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.

Oncotarget
|January 4, 2018
PubMed

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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