[Integron diversity in blavim-2-carrying carbapenem-resistant clinical Pseudomonas aeruginosa isolates.]

T A Savinova1, Yu A Bocharova1, A V Lazareva1

  • 1National Medical Research Center for Children's Health Federal state autonomous institution of the Russian Federation Ministry of Health, Russia, 119296, Moscow, Russia.

Insights

Metallo-β-lactamase (MBL)-producing Pseudomonas aeruginosa are spreading in hospitals. This study characterized the VIM-2 gene in carbapenem-resistant P. aeruginosa, finding specific integron types linked to epidemic strains, aiding epidemiological tracking.

Area of Science:

  • Microbiology
  • Genetics
  • Epidemiology

Background:

  • Metallo-β-lactamase (MBL)-producing Pseudomonas aeruginosa are a growing concern in nosocomial infections.
  • Their spread is linked to clonal dissemination and horizontal gene transfer of resistance determinants via mobile genetic elements like integrons.
  • Understanding the genetic context of MBL genes is crucial for controlling their spread.

Purpose of the Study:

  • To characterize the genetic background of the VIM-2 beta-lactamase gene in carbapenem-resistant (Carba-R) P. aeruginosa clinical isolates.
  • To identify and type the integrons carrying the blaVIM-2 gene cassette.
  • To correlate integron types with specific P. aeruginosa sequence types (STs).

Main Methods:

  • Polymerase chain reaction (PCR) was used to detect class 1 integrons.
  • PCR-restriction fragment length polymorphism (RFLP) and sequencing were employed to type integrons carrying the blaVIM gene cassette.
  • Variable regions of class 1 integrons were sequenced.

Main Results:

  • Five types of blaVIM-2-carrying integrons were identified.
  • Specific integron types were associated with distinct P. aeruginosa sequence types: In56 with ST654 (over 50% of isolates), In559 with ST235 (26%), and In59-like with ST111 (19%).
  • All identified integrons, except In56, also carried genes conferring resistance to trimethoprim and/or aminoglycosides.

Conclusions:

  • The study identified a correlation between specific integron types and epidemic P. aeruginosa STs (ST111, ST654, ST235).
  • This indicates clonal dissemination of key resistance determinants.
  • The characterized integron variable regions can serve as valuable tools for the epidemiological surveillance of clinical P. aeruginosa isolates.

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