Emergence and transmission of the high-risk ST78 clone of OXA-48-producing Enterobacter hormaechei in a single hospital in Taiwan

Emerg Microbes Infect. 2024 Dec;13(1):2404165. doi: 10.1080/22221751.2024.2404165. Epub 2024 Sep 22.

Abstract

Carbapenem-resistant Enterobacter cloacae complex is a significant global healthcare threat, particularly carbapenemase-producing Enterobacter hormaechei (CPEH). From January 2017 to January 2021, twenty-two CPEH isolates from a regional teaching hospital in central Taiwan were identified with the carriage of carbapenemase genes blaKPC-2, blaIMP-8, and predominantly blaOXA-48. Over 80% of these CPEH strains clustered into the high-risk ST78 lineage, carrying a blaOXA-48 IncL plasmid (pOXA48-CREH), nearly identical to the endemic plasmid pOXA48-KP in ST11 Klebsiella pneumoniae. This OXA-48-producing ST78 lineage disseminated clonally from 2018 to 2021 and transferred pOXA48-CREH to ST66 and ST90 E. hormaechei. An IMP-8-producing ST78 strain harbouring a blaIMP-8-carrying pIncHI2 plasmid appeared in 2018, and by late 2020, a KPC-2-producing ST78 strain was identified after acquiring a novel blaKPC-2-carrying IncFII plasmid. These findings suggest that the high-risk ST78 lineage of E. hormaechei has emerged as the primary driver behind the transmission of CPEH. ST78 has not only acquired various carbapenemase-gene-carrying plasmids but has also facilitated the transfer of pOXA48-CREH to other lineages. Continuous genomic surveillance and targeted interventions are urgently needed to control the spread of emerging CPEH clones in hospital settings.

Keywords: Carbapenemase genes; Enterobacter hormaechei; OXA-48; ST78; mcr-9.1; plasmidome; resistome.

MeSH terms

  • Anti-Bacterial Agents / pharmacology
  • Bacterial Proteins* / genetics
  • Bacterial Proteins* / metabolism
  • Carbapenem-Resistant Enterobacteriaceae / genetics
  • Carbapenem-Resistant Enterobacteriaceae / isolation & purification
  • Enterobacter* / drug effects
  • Enterobacter* / enzymology
  • Enterobacter* / genetics
  • Enterobacter* / isolation & purification
  • Enterobacteriaceae Infections* / epidemiology
  • Enterobacteriaceae Infections* / microbiology
  • Enterobacteriaceae Infections* / transmission
  • Hospitals
  • Humans
  • Microbial Sensitivity Tests
  • Plasmids* / genetics
  • Taiwan / epidemiology
  • beta-Lactamases* / genetics
  • beta-Lactamases* / metabolism

Substances

  • beta-Lactamases
  • Bacterial Proteins
  • Anti-Bacterial Agents
  • carbapenemase
  • oxacillinase

Supplementary concepts

  • Enterobacter hormaechei

Grants and funding

This work was supported by National Chung Hsing University and Chung Shan Medical University, Taichung, Taiwan [grant no NCHU-CSMU-10702], China Medical University Hospital, Taichung, Taiwan [grant no DMR-111-040], and Tungs' Taichung MetroHarbor Hospital [grant no TTMHH-109R0041]. The funders had no role in the study design, data collection, analysis, publication decision, or manuscript preparation.