Characterization of the Plasmidome Encoding Carbapenemase and Mechanisms for Dissemination of Carbapenem-Resistant Enterobacteriaceae

Author:

Abe Ryuichiro12,Akeda Yukihiro134ORCID,Sugawara Yo1ORCID,Takeuchi Dan1,Matsumoto Yuki5,Motooka Daisuke5,Yamamoto Norihisa123,Kawahara Ryuji6,Tomono Kazunori34,Fujino Yuji2,Hamada Shigeyuki1

Affiliation:

1. Japan-Thailand Research Collaboration Centre on Emerging and Re-emerging Infections, Research Institute for Microbial Diseases, Osaka University, Osaka, Japan

2. Department of Anaesthesiology and Intensive Care Medicine, Graduate School of Medicine, Osaka University, Osaka, Japan

3. Division of Infection Control and Prevention, Osaka University Hospital, Osaka, Japan

4. Division of Infection Control and Prevention, Graduate School of Medicine, Osaka University, Osaka, Japan

5. Department of Infection Metagenomics, Research Institute for Microbial Diseases, Osaka University, Osaka, Japan

6. Department of Microbiology, Osaka Institute of Public Health, Osaka, Japan

Abstract

Global dissemination of carbapenem-resistant Enterobacteriaceae (CRE) threatens human health by limiting the efficacy of antibiotics even against common bacterial infections. Carbapenem resistance, mainly due to carbapenemase, is generally encoded on plasmids and is spread across bacterial species by conjugation. Most CRE epidemiological studies have analyzed whole genomes or only contigs of CRE isolates. Here, plasmidome analysis on 230 CRE isolates carrying bla IMP was performed to shed light into the dissemination of a single carbapenemase gene in Osaka, Japan. The predominant dissemination of bla IMP-6 by the pKPI-6 plasmid among genetically distinct isolates was revealed, as well as the emergences of pKPI-6 derivatives that acquired advantages for further disseminations. Underlying vast clonal dissemination of a carbapenemase-encoding plasmid, heteroresistance was found in CRE offspring, which was generated by the transcriptional regulation of bla IMP-6 , stabilization of bla IMP-6 through chromosomal integration, or broadened antimicrobial resistance due to a single point mutation in bla IMP-6 .

Funder

Japan Agency for Medical Research and Development

Publisher

American Society for Microbiology

Subject

Computer Science Applications,Genetics,Molecular Biology,Modelling and Simulation,Ecology, Evolution, Behavior and Systematics,Biochemistry,Physiology,Microbiology

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