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Updated: Nov 30, 2025

Site-specific Bacterial Chromosome Engineering: ΦC31 Integrase Mediated Cassette Exchange (IMCE)
Published on: March 16, 2012
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.
Abstract:
mcr-10 is a newly identified plasmid-borne colistin resistance gene, but its mobilization mechanism remains unclear. In this study, mcr-10 was found on an IncFIB plasmid carrying virulence genes mrkABCDFJ, iucABCD/iutA, and eitCBAD in a Cronobacter sakazakii isolate. By comparison with closely related plasmids, two recombination sites were identified flanking the genetic element containing mcr-10 and an integrase-encoding gene, suggesting that site-specific recombination mediated by an integrase of an integrative mobile element is a potential mechanism for mobilizing mcr-10.
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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