Emergence of Plasmid-mediated Colistin Resistance Mechanism MCR-1 in Animals and Human Beings in China: a Microbiological and Molecular Biological Study
Overview
Authors
Affiliations
Background: Until now, polymyxin resistance has involved chromosomal mutations but has never been reported via horizontal gene transfer. During a routine surveillance project on antimicrobial resistance in commensal Escherichia coli from food animals in China, a major increase of colistin resistance was observed. When an E coli strain, SHP45, possessing colistin resistance that could be transferred to another strain, was isolated from a pig, we conducted further analysis of possible plasmid-mediated polymyxin resistance. Herein, we report the emergence of the first plasmid-mediated polymyxin resistance mechanism, MCR-1, in Enterobacteriaceae.
Methods: The mcr-1 gene in E coli strain SHP45 was identified by whole plasmid sequencing and subcloning. MCR-1 mechanistic studies were done with sequence comparisons, homology modelling, and electrospray ionisation mass spectrometry. The prevalence of mcr-1 was investigated in E coli and Klebsiella pneumoniae strains collected from five provinces between April, 2011, and November, 2014. The ability of MCR-1 to confer polymyxin resistance in vivo was examined in a murine thigh model.
Findings: Polymyxin resistance was shown to be singularly due to the plasmid-mediated mcr-1 gene. The plasmid carrying mcr-1 was mobilised to an E coli recipient at a frequency of 10(-1) to 10(-3) cells per recipient cell by conjugation, and maintained in K pneumoniae and Pseudomonas aeruginosa. In an in-vivo model, production of MCR-1 negated the efficacy of colistin. MCR-1 is a member of the phosphoethanolamine transferase enzyme family, with expression in E coli resulting in the addition of phosphoethanolamine to lipid A. We observed mcr-1 carriage in E coli isolates collected from 78 (15%) of 523 samples of raw meat and 166 (21%) of 804 animals during 2011-14, and 16 (1%) of 1322 samples from inpatients with infection.
Interpretation: The emergence of MCR-1 heralds the breach of the last group of antibiotics, polymyxins, by plasmid-mediated resistance. Although currently confined to China, MCR-1 is likely to emulate other global resistance mechanisms such as NDM-1. Our findings emphasise the urgent need for coordinated global action in the fight against pan-drug-resistant Gram-negative bacteria.
Funding: Ministry of Science and Technology of China, National Natural Science Foundation of China.
Zhai W, Wang Y, Sun H, Fu B, Zhang Q, Wu C Biosaf Health. 2025; 6(2):116-124.
PMID: 40078945 PMC: 11895030. DOI: 10.1016/j.bsheal.2024.02.004.
Yu Y, He Z, Wang C Front Cell Infect Microbiol. 2025; 15:1533177.
PMID: 40078873 PMC: 11897560. DOI: 10.3389/fcimb.2025.1533177.
Yadav K, Datkhile K, Pawar S, Patil S Cureus. 2025; 17(2):e78800.
PMID: 40078264 PMC: 11902915. DOI: 10.7759/cureus.78800.
Aswal M, Singh N, Singhal N, Kumar M Front Microbiol. 2025; 16:1531739.
PMID: 40071204 PMC: 11893563. DOI: 10.3389/fmicb.2025.1531739.
Xie M, Zhang Y, Chen K, Dong N, Zhou H, Huang Y Commun Med (Lond). 2025; 5(1):73.
PMID: 40069403 PMC: 11897290. DOI: 10.1038/s43856-025-00748-3.