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Characterization of NWM-1, a novel subclass B3 metallo-β-lactamase found in a clinical isolate of Pseudomonas aeruginosa. | LitMetric

Characterization of NWM-1, a novel subclass B3 metallo-β-lactamase found in a clinical isolate of Pseudomonas aeruginosa.

J Antimicrob Chemother

German National Reference Centre for Multidrug-resistant Gram-negative Bacteria, Department of Medical Microbiology, Ruhr-University Bochum, Universitätsstraße 150, 44801 Bochum, Germany.

Published: November 2024

AI Article Synopsis

  • The study aimed to understand how a clinical isolate of carbapenem-resistant Pseudomonas aeruginosa resists treatment by investigating its carbapenemase mechanism.
  • Researchers conducted various tests, including phenotypic tests and whole-genome sequencing, to detect and characterize a new metallo-β-lactamase (MBL) gene, named NWM-1, which had not been documented before.
  • The findings emphasize the importance of whole-genome sequencing in discovering new antibiotic resistance mechanisms, highlighting the ongoing evolution of resistance in clinical bacteria.

Article Abstract

Objectives: To investigate the carbapenem resistance mechanism of a carbapenem-resistant clinical Pseudomonas aeruginosa isolate.

Methods: A clinical isolate of P. aeruginosa was sent to the German National Reference Centre for multidrug-resistant Gram-negative bacteria for carbapenemase detection. Phenotypic tests for carbapenemase detection and an EDTA-combined disc test were positive, therefore PCR-screenings were done for the most prevalent metallo-β-lactamase (MBL) encoding genes. As no MBL gene could be found, whole-genome sequencing was performed. For characterization, heterologous expression in a E. coli strain with subsequent MIC testing and purification of the new MBL to determine enzyme kinetics with in vitro hydrolysis assays was performed.

Results: WGS revealed the putative gene for a B3 MBL located on the chromosome between several disrupted IS elements with 67% identity to EVM-1, which was named NWM-1. MIC studies and enzyme kinetics confirmed MBL activity. No activity against ceftazidime was observed.

Conclusions: The identification of NWM-1 shows the importance of WGS to identify yet unknown carbapenemases and underlines the diversity of subclass B3 β-lactamases. It also shows that although several carbapenemase variants have already been identified and characterized, there are always new variants to be found in clinical isolates.

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Source
http://dx.doi.org/10.1093/jac/dkae428DOI Listing

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