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Published on: August 19, 2021
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.
Abstract:
Phage therapy is one of main alternative option for antibiotic treatment of bacterial infections, particularly in the era of appearance of pathogenic strains revealing resistance to most or even all known antibiotics. Enterococcus faecalis is one of such pathogens causing serious human infections. In the light of high level of biodiversity of bacteriophages and specificity of phages to bacterial species or even strains, development of effective phage therapy depend, between others, on identification and characterization of a large collection of these viruses, including understanding of their interactions with host bacterial cells. Recently, isolation of molecular characterization of bacteriophage vB_EfaS-271, infecting E. faecalis strains have been reported. In this report, phage-host interactions are reported, including ability of vB_EfaS-271 to infect bacteria forming biofilms, efficiency of eliminating bacterial cells from cultures depending on multiplicity of infection (m.o.i.), toxicity of purified phage particles to mammalian cells, and efficiency of appearance of phage-resistant bacteria. The presented results indicate that vB_EfaS-271 can significantly decrease number of viable E. faecalis cells in biofilms and in liquid cultures and reveals no considerable toxicity to mammalian cells. Efficiency of formation of phage-resistant bacteria was dependent on m.o.i. and was higher when the virion-cell ratio was as high as 10 than at low (between 0.01 and 0.0001) m.o.i. values. We conclude that vB_EfaS-271 may be considered as a candidate for its further use in phage therapy.
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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