Clonal outbreak of NDM-1-producing Enterobacter hormaechei belonging to high-risk international clone ST78 with the coexistence of tmexCD2-toprJ2 and mcr-9 in China

Int J Antimicrob Agents. 2023 Jun;61(6):106790. doi: 10.1016/j.ijantimicag.2023.106790. Epub 2023 Mar 15.

Abstract

Objectives: The emergence of carbapenem-resistant Enterobacter cloacae complex (CR-ECC) has posed significant global challenges to the clinical treatment of healthcare-associated infections. This study reports the clonal outbreak of NDM-1-producing Enterobacter hormaechei (E. hormaechei) with the coexistence of tmexCD2-toprJ2 and mcr-9 in China.

Methods: During the outbreak (January 2018 - December 2021), 15 non-repetitive multidrug-resistant E. hormaechei strains were obtained from 13 patients in a tertiary hospital. Antimicrobial susceptibility testing, plasmid stability, plasmid conjugation, plasmid fitness evaluation, colistin induction, whole-genome sequencing, and bioinformatics analysis were performed. A phylogenetic tree was constructed based on single nucleotide polymorphisms of core genomes to illustrate the evolutionary dynamics of mcr-9-carrying E. hormaechei strains worldwide.

Results: The 15 E. hormaechei strains belonged to the high-risk international clone ST78 and co-harboured tmexCD2-toprJ2 and blaNDM-1, of which 12 E. hormaechei strains carried the mcr-9 gene. Whole-genome sequencing analysis revealed that tmexCD2-toprJ2 and blaNDM-1 coexisted on the IncFIB/IncFII-type plasmid, which could be transferred to Escherichia coli J53 by conjugation and had a significant effect on host fitness. The mcr-9 gene was located between two insertion sequences, IS903B and IS1R, but lacked the two-component system regulatory gene qseBC, which might be the reason for all mcr-9-positive E. hormaechei strains remaining susceptible to colistin. The expression of mcr-9 was not inducible in strains confirmed by colistin induction assays. Phylogenetic analysis illustrated the silent spread and rapid evolution of mcr-9-carrying E. hormaechei worldwide.

Conclusion: This study enriched the epidemiological and genomic characterisation of the coexistence of tmexCD2-toprJ2 and mcr-9 in ST78 CR-ECC isolates and demonstrated that they could prolong clonal dissemination in a tertiary hospital in China. Continuous epidemiological surveillance and molecular characterisation of CR-ECC should be conducted to monitor the evolution of CR-ECC around the world.

Keywords: Carbapenem-resistant Enterobacter cloacae complex (CR-ECC); Clonal transmission; Enterobacter hormaechei; bla(NDM-1), tmexCD2-toprJ2, mcr-9.

MeSH terms

  • Anti-Bacterial Agents / pharmacology
  • China / epidemiology
  • Colistin* / pharmacology
  • Escherichia coli
  • Humans
  • Microbial Sensitivity Tests
  • Phylogeny
  • Plasmids / genetics
  • beta-Lactamases* / metabolism

Substances

  • beta-lactamase NDM-1
  • Colistin
  • beta-Lactamases
  • Anti-Bacterial Agents

Supplementary concepts

  • Enterobacter hormaechei