Molecular features and transmission of NDM-producing Enterobacterales in Israeli hospitals

Author:

Adler Amos12ORCID,Ghosh Hiren3,Gross Andrea3,Rechavi Amit4,Lasnoy Michal1,Assous Marc V5,Geffen Yuval6,Darawshe Basel6,Wiener-Well Yonit78,Grundmann Hajo3,Reuter Sandra3

Affiliation:

1. Clinical Microbiology, Tel Aviv Sourasky Medical Center , Tel Aviv , Israel

2. Department of Epidemiology and Preventative Medicine, School of Public Health, Faculty of Medicine, Tel Aviv University , Tel Aviv , Israel

3. Institute for Infection Prevention and Hospital Epidemiology, Medical Center—University of Freiburg , Freiburg , Germany

4. Ruppin Academic Center , Ruppin , Israel

5. Microbiology Laboratory, Shaare Zedek Medical Center, and the Faculty of Medicine, Hebrew University of Jerusalem , Jerusalem , Israel

6. Rambam Medical Center , Haifa , Israel

7. Infectious Disease Unit, Sha’are Zedek Medical Center , Jerusalem , Israel

8. Faculty of Medicine, Hebrew University of Jerusalem , Jerusalem , Israel

Abstract

AbstractObjectivesNDM-producing Enterobacterales (NDME) account for 34.9% of new carbapenemase-producing Enterobacterales cases in Israeli hospitals. The goals of this study were to characterize the genomic composition of NDME isolates and mobile genetic elements (MGEs) and to identify NDME transmission events (TEs).MethodsThe study was conducted at the Tel-Aviv Sourasky, Rambam and Sha’are-Zedek Medical Centers (TASMC, RMC and SZMC, respectively). All NDME isolates detected between January 2018 and July 2019 were included.Phylogenetic analysis was based on core-genome SNP distances. Core-genome distance of ≤5 SNPs between isolates from patients with overlapping hospitalization periods was suggestive of a potential TE. MGEs were classified by comparison of the blaNDM gene flanking regions.ResultsThe study included 212 NDME isolates from 203 patients, including 104 isolates from TASMC, 30 isolates from RMC and 78 isolates from SZMC. The majority of isolates (n = 157; 74%) harboured the blaNDM-1 gene, followed by the blaNDM-5 (n = 48) and blaNDM-15 genes (n = 7). The most common NDME species were Klebsiella pneumoniae (n = 67), Escherichia coli (n = 65) and Enterobacter cloacae (n = 45), all showing a highly diverse clonal structure. Most blaNDM-1-harbouring isolates (134/157; 85%) were divided into nine different MGE modules, variably distributed across species and hospitals.The numbers of post-admission acquisition cases (n = 118) that could be linked to other cases by both molecular and epidemiological criteria were 13/58 (24.2%), 3/48 (6.3%) and 4/12 (33.3%) in TASMC, SZMC and RMC, respectively.ConclusionsThe study depicted a complex and diverse population structure, suggesting that NDME had not spread via clonal expansion.

Funder

German Israeli Foundation

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Pharmacology (medical),Pharmacology,Microbiology (medical)

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