Potential Mobilization of mcr-10 by an Integrative Mobile Element via Site-Specific Recombination in Cronobacter

Jing Yang1,2,3, Lina Liu4, Yu Feng1,3,4

  • 1Center of Infectious Diseases, West China Hospital, Sichuan University, Chengdu, China.

Insights

The newly discovered mcr-10 colistin resistance gene

Area of Science:

  • Microbiology
  • Genetics
  • Molecular Biology

Background:

  • The mcr-10 gene confers resistance to colistin, a crucial antibiotic.
  • The mechanism of mcr-10 gene spread is not well understood.
  • Cronobacter sakazakii is an opportunistic pathogen.

Purpose of the Study:

  • To investigate the mobilization mechanism of the mcr-10 gene.
  • To identify the genetic context of mcr-10 in a Cronobacter sakazakii isolate.

Main Methods:

  • Plasmid analysis
  • Comparative genomics
  • Identification of recombination sites

Main Results:

  • The mcr-10 gene was located on an IncFIB plasmid in Cronobacter sakazakii.
  • This plasmid also carried virulence genes: mrkABCDFJ, iucABCD/iutA, and eitCBAD.
  • Two recombination sites flanking the mcr-10 genetic element were identified.

Conclusions:

  • Site-specific recombination mediated by an integrase is a likely mechanism for mcr-10 mobilization.
  • Understanding mcr-10 mobilization is critical for controlling antibiotic resistance spread.

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