Efficacy and safety assessment of two enterococci phages in an in vitro biofilm wound model

Sci Rep. 2019 Apr 30;9(1):6643. doi: 10.1038/s41598-019-43115-8.

Abstract

Chronic wounds affect thousands of people worldwide, causing pain and discomfort to patients and represent significant economical burdens to health care systems. The treatment of chronic wounds is very difficult and complex, particularly when wounds are colonized by bacterial biofilms which are highly tolerant to antibiotics. Enterococcus faecium and Enterococcus faecalis are within the most frequent bacteria present in chronic wounds. Bacteriophages (phages) have been proposed as an efficient and alternative against antibiotic-resistant infections, as those found in chronic wounds. We have isolated and characterized two novel enterococci phages, the siphovirus vB_EfaS-Zip (Zip) and the podovirus vB_EfaP-Max (Max) to be applied during wound treatment. Both phages demonstrated lytic behavior against E. faecalis and E. faecium. Genome analysis of both phages suggests the absence of genes associated with lysogeny. A phage cocktail containing both phages was tested against biofilms formed in wound simulated conditions at a multiplicity of infection of 1.0 and a 2.5 log CFU.mL-1 reduction in the bacterial load after at 3 h of treatment was observed. Phages were also tested in epithelial cells colonized by these bacterial species and a 3 log CFU.mL-1 reduction was observed using both phages. The high efficacy of these new isolated phages against multi-species biofilms, their stability at different temperatures and pH ranges, short latent periods and non-cytotoxicity to epithelial cells suggest their therapeutic use to control infectious biofilms present in chronic wounds.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 3T3 Cells
  • Animals
  • Bacteriolysis
  • Bacteriophages / isolation & purification
  • Bacteriophages / physiology*
  • Bacteriophages / ultrastructure
  • Biofilms*
  • Cell Survival
  • Enterococcus / virology*
  • Epithelial Cells / virology
  • Genes, Viral
  • Host Specificity
  • Humans
  • Hydrogen-Ion Concentration
  • Mice
  • Phage Therapy*
  • Temperature
  • Wound Infection / microbiology*
  • Wound Infection / therapy*