Abstract
AbstractAntimicrobial resistance (AMR) gene cassettes comprise an AMR gene flanked by short recombination sites (attI×attCorattC×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 understand the epidemiology of AMR genes. As a case study, we examined the clinical resistance geneblaGES-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 NCBI contigs containingblaGES-5(n= 431), we developed a pangenome graph-based workflow to characterise and cluster the diversity ofblaGES-5-associated integrons. We demonstrate thatblaGES-5-associated integrons on plasmids are different to those on chromosomes. Chromosomal integrons were almost all identified inP. aeruginosaST235, with a consistent gene cassette content and order. We observed instances where insertion sequence IS110disruptedattCsites, which might immobilise the gene cassettes and explain the conserved integron structure despite the presence ofintI1integrase 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.
Publisher
Cold Spring Harbor Laboratory