Pseudomonas aeruginosa Clinical Isolates in Nepal Coproducing Metallo-β-Lactamases and 16S rRNA Methyltransferases

Tatsuya Tada1,2, Kayo Shimada3, Kazuhito Satou4

  • 1Department of Infectious Diseases, Research Institute, National Center for Global Health and Medicine, Tokyo, Japan ttada@ri.ncgm.go.jp.

Insights

Multidrug-resistant Pseudomonas aeruginosa isolates in Nepal carry carbapenemase and 16S rRNA methyltransferase genes. This study identifies novel resistance mechanisms, including a new RmtF variant, in these critical clinical pathogens.

Area of Science:

  • Medical Microbiology
  • Infectious Diseases
  • Antimicrobial Resistance

Background:

  • Multidrug-resistant (MDR) Pseudomonas aeruginosa poses a significant global health threat.
  • Carbapenemases and 16S rRNA methyltransferases are key mechanisms of antibiotic resistance.
  • Limited data exists on the co-occurrence of these resistance genes in P. aeruginosa from Nepal.

Purpose of the Study:

  • To investigate the prevalence of carbapenemase and 16S rRNA methyltransferase genes in MDR P. aeruginosa clinical isolates from Nepal.
  • To characterize novel resistance gene variants identified in these isolates.

Main Methods:

  • Phenotypic and genotypic analysis of 11 MDR P. aeruginosa clinical isolates.
  • Detection of carbapenemase genes (e.g., blaDIM, blaNDM, blaVIM) using molecular methods.
  • Identification of 16S rRNA methyltransferase genes (e.g., rmtB, rmtF) and sequencing for variant analysis.

Main Results:

  • Four out of 11 isolates harbored carbapenemase genes (DIM-1, NDM-1, VIM-2).
  • Five isolates carried 16S rRNA methyltransferase genes (RmtB4, RmtF2).
  • A novel variant, RmtF2, with a K65E substitution, was identified.

Conclusions:

  • This is the first report of carbapenemase- and 16S rRNA methyltransferase-co-producing P. aeruginosa clinical isolates in Nepal.
  • The findings highlight the emergence of complex antibiotic resistance mechanisms in this region.
  • Continuous surveillance is crucial to monitor and combat the spread of MDR pathogens.