<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>43(3)</volume><submitter>Findlay J</submitter><funding>University of Fribourg</funding><pubmed_abstract>&lt;h4>Objectives&lt;/h4>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.&lt;h4>Methods&lt;/h4>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, bla&lt;sub>NDM-1&lt;/sub>, bla&lt;sub>IMP-1&lt;/sub>, and bla&lt;sub>VIM-2&lt;/sub>, were cloned into vector pUCP24 and transformed into P. aeruginosa PA14.&lt;h4>Results&lt;/h4>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 bla&lt;sub>NDM-1&lt;/sub>, bla&lt;sub>IMP-1&lt;/sub>, and bla&lt;sub>VIM-2&lt;/sub> exhibited FDC MICs of 16, 8, and 1 mg/L, respectively.&lt;h4>Conclusions&lt;/h4>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.</pubmed_abstract><journal>European journal of clinical microbiology &amp; infectious diseases : official publication of the European Society of Clinical Microbiology</journal><pagination>551-557</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10917820</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Molecular analysis of metallo-beta-lactamase-producing Pseudomonas aeruginosa in Switzerland 2022-2023.</pubmed_title><pmcid>PMC10917820</pmcid><pubmed_authors>Lemaire B</pubmed_authors><pubmed_authors>Monnerat LB</pubmed_authors><pubmed_authors>Boschung D</pubmed_authors><pubmed_authors>Fankhauser H</pubmed_authors><pubmed_authors>Greub G</pubmed_authors><pubmed_authors>Dubois O</pubmed_authors><pubmed_authors>Moraz M</pubmed_authors><pubmed_authors>Pranghofer S</pubmed_authors><pubmed_authors>Casanova C</pubmed_authors><pubmed_authors>Elzi M</pubmed_authors><pubmed_authors>Pfister S</pubmed_authors><pubmed_authors>Guler C</pubmed_authors><pubmed_authors>Menozzi FB</pubmed_authors><pubmed_authors>Goldenberger D</pubmed_authors><pubmed_authors>Emonet S</pubmed_authors><pubmed_authors>Hitz E</pubmed_authors><pubmed_authors>Narr K</pubmed_authors><pubmed_authors>Pozzi L</pubmed_authors><pubmed_authors>Liassine N</pubmed_authors><pubmed_authors>Mathis B</pubmed_authors><pubmed_authors>Raro OHF</pubmed_authors><pubmed_authors>Bandeira D</pubmed_authors><pubmed_authors>Cirillo C</pubmed_authors><pubmed_authors>Suterbuser B</pubmed_authors><pubmed_authors>Staehli P</pubmed_authors><pubmed_authors>Keller P</pubmed_authors><pubmed_authors>Jayol A</pubmed_authors><pubmed_authors>Schmid S</pubmed_authors><pubmed_authors>Schultze D</pubmed_authors><pubmed_authors>Oberle M</pubmed_authors><pubmed_authors>Scherler A</pubmed_authors><pubmed_authors>Herzog K</pubmed_authors><pubmed_authors>Mitrovic I</pubmed_authors><pubmed_authors>Vonallmen L</pubmed_authors><pubmed_authors>Schmid T</pubmed_authors><pubmed_authors>Wohlwend N</pubmed_authors><pubmed_authors>Graf S</pubmed_authors><pubmed_authors>Burren K</pubmed_authors><pubmed_authors>Lienhard R</pubmed_authors><pubmed_authors>Payen C</pubmed_authors><pubmed_authors>NARA Network</pubmed_authors><pubmed_authors>Imhof A</pubmed_authors><pubmed_authors>Jutzi M</pubmed_authors><pubmed_authors>Fournier C</pubmed_authors><pubmed_authors>Poirel L</pubmed_authors><pubmed_authors>Dubey N</pubmed_authors><pubmed_authors>Vitale A</pubmed_authors><pubmed_authors>Maitrejean M</pubmed_authors><pubmed_authors>Findlay J</pubmed_authors><pubmed_authors>Fricker C</pubmed_authors><pubmed_authors>Blanc D</pubmed_authors><pubmed_authors>Maret R</pubmed_authors><pubmed_authors>Kuegler M</pubmed_authors><pubmed_authors>Marti CO</pubmed_authors><pubmed_authors>Schoenenberger M</pubmed_authors><pubmed_authors>Lucke K</pubmed_authors><pubmed_authors>Rumebe L</pubmed_authors><pubmed_authors>Basilico L</pubmed_authors><pubmed_authors>Schoch S</pubmed_authors><pubmed_authors>Droz S</pubmed_authors><pubmed_authors>Hyden D</pubmed_authors><pubmed_authors>Lang C</pubmed_authors><pubmed_authors>Schnell B</pubmed_authors><pubmed_authors>Schibli U</pubmed_authors><pubmed_authors>Born Y</pubmed_authors><pubmed_authors>Andreutti C</pubmed_authors><pubmed_authors>Togni G</pubmed_authors><pubmed_authors>Imperiali M</pubmed_authors><pubmed_authors>Piran F</pubmed_authors><pubmed_authors>Bruderer V</pubmed_authors><pubmed_authors>Westers A</pubmed_authors><pubmed_authors>Zowa C</pubmed_authors><pubmed_authors>Belo A</pubmed_authors><pubmed_authors>Gruner E</pubmed_authors><pubmed_authors>Fatoux M</pubmed_authors><pubmed_authors>Guyon C</pubmed_authors><pubmed_authors>Jost G</pubmed_authors><pubmed_authors>Vaninetti G</pubmed_authors><pubmed_authors>Seiffert S</pubmed_authors><pubmed_authors>Balzari D</pubmed_authors><pubmed_authors>Castelberg C</pubmed_authors><pubmed_authors>Egli A</pubmed_authors><pubmed_authors>Gisler V</pubmed_authors><pubmed_authors>Steffen I</pubmed_authors><pubmed_authors>Pianezzi E</pubmed_authors><pubmed_authors>Deggi-Messmer V</pubmed_authors><pubmed_authors>Andrey D</pubmed_authors><pubmed_authors>Tritten M</pubmed_authors><pubmed_authors>Povolo V</pubmed_authors><pubmed_authors>Ellenberger S</pubmed_authors><pubmed_authors>Renzi G</pubmed_authors><pubmed_authors>Nusbaumer C</pubmed_authors><pubmed_authors>Brandenberger M</pubmed_authors><pubmed_authors>Zehnder C</pubmed_authors><pubmed_authors>Lucchini GM</pubmed_authors><pubmed_authors>Cherkaoui A</pubmed_authors><pubmed_authors>Schrenzel J</pubmed_authors><pubmed_authors>Dilorenzo V</pubmed_authors><pubmed_authors>Nordmann P</pubmed_authors><pubmed_authors>Preiswerk B</pubmed_authors><pubmed_authors>Comte L</pubmed_authors><pubmed_authors>Schilt C</pubmed_authors><pubmed_authors>Ivan B</pubmed_authors><pubmed_authors>Karrer U</pubmed_authors><pubmed_authors>Dessauges M</pubmed_authors><pubmed_authors>Mancini S</pubmed_authors><pubmed_authors>Blaich A</pubmed_authors><pubmed_authors>Reichmuth M</pubmed_authors><pubmed_authors>Gaia V</pubmed_authors><pubmed_authors>Mabillard D</pubmed_authors><pubmed_authors>Eyer M</pubmed_authors><pubmed_authors>Minkova P</pubmed_authors><pubmed_authors>Schacher M</pubmed_authors></additional><is_claimable>false</is_claimable><name>Molecular analysis of metallo-beta-lactamase-producing Pseudomonas aeruginosa in Switzerland 2022-2023.</name><description>&lt;h4>Objectives&lt;/h4>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.&lt;h4>Methods&lt;/h4>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, bla&lt;sub>NDM-1&lt;/sub>, bla&lt;sub>IMP-1&lt;/sub>, and bla&lt;sub>VIM-2&lt;/sub>, were cloned into vector pUCP24 and transformed into P. aeruginosa PA14.&lt;h4>Results&lt;/h4>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 bla&lt;sub>NDM-1&lt;/sub>, bla&lt;sub>IMP-1&lt;/sub>, and bla&lt;sub>VIM-2&lt;/sub> exhibited FDC MICs of 16, 8, and 1 mg/L, respectively.&lt;h4>Conclusions&lt;/h4>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.</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Mar</publication><modification>2026-06-09T07:09:04.161Z</modification><creation>2025-04-07T02:10:05.692Z</creation></dates><accession>S-EPMC10917820</accession><cross_references><pubmed>38233610</pubmed><doi>10.1007/s10096-024-04752-8</doi></cross_references></HashMap>