassette content and order. We observed instances where insertion sequence IS110 disrupted attC sites, which might immobilize the gene cassettes and explain the conserved integron structure despite the presence of intI1 integrase promoters, which would typically facilitate capture or excision and rearrangement. The plasmid-associated integrons were more diverse in their gene cassette content and order, which could be an indication of greater integrase activity and ‘shuffling’ of integrons on plasmids.

Original languageEnglish
Article number001312
Pages (from-to)001312
Number of pages1
JournalMicrobial Genomics
Volume10
Issue number12
Early online date4 Dec 2024
DOIs
Publication statusPublished - 4 Dec 2024

Bibliographical note

Publisher Copyright:
© 2024 The Authors.

Data Availability Statement

All supporting data, code and protocols have been provided within the article or through supplementary data files. Five supplementary
figures and one supplementary table are available with the online version of this article

Acknowledgements

The authors would like to thank A. Sarah Walker, Célia Souque and Sally R. Partridge for the insightful conversations.

Keywords

  • beta-lactamase
  • GES
  • mobile genetic elements
  • Pseudomonas aeruginosa

ASJC Scopus subject areas

  • Epidemiology
  • Microbiology
  • Molecular Biology
  • Genetics

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