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Updated: Feb 13, 2026

Following the Dynamics of Structural Variants in Experimentally Evolved Populations
Published on: February 3, 2023
mcr gene family evolution and structural mechanisms of colistin resistance: from mcr-1 to emerging variants
Muhammad Shahid Mehmood1, Uthpala Kavindi Rupasinghe Koggala Marakkalage2, Tabish Arif3
1University of Agriculture Faisalabad, Faisalabad, 38000, Pakistan.
Abstract:
The mcr gene family, responsible for plasmid-mediated resistance to colistin, poses a growing threat to public health by reducing the efficacy of colistin, a critical last-resort antibiotic for multidrug-resistant Gram-negative bacteria. The mcr-1 gene, discovered in 2015, marked a significant shift in understanding colistin resistance, and subsequent mcr variants (mcr-2 to mcr-10) have emerged globally. These genes alter lipid A in bacterial cell membranes, decreasing colistin's binding and efficacy. The mcr genes are typically located on mobile plasmids, facilitating horizontal gene transfer across bacterial species. Our review examines the evolution, genetic mechanisms, and structural characteristics of the mcr gene family, discussing their spread across human, animal, and environmental contexts. In this review, we highlight the clinical implications of mcr-mediated resistance, noting the co-occurrence of mcr with other antimicrobial resistance determinants, which complicates treatment options. Additionally, it explores detection methods, global epidemiology, and potential strategies to combat mcr resistance, including the development of inhibitors and CRISPR-based gene editing. Our review concludes that combating mcr-mediated colistin resistance requires global surveillance, coordination across sectors, and continued research to stop its spread and impact.
Insights
The mcr gene family causes plasmid-mediated colistin resistance, threatening public health by reducing antibiotic effectiveness. Combating this requires global surveillance and research to control the spread of these resistance genes.
Area of Science:
- Microbiology
- Genetics
- Public Health
Background:
- The mcr gene family confers plasmid-mediated colistin resistance, a critical threat to treating multidrug-resistant Gram-negative bacteria.
- Colistin is a last-resort antibiotic, and its efficacy is compromised by mcr genes, which have rapidly emerged globally since 2015.
- These genes modify bacterial lipid A, hindering colistin binding and leading to resistance.
Purpose of the Study:
- To review the evolution, genetic mechanisms, and structural characteristics of the mcr gene family.
- To discuss the global spread of mcr genes in human, animal, and environmental settings.
- To highlight clinical implications, epidemiology, detection, and control strategies for mcr-mediated resistance.
Main Methods:
- Literature review of scientific publications on the mcr gene family.
- Analysis of genetic mechanisms, structural characteristics, and evolutionary pathways.
- Synthesis of epidemiological data and detection methods.
Main Results:
- The mcr gene family, including variants mcr-1 to mcr-10, confers colistin resistance through lipid A modification.
- Mcr genes are plasmid-located, facilitating horizontal gene transfer across diverse bacterial species and environments.
- Co-occurrence of mcr with other resistance genes complicates treatment strategies.
Conclusions:
- Combating mcr-mediated colistin resistance necessitates enhanced global surveillance and inter-sectoral collaboration.
- Continued research into novel detection methods, inhibitors, and gene-editing technologies is crucial.
- A coordinated global effort is essential to mitigate the spread and impact of mcr resistance.
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