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Isolation and Identification of Waterborne Antibiotic-Resistant Bacteria and Molecular Characterization of their Antibiotic Resistance Genes
Published on: March 3, 2023
Identification of novel mobile colistin resistance gene mcr-10
Chengcheng Wang1,2,3, Yu Feng1,2,3, Lina Liu3
1Center of Infectious Diseases, West China Hospital, Sichuan University, Chengdu, People's Republic of China.
Abstract:
Mobile colistin resistance (mcr) genes represent an emerging challenge. Here we describe a novel mcr gene, mcr-10, on an IncFIA plasmid of an Enterobacter roggenkampii clinical strain. mcr-10 has the highest nucleotide identity (79.69%) with mcr-9 and encodes MCR-10 with 82.93% amino acids identical to MCR-9. mcr-10 confers 4-fold increase in colistin MIC (from 1 to 4 mg/L) when cloned into a colistin-susceptible E. roggenkampii strain. By screening GenBank, mcr-10 was found in various Enterobacteriaceae species of countries in four continents, suggesting that this gene has widely spread. MCR-10 shows 79.04% to 83.67% amino acid identity and highly conserved predicted protein structures with chromosomally encoded MCR-like phosphoethanolamine transferases (designated MCR-B here) of various Buttiauxella species. MCR-10, MCR-9 and MCR-B proteins may, therefore, originate from a common ancestor. mcr-10 was adjacent to a site-specific recombinase-encoding gene and was bracketed by IS903 and may be mobilized by site-specific recombination or composite transposon. Our results indicate that mcr-10 is a novel plasmid-borne colistin resistance gene and warrants immediate monitoring and further studies.
Insights
A new mobile colistin resistance gene, mcr-10, has been identified on a plasmid in Enterobacter roggenkampii. This gene confers resistance and has already spread globally across various Enterobacteriaceae species.
Area of Science:
- Microbiology
- Genetics
- Antimicrobial Resistance
Background:
- Mobile colistin resistance (mcr) genes pose a significant and growing threat to public health.
- The emergence of new mcr genes necessitates continuous surveillance and characterization.
Purpose of the Study:
- To identify and characterize a novel mobile colistin resistance gene.
- To investigate the prevalence and potential mobilization mechanisms of the new gene.
Main Methods:
- Whole-genome sequencing of an Enterobacter roggenkampii clinical isolate.
- Plasmid analysis and gene cloning into a susceptible strain.
- Bioinformatic screening of public databases (GenBank).
Main Results:
- Discovery of a novel plasmid-borne mcr gene, designated mcr-10, in Enterobacter roggenkampii.
- mcr-10 confers a 4-fold increase in colistin minimum inhibitory concentration (MIC).
- mcr-10 detected across multiple Enterobacteriaceae species on four continents, indicating wide dissemination.
Conclusions:
- mcr-10 represents a novel and concerning mobile colistin resistance gene.
- The gene's association with mobile genetic elements suggests potential for further spread.
- Immediate monitoring and further research on mcr-10 are warranted.
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