The insect antimicrobial peptide cecropin A disrupts uropathogenic Escherichia coli biofilms

NPJ Biofilms Microbiomes. 2020 Feb 12;6(1):6. doi: 10.1038/s41522-020-0116-3.

Abstract

Current antibiotics cannot eradicate uropathogenic Escherichia coli (UPEC) biofilms, leading to recurrent urinary tract infections. Here, we show that the insect antimicrobial peptide cecropin A (CecA) can destroy planktonic and sessile biofilm-forming UPEC cells, either alone or when combined with the antibiotic nalidixic acid (NAL), synergistically clearing infection in vivo without off-target cytotoxicity. The multi-target mechanism of action involves outer membrane permeabilization followed by biofilm disruption triggered by the inhibition of efflux pump activity and interactions with extracellular and intracellular nucleic acids. These diverse targets ensure that resistance to the CecA + NAL combination emerges slowly. The antimicrobial mechanisms of CecA, thus, extend beyond pore-forming activity to include an unanticipated biofilm-eradication process, offering an alternative approach to combat antibiotic-resistant UPEC infections.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antimicrobial Cationic Peptides / administration & dosage*
  • Antimicrobial Cationic Peptides / pharmacology
  • Biofilms / drug effects*
  • Cell Membrane Permeability / drug effects
  • Disease Models, Animal
  • Drug Synergism
  • Escherichia coli Infections / microbiology*
  • Escherichia coli Infections / mortality
  • Escherichia coli Proteins / genetics
  • Gene Expression Regulation, Bacterial / drug effects
  • Lepidoptera
  • Microbial Sensitivity Tests
  • Microbial Viability / drug effects
  • Mortality
  • Nalidixic Acid / pharmacology*
  • Pore Forming Cytotoxic Proteins / administration & dosage*
  • Pore Forming Cytotoxic Proteins / pharmacology
  • Uropathogenic Escherichia coli / drug effects
  • Uropathogenic Escherichia coli / genetics
  • Uropathogenic Escherichia coli / growth & development*

Substances

  • Antimicrobial Cationic Peptides
  • Escherichia coli Proteins
  • Pore Forming Cytotoxic Proteins
  • Nalidixic Acid
  • cecropin A