4.7 Article

Emerging pollutant metformin in water promotes the development of multiple-antibiotic resistance in Escherichia coli via chromosome mutagenesis

Journal

JOURNAL OF HAZARDOUS MATERIALS
Volume 430, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.jhazmat.2022.128474

Keywords

Metformin; Multiple antibiotic resistance; Efflux system; Chromosome mutagenesis

Funding

  1. National Natural Science Foundation of China [82103798, 81972994]
  2. Natural Science Foundation of Tianjin, China [19JCZDJC39900]

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This study investigates the role of the emerging pollutant metformin in facilitating antibiotic resistance. The results show that metformin can induce multiple-antibiotic resistance in Escherichia coli through increased efflux systems and decreased protein complexes. The findings suggest that metformin may contribute to the spread of antibiotic resistance in bacterial populations.
Antibiotics are known to be key drivers of antibiotic resistance and antibiotic resistance gene transmission. However, the contribution of the emerging pollutant metformin in facilitating antibiotic resistance remains unclear. In this study, Escherichia coli K12 (E. coli) was exposed to metformin at concentrations ranging from 10-7 to 200 mg/L, and antibiotic susceptibility test of isolated mutants was evaluated. DNA and RNA sequencing and real-time quantitative PCR (qPCR) were performed to identify the underlying mechanisms. The results showed metformin concentrations ranging from 10(-6) to 200 mg/L caused multiple-antibiotic resistance in E. coli. After 1 day exposure to metformin at 1 ng/L, the mutation frequency in E. coli increased to 1.24 x 10(-8), and it further increased to 7.13 x 10(-8) when prolonged to 5 days. And the mutants showed multiple-antibiotic resistance. Whole-genome DNA analysis of mutants showed chromosome mutagenesis in marR, tonB, and fhuA. Global transcriptional analysis and qPCR revealed the expressions of emrK, emrY, cusB, cusC, hycA, cecR, marA, acrA, and acrB were upregulated and those of tonB and fhuA were significantly downregulated. Thus, an increase in efflux systems AcrAB-TolC, EmrKY-TolC, and CusCFBA together with a decrease in FhuA-TonB protein complex play vital roles in the multiple-antibiotic resistance induced by metformin.

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