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Updated: Feb 16, 2026

Testing the Role of Multicopy Plasmids in the Evolution of Antibiotic Resistance
Published on: May 2, 2018
Expression characteristics of the plasmid-borne mcr-1 colistin resistance gene
Haifang Zhang1, Minhui Miao1, Jieting Yan1
1Department of Clinical Laboratory, The Second Affiliated Hospital of Soochow University, Suzhou, Jiangsu 215004, China.
Abstract:
The plasmid-encoded colistin resistance gene (mcr-1) has recently been reported in various Gram-negative species. However, the expression profile of mcr-1 remains unknown. Here, we investigated the expression of mcr-1 in various plasmids and bacteria. The mcr-1 expression levels in pMCR1_IncX4 varied from 1.81 × 10-5 to 1.05 × 10-4 (pmol per μg total RNA) in the two K. pneumoniae strains SZ03 and SZ04 (ST25) and the two E. coli strains SZ01 and CDA6 (ST2448 and ST167, respectively). The mcr-1 expression levels of pMCR1_IncI2 in E. coli SZ02 (ST2085) and E. coli BJ13 (ST457) were 5.27 × 10-5 and 2.58 × 10-5, respectively. In addition, the expression of chromosomal mcr-1 in ST156 E. coli BJ10 was 5.49×10-5. Interestingly, after 4μg/ml colistin treatment, mcr-1 in pMCR1_IncX4 increased 2- and 4-fold at 20 and 120 mins, respectively, in all pMCR1_IncX4-harboring strains, except for ST2448 E. coli, which had a lower expression after 20 mins that restored to baseline levels after 120 mins. In contrast, mcr-1 expression of pMCR1_IncI2 in the two E. coli strains (SZ02, BJ13) and the chromosomal mcr-1 in E. coli (BJ10) remained at baseline levels after 20 and 120 mins. In the same genetic background host strain E. coli E600, mcr-1 expression of pMCR1_IncX4 and pMCR1_IncI2 were similar and were decreased after colistin treatment for 20 min. However, mcr-1 in pMCR1_IncX4 was up-regulated after colistin treatment for 120 min, while mcr-1 in pMCR1_IncI2 was down-regulated compared to the untreated control. Our results suggested that mcr-1 has distinct expression profiles on different plasmids, bacterial hosts, and after antibiotic treatment.
Insights
The expression of the colistin resistance gene (mcr-1) varies significantly across different plasmids and bacterial hosts. Colistin treatment differentially affects mcr-1 expression, highlighting distinct regulatory mechanisms.
Area of Science:
- Microbiology
- Genetics
- Molecular Biology
Background:
- The plasmid-encoded colistin resistance gene, mcr-1, is increasingly detected in Gram-negative bacteria.
- Understanding the expression profile of mcr-1 is crucial for monitoring its spread and impact.
Purpose of the Study:
- To investigate the expression levels of the mcr-1 gene in various bacterial hosts and plasmids.
- To analyze the impact of colistin treatment on mcr-1 gene expression.
Main Methods:
- Quantification of mcr-1 expression levels (pmol per μg total RNA) in different strains of Klebsiella pneumoniae and Escherichia coli harboring various plasmids.
- Analysis of mcr-1 expression in response to colistin treatment over time (20 and 120 minutes).
- Comparison of mcr-1 expression from different plasmids (pMCR1_IncX4, pMCR1_IncI2) and chromosomal location.
Main Results:
- mcr-1 expression levels varied between different plasmids (pMCR1_IncX4, pMCR1_IncI2) and bacterial hosts, including K. pneumoniae and E. coli.
- Colistin treatment induced a significant increase in mcr-1 expression from pMCR1_IncX4 in most strains, with notable exceptions.
- mcr-1 expression from pMCR1_IncI2 and chromosomal mcr-1 showed minimal changes after colistin treatment, suggesting differential regulation.
Conclusions:
- The expression profile of mcr-1 is highly dependent on the plasmid type, bacterial host, and antibiotic exposure.
- Distinct regulatory mechanisms govern mcr-1 expression on different plasmids and under antibiotic pressure.
- These findings provide critical insights into the dynamics of colistin resistance gene expression.
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