Chromosomally Encoded mcr-5 in Colistin-Nonsusceptible Pseudomonas aeruginosa

Erik Snesrud1, Rosslyn Maybank1, Yoon I Kwak1

  • 1Multi-drug Resistant Organism Repository and Surveillance Network, Walter Reed Army Institute of Research, Silver Spring, Maryland, USA.

Insights

Whole-genome sequencing identified the mcr-5 gene in a colistin-nonsusceptible Pseudomonas aeruginosa isolate. This discovery marks the first report of mcr-5 in this bacterium, highlighting a new challenge in antimicrobial resistance.

Area of Science:

  • Microbiology
  • Genomics
  • Antimicrobial Resistance

Background:

  • Pseudomonas aeruginosa is an opportunistic pathogen known for its intrinsic resistance to antibiotics.
  • Colistin is a last-resort antibiotic used to treat infections caused by multidrug-resistant Gram-negative bacteria.
  • The emergence of colistin resistance mechanisms is a significant global health concern.

Purpose of the Study:

  • To investigate the genetic basis of colistin nonsusceptibility in a historical Pseudomonas aeruginosa clinical isolate.
  • To identify novel resistance determinants in P. aeruginosa.

Main Methods:

  • Whole-genome sequencing (WGS) was performed on a historical P. aeruginosa clinical isolate (MRSN 12280).
  • Broth microdilution was used to determine colistin susceptibility.
  • Bioinformatic analysis was conducted to identify resistance genes and mutations.

Main Results:

  • A chromosomal copy of the mcr-5 gene, located within a Tn3-like transposon, was identified in P. aeruginosa MRSN 12280.
  • The isolate exhibited nonsusceptibility to colistin.
  • No previously known mutations conferring colistin resistance were found in the isolate's genome.

Conclusions:

  • This study reports the first instance of the mcr-5 gene in a colistin-nonsusceptible P. aeruginosa isolate.
  • The presence of mcr-5 in P. aeruginosa represents a novel mechanism of colistin resistance, potentially complicating treatment strategies.
  • Further research is needed to understand the prevalence and clinical implications of mcr-5 in P. aeruginosa.

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