Biological characteristics and anti-biofilm activity of a lytic phage against vancomycin-resistant Enterococcus

Forough Goodarzi1, Masoumeh Hallajzadeh1, Mohammad Sholeh1

  • 1Department of Microbiology, School of Medicine, Iran University of Medical Sciences, Tehran, Iran.

Abstract

Insights

A novel bacteriophage, vB-EfmS-S2, effectively targets and disrupts vancomycin-resistant Enterococcus faecium biofilms. This phage shows promise as an alternative treatment for drug-resistant bacterial infections.

Area of Science:

  • Microbiology
  • Bacteriophage Therapy
  • Antimicrobial Resistance

Background:

  • Antibiotic resistance in enterococci, particularly vancomycin-resistant Enterococcus faecium (VREfm), poses a significant global health threat.
  • The inefficiency of current antibiotics necessitates the exploration of alternative therapeutic strategies to combat drug-resistant pathogens.
  • Bacteriophages represent a promising alternative due to their specificity and ability to target resistant bacteria.

Purpose of the Study:

  • To isolate and characterize a bacteriophage effective against vancomycin-resistant Enterococcus faecium.
  • To evaluate the biological properties and efficacy of the isolated bacteriophage (vB-EfmS-S2) against VREfm.
  • To assess the phage's impact on VREfm biofilm formation and structure.

Main Methods:

  • Isolation of bacteriophage vB-EfmS-S2 from hospital sewage.
  • Determination of biological properties including host range, optimal pH and temperature, stability in bile, and Mg2+ requirement.
  • Assessment of phage S2's lytic activity and its effect on VREfm biofilm disruption using electron microscopy.

Main Results:

  • Phage S2 demonstrated specific lysis against a broad range of clinical VREfm isolates.
  • Electron microscopy confirmed phage S2 belongs to the Siphoviridae family.
  • Optimal conditions for phage S2 activity included pH 5-11 and temperatures of 30-45°C (peak at 37°C), with a latent period of 14 min and burst size of 200 PFU/ml. It tolerated 1-2% bile and required Mg2+.
  • Phage S2 significantly inhibited and disrupted VREfm biofilms.

Conclusions:

  • Bacteriophage S2 exhibits potent lytic activity against vancomycin-resistant Enterococcus faecium.
  • Phage S2 effectively inhibits and disrupts VREfm biofilms.
  • Phage S2 holds significant potential as an alternative therapeutic agent for controlling VREfm infections, particularly those involving biofilms.

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