Selection of a Gentamicin-Resistant Variant Following Polyhexamethylene Biguanide (PHMB) Exposure in Escherichia coli

Clémence Cuzin1, Paméla Houée1, Pierrick Lucas2

  • 1Antibiotics, Biocides, Residues and Resistance Unit, Fougères Laboratory, French Agency for Food, Environmental and Occupational Health & Safety (ANSES), 35300 Fougères, France.

Insights

The biocide polyhexamethylene biguanide (PHMB) can select for antibiotic resistance in Escherichia coli. A mutation in the aceE gene was identified as a mechanism for this cross-resistance to PHMB and gentamicin.

Area of Science:

  • Microbiology
  • Biochemistry
  • Molecular Biology

Background:

  • Antibiotic resistance is a major global health threat.
  • Biocides can potentially select for antibiotic resistance, but mechanisms are poorly understood.
  • Polyhexamethylene biguanide (PHMB) is a widely used biocide requiring investigation for resistance selection potential.

Purpose of the Study:

  • To investigate the potential of PHMB to select for antibiotic resistance in *Escherichia coli* biofilms.
  • To identify the mechanisms underlying PHMB-induced antibiotic resistance.

Main Methods:

  • Culturing *E. coli* biofilms on inox coupons.
  • Exposure of biofilms to sublethal PHMB concentrations over 10 days.
  • Isolation and characterization of antibiotic-resistant variants (phenotypic and genotypic analysis, whole-genome sequencing).

Main Results:

  • PHMB exposure selected for a stable gentamicin-resistant *E. coli* variant (Ec04m1) with an 8-fold increase in MIC.
  • The resistant variant exhibited a decreased growth rate.
  • Whole-genome sequencing revealed a nonsense mutation in the *aceE* gene (encoding pyruvate dehydrogenase E1 component) in Ec04m1.
  • The *aceE* mutation conferred decreased susceptibility to both PHMB and gentamicin, confirmed by growth experiments with acetate.

Conclusions:

  • Polyhexamethylene biguanide (PHMB) can select for antibiotic resistance in *E. coli* biofilms.
  • Mutations in central metabolic pathway enzymes, such as *aceE*, can lead to cross-resistance to biocides and antibiotics.
  • Metabolic enzymes represent potential targets for bacterial adaptation strategies leading to cross-resistance.