Phage-Bacteria Interactions in Potential Applications of Bacteriophage vB_EfaS-271 against Enterococcus faecalis

Gracja Topka-Bielecka1, Bożena Nejman-Faleńczyk1, Sylwia Bloch2

  • 1Department of Molecular Biology, University of Gdansk, Wita Stwosza 59, 80-308 Gdansk, Poland.

Viruses
|March 6, 2021
PubMed

Insights

Phage therapy offers an alternative to antibiotics for treating infections caused by antibiotic-resistant bacteria like Enterococcus faecalis. Bacteriophage vB_EfaS-271 effectively reduces E. faecalis in cultures and biofilms with low mammalian cell toxicity, showing potential for therapeutic use.

Area of Science:

  • Microbiology
  • Virology
  • Biotechnology

Background:

  • Antibiotic resistance in pathogens like Enterococcus faecalis necessitates alternative treatments.
  • Bacteriophages (phages) are viruses that infect bacteria and are a promising alternative to antibiotics.
  • Understanding phage-host interactions is crucial for developing effective phage therapy.

Purpose of the Study:

  • To evaluate the efficacy of bacteriophage vB_EfaS-271 against Enterococcus faecalis.
  • To investigate phage-host interactions, including biofilm penetration, toxicity, and resistance development.
  • To assess the potential of vB_EfaS-271 as a therapeutic agent.

Main Methods:

  • Isolation and characterization of bacteriophage vB_EfaS-271.
  • Assessment of phage efficacy in liquid cultures and biofilms.
  • Evaluation of phage particle toxicity to mammalian cells.
  • Determination of phage-resistant bacterial strain formation at various multiplicities of infection (m.o.i.).

Main Results:

  • Bacteriophage vB_EfaS-271 significantly reduced viable E. faecalis cells in both liquid cultures and biofilms.
  • Purified phage particles exhibited no considerable toxicity to mammalian cells.
  • The efficiency of phage-resistant bacterial strain formation was dependent on the m.o.i., being higher at a virion-cell ratio of 10 compared to lower m.o.i. values.

Conclusions:

  • Bacteriophage vB_EfaS-271 demonstrates significant antibacterial activity against E. faecalis.
  • The phage shows a favorable safety profile with low mammalian cell toxicity.
  • vB_EfaS-271 is a potential candidate for further development in phage therapy against E. faecalis infections.

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