Characterisation of a class 1 integron associated with the formation of quadruple blaGES-5 cassettes from an IncP-1β group plasmid in Pseudomonas aeruginosa

Int J Antimicrob Agents. 2018 Oct;52(4):485-491. doi: 10.1016/j.ijantimicag.2018.07.002. Epub 2018 Jul 31.

Abstract

Integrons are genetic platforms responsible for the dissemination of antimicrobial resistance genes among Gram-negative bacteria, primarily due to their association with transposable elements and conjugative plasmids. In this study, a cassette array containing four identical blaGES-5 genes embedded in a class 1 integron located on an IncP-1β group plasmid from a clinical Pseudomonas aeruginosa strain was identified. Comparative genome analysis and conjugation assay showed that the plasmid pICP-4GES lacked the trbN, trbO and trbP genes but was conjugable. Antimicrobial susceptibility testing revealed that compared with single-copy blaGES-5 complementary strains, both the cloned and chromosome-targeted expression of four copies of blaGES-5 increased the minimum inhibitory concentration (MIC) by one to two dilutions for most of the selected antimicrobials. Quantitative real-time reverse transcription PCR (RT-qPCR) showed that the four consecutive cassettes increased blaGES-5 expression by approximately two-fold compared with the single-copy blaGES-5 strain, suggesting that the level of gene expression was not directly proportional to copy number. In addition, the gene cassette capture assay showed that the global blaGES-5 transfer frequency reached 5.38 × 10-4.

Keywords: Carbapenem resistance; Class 1 integron; Gene cassette; IncP-1β group plasmid; Pseudomonas aeruginosa.

MeSH terms

  • Anti-Bacterial Agents / pharmacology
  • Base Sequence
  • Conjugation, Genetic
  • DNA Transposable Elements
  • Gene Expression Regulation, Bacterial*
  • Genome, Bacterial*
  • Humans
  • Integrons*
  • Microbial Sensitivity Tests
  • Multigene Family
  • Plasmids / chemistry
  • Plasmids / metabolism
  • Pseudomonas Infections / microbiology
  • Pseudomonas aeruginosa / drug effects
  • Pseudomonas aeruginosa / enzymology
  • Pseudomonas aeruginosa / genetics*
  • Pseudomonas aeruginosa / isolation & purification
  • beta-Lactamases / genetics*
  • beta-Lactamases / metabolism

Substances

  • Anti-Bacterial Agents
  • DNA Transposable Elements
  • beta-Lactamases