Identification of AbaR4 Acinetobacter baumannii resistance island in clinical isolates of blaOXA-23-positive Proteus mirabilis

Author:

Octavia Sophie12,Xu Weizhen23,Ng Oon Tek1234,Marimuthu Kalisvar235ORCID,Venkatachalam Indumathi6,Cheng Bernadette7,Lin Raymond T P127,Teo Jeanette W P7ORCID

Affiliation:

1. National Public Health Laboratory, Ministry of Health, Singapore

2. National Centre for Infectious Diseases, Singapore

3. Tan Tock Seng Hospital, Department of Infectious Diseases, Singapore

4. Nanyang Technological University, Lee Kong Chian School of Medicine, Singapore

5. National University of Singapore, Yong Loo Lin School of Medicine, Singapore

6. Singapore General Hospital, Department of Infectious Diseases and Department of Infection Prevention & Epidemiology, Singapore

7. National University Hospital, Department of Laboratory Medicine, Singapore

Abstract

Abstract Objectives bla OXA-23 is a class D carbapenemase-encoding gene typical of the Acinetobacter genus. However, its occurrence in the Enterobacteriaceae is uncommon. Here we provide the genome characterization of blaOXA-23-positive Proteus mirabilis. Methods In Singapore, a national surveillance of carbapenem non-susceptible clinical Enterobacteriaceae has enabled the collection of OXA-23 bearing isolates. Three clinical P. mirabilis were whole-genome sequenced using Oxford Nanopore MinION and Illumina platforms. The sequence accuracy of MinION long-read contigs was enhanced by polishing with Illumina-derived short-read data. Results In two P. mirabilis genomes, blaOXA-23 was detected as two copies, present on the chromosome and on a 60018 bp plasmid. blaOXA-23 was associated with the classic Acinetobacter composite transposon Tn2006, bounded by two copies of ISAba1 bracketing the carbapenemase gene. The Tn2006 itself was embedded within an Acinetobacter baumannii AbaR4 resistance island. In the chromosome, the AbaR4 was found integrated into the comM gene, which is also the preferred ‘hotspot’ in A. baumannii. In the plasmid, AbaR4 integrated into a putative colicin gene. Conclusions Our description of an A. baumannii AbaR4 encoding blaOXA-23 in P. mirabilis is to our knowledge the first description of an Acinetobacter resistance island in Proteus and suggests that P. mirabilis may be a reservoir for this class D carbapenemase gene.

Funder

National Medical Research Council

NMRC

Clinician-Scientist Individual Research

Singapore Ministry of Education Academic Research Fund Tier 2

NMRC Collaborative Grant

Collaborative Solutions Targeting Antimicrobial Resistance Threats in Health Systems

NMRC Clinician Scientist Award

Publisher

Oxford University Press (OUP)

Subject

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

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