Emergence of NDM-1-Producing Pseudomonas aeruginosa Nosocomial Isolates in Attica Region of Greece

Author:

Pappa Olga1,Louka Christina2,Karadimas Kleon1,Maikousi Evangelia1,Tzoukmani Angeliki1,Polemis Michalis1,Panopoulou Anna-Danai3,Daniil Ioannis2ORCID,Chryssou Stella3,Mellou Kassiani4ORCID,Kjeldgaard Jette S.5,Zarkotou Olympia2,Papagiannitsis Costas6ORCID,Tryfinopoulou Kyriaki17ORCID

Affiliation:

1. AMR and HAIs Laboratory, Central Public Health Laboratory, National Public Health Organization, Vari, 16672 Attica, Greece

2. Clinical Microbiology Laboratory, Tzaneion General Hospital of Piraeus, 18536 Attica, Greece

3. Clinical Microbiology Laboratory, Syggros Hospital of Athens, 16121 Attica, Greece

4. Directorate of Epidemiological Surveillance and Response for Infectious Diseases, National Public Health Organization, 15123 Athens, Greece

5. European Union Reference Laboratory for Antimicrobial Resistance (EURL-AR), National Food Institute, Technical University of Denmark, 2800 Kongens Lyngby, Denmark

6. Department of Microbiology, University Hospital of Larissa, 41334 Larissa, Greece

7. Clinical Microbiology and Microbial Pathogenesis Laboratory, School of Medicine, University of Crete, Heraklion, 71500 Crete, Greece

Abstract

Here, we report on the emergence and spread of multidrug-resistant NDM-1-producing P. aeruginosa isolates from patients hospitalized in the Attica region, Greece, in 2022 to provide data on their resistome, their virulome, the genetic environment of blaNDM-1, and their molecular epidemiology. A total of 17 carbapenem-resistant P. aeruginosa isolates identified as NDM-producers by immunochromatography at the hospital level were sent to the Central Public Health Laboratory, in the frame of the laboratory surveillance of carbapenem-resistant pathogens, for further characterization. The initial screening for genetic AMR determinants was carried out by PCR and the MDR Direct Flow Chip assay. Typing was performed by MLST and DLST, the latter in a subset of isolates. Further analysis was performed by whole-genome sequencing (WGS) of six isolates from both hospitals to analyze their entire genomes and elucidate their genetic relatedness. All isolates were allocated to international high-risk clones, sixteen to ST773 and one to ST308. Five ST773 and the sole ST308 isolate were found to harbor the blaNDM-1 gene, along with various other ARGs integrated into their chromosomes, as well as with a wide variety of virulence genes. The blaNDM-1 gene was located in the integrative and conjugative elements ICE6600-like and ICETn43716385 in ST773 and ST308 isolates, respectively. Single-nucleotide polymorphism analysis of the five ST773 isolates indicated their clonal spread in both hospitals. These results suggested that two different molecular events contributed to the emergence of NDM-1-producing P. aeruginosa isolates in Athenian hospitals, highlighting the need for ongoing surveillance.

Publisher

MDPI AG

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