Detection of vim- and ipm-type metallo-beta-lactamases in Pseudomonas aeruginosa clinical isolates

Saeed Sepehriseresht1, Mohammad Ali Boroumand, Leila Pourgholi

  • 1Molecular Pathology Department, Tehran Heart Center, Tehran University of Medical Sciences, Tehran, Iran.

Abstract

Insights

Metallo-beta-lactamase (MBL) genes, including newer variants, are increasingly detected in Pseudomonas aeruginosa from burn wounds, contributing to rising imipenem resistance. This necessitates urgent strategies to combat MBL production in clinical settings.

Area of Science:

  • Medical Microbiology
  • Infectious Diseases
  • Antimicrobial Resistance

Background:

  • Pseudomonas aeruginosa is a primary cause of burn wound infections.
  • Increasing metallo-beta-lactamase (MBL) mediated resistance to imipenem poses a significant treatment challenge.
  • This study focuses on Iranian burn wound isolates.

Purpose of the Study:

  • To detect specific MBL genes (vim1, vim2, ipm1, ipm2) in Pseudomonas aeruginosa.
  • To investigate the prevalence of these genes in imipenem-resistant and intermediate isolates.
  • To assess the contribution of MBLs to imipenem resistance in burn wound infections.

Main Methods:

  • Isolation and biochemical confirmation of 483 P. aeruginosa strains from burn infections.
  • Determination of imipenem susceptibility using the Kirby-Bauer method.
  • Screening for MBL genes (vim1, vim2, ipm1, ipm2) via Polymerase Chain Reaction (PCR) in resistant/intermediate isolates.

Main Results:

  • High rates of imipenem resistance (56%) and intermediate susceptibility (13%) were observed.
  • MBL genes were detected in a significant proportion of resistant/intermediate isolates: vim1 (16.1%), vim2 (2.1%), ipm1 (6.6%), and ipm2 (3.3%).
  • Newer MBL variants were identified, indicating evolving resistance mechanisms.

Conclusions:

  • MBL-mediated imipenem resistance in P. aeruginosa is a growing concern for burn patient treatment.
  • The detection of novel MBL families highlights the increasing prevalence of these resistance genes.
  • Effective interventions are crucial to control MBL production in clinical P. aeruginosa isolates.

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