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Molecular analysis of metallo-beta-lactamase-producing Pseudomonas aeruginosa in Switzerland 2022–2023

  • Jacqueline Findlay,
  • Otavio Hallal Ferreira Raro,
  • Laurent Poirel,
  • Patrice Nordmann,
  • R. Lienhard,
  • L. Vonallmen,
  • C. Schilt,
  • A. Scherler,
  • K. Lucke,
  • M. Jutzi,
  • M. Reichmuth,
  • U. Schibli,
  • C. Fricker,
  • S. Pranghofer,
  • G. Greub,
  • D. Blanc,
  • A. Vitale,
  • B. Lemaire,
  • M. Fatoux,
  • M. Tritten,
  • L. Rumebe,
  • N. Liassine,
  • G. Jost,
  • N. Wohlwend,
  • D. Schultze,
  • K. Burren,
  • A. Westers,
  • M. Imperiali,
  • L. Pozzi,
  • D. Balzari,
  • G. Vaninetti,
  • C. Cirillo,
  • V. Gaia,
  • E. Pianezzi,
  • G. Martinetti Lucchini,
  • F. Baggi Menozzi,
  • A. Jayol,
  • C. Guyon,
  • D. Hyden,
  • M. Maitrejean,
  • V. Deggi-Messmer,
  • D. Bandeira,
  • C. Fournier,
  • S. Pfister,
  • C. Nusbaumer,
  • L. Bertaiola Monnerat,
  • J. Schrenzel,
  • G. Renzi,
  • A. Cherkaoui,
  • D. Andrey,
  • S. Emonet,
  • M. Eyer,
  • R. Maret,
  • A. Belo,
  • D. Mabillard,
  • M. Moraz,
  • K. Herzog,
  • V. Gisler,
  • E. Hitz,
  • M. Oberle,
  • C. Castelberg,
  • H. Fankhauser,
  • S. Graf,
  • N. Dubey,
  • C. Guler,
  • M. Schoenenberger,
  • U. Karrer,
  • F. Piran,
  • C. Andreutti,
  • M. Dessauges,
  • T. Schmid,
  • B. Suterbuser,
  • I. Mitrovic,
  • E. Gruner,
  • V. Bruderer,
  • P. Staehli,
  • B. Schnell,
  • C. O. Marti,
  • I. Steffen,
  • A. Imhof,
  • B. Preiswerk,
  • V. Dilorenzo,
  • C. Payen,
  • D. Boschung,
  • L. Comte,
  • M. Schacher,
  • M. Brandenberger,
  • C. Zowa,
  • C. Zehnder,
  • B. Mathis,
  • L. Basilico,
  • G. Togni,
  • P. Minkova,
  • Y. Born,
  • M. Kuegler,
  • V. Povolo,
  • S. Droz,
  • M. Elzi,
  • C. Casanova,
  • D. Goldenberger,
  • P. Keller,
  • C. Lang,
  • A. Blaich,
  • S. Schmid,
  • B. Ivan,
  • A. Egli,
  • S. Mancini,
  • O. Dubois,
  • K. Narr,
  • S. Schoch,
  • S. Ellenberger,
  • S. Seiffert

摘要

Objectives

The occurrence of metallo-beta-lactamase-producing Pseudomonas aeruginosa (MBL-PA) isolates is increasing globally, including in Switzerland. The aim of this study was to characterise, phenotypically and genotypically, the MBL-PA isolates submitted to the Swiss National Reference Center for Emerging Antibiotic Resistance (NARA) reference laboratory over a 12-month period from July 2022 to July 2023.

Methods

Thirty-nine non-duplicate MBL-PA Isolates were submitted to NARA over the study period from across Switzerland. Susceptibility was determined by broth microdilution according to EUCAST methodology. Whole-genome sequencing was performed on 34 isolates. Sequence types (STs) and resistance genes were ascertained using the Centre for Genomic Epidemiology platform. MBL genes, blaNDM-1, blaIMP-1, and blaVIM-2, were cloned into vector pUCP24 and transformed into P. aeruginosa PA14.

Results

The most prevalent MBL types identified in this study were VIM (21/39; 53.8%) followed by NDM (11/39; 28.2%), IMP (6/39; 15.4%), and a single isolate produced both VIM and NDM enzymes. WGS identified 13 different STs types among the 39 isolates. They all exhibited resistance to cephalosporins, carbapenems, and the beta-lactam-beta-lactamase inhibitor combinations, ceftolozane-tazobactam, ceftazidime-avibactam, imipenem-relebactam, and meropenem-vaborbactam, and 8 isolates were cefiderocol (FDC) resistant. Recombinant P. aeruginosa strains producing blaNDM-1, blaIMP-1, and blaVIM-2 exhibited FDC MICs of 16, 8, and 1 mg/L, respectively.

Conclusions

This study showed that the MBL-PA in Switzerland could be attributed to the wide dissemination of high-risk clones that accounted for most isolates in this study. Although FDC resistance was only found in 8 isolates, MBL carriage was shown to be a major contributor to this phenotype.