Biological characteristics and genome analysis of Enterococcus faecalis phage vB_EfS_L1
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Published on: December 23, 2022
Huijun Geng1, Yong Chang2, Yanqiu Zhou2
1Anshan Normal University, Anshan, 114000, People's Republic of China. genghuijun@asnc.edu.cn.
Abstract:
This study focuses on the isolation, identification, and characterization of Enterococcus faecalis strain Ef-01 and the bacteriophage vB_EfS_L1 targeting it. E. faecalis was isolated from hospital laboratory samples and confirmed through PCR analysis, yielding a 1466 bp sequence with high homology to E. faecalis ATCC 19433. Antibiotic sensitivity testing revealed that Ef-01 was susceptible to six antibiotics including ciprofloxacin and linezolid, intermediately susceptible to four, and resistant to five antibiotics such as penicillin and cefradine. Subsequently, bacteriophage vB_EfS_L1 was isolated from hospital wastewater and purified through multiple rounds of plaque purification. The highest titer, reaching 4.0 × 1011 PFU/mL, was achieved when propagation was carried out at a multiplicity of infection (MOI) of 0.01. Host range analysis revealed that phage vB_EfS_L1 lysed 40% of clinical Enterococcus isolates, including multidrug-resistant strains, demonstrating a moderate yet clinically relevant tropism. Further analysis showed that vB_EfS_L1 exhibited excellent stability at temperatures from -20 to 37 °C, but was inactivated at 80 °C. It also maintained activity across a pH range of 4-10, with the highest activity at acidic pH values. The bacteriophage displayed resistance to chloroform and ether but was sensitive to SDS and proteinase K. Additionally, the bacteriophage was UV-sensitive, with a rapid decline in titer upon prolonged exposure. The genome of vB_EfS_L1, consisting of 41.151 bp, was analyzed, revealing genes related to structural components, DNA replication, host lysis, and packaging. Functional gene predictions confirmed the absence of lysogeny or virulence-associated genes, ensuring the safety of vB_EfS_L1 for potential therapeutic applications. These findings highlight the bacteriophage's potential as a therapeutic agent against E. faecalis, contributing to the development of phage-based interventions in bacterial infections.
Insights
This study isolated and characterized Enterococcus faecalis Ef-01 and its targeting bacteriophage vB_EfS_L1. The bacteriophage shows potential as a safe therapeutic agent against multidrug-resistant Enterococcus faecalis infections.
Area of Science:
- Microbiology
- Molecular Biology
- Biotechnology
Background:
- Enterococcus faecalis is a significant cause of hospital-acquired infections.
- Antibiotic resistance in E. faecalis necessitates alternative treatment strategies.
- Bacteriophage therapy offers a promising alternative to antibiotics.
Purpose of the Study:
- To isolate and characterize a specific strain of Enterococcus faecalis (Ef-01).
- To isolate and characterize a bacteriophage (vB_EfS_L1) targeting E. faecalis Ef-01.
- To evaluate the therapeutic potential of bacteriophage vB_EfS_L1 against E. faecalis.
Main Methods:
- Isolation and identification of E. faecalis using PCR.
- Antibiotic sensitivity testing of E. faecalis Ef-01.
- Isolation, purification, and titer determination of bacteriophage vB_EfS_L1.
- Host range analysis, stability testing (temperature, pH), and genome sequencing of the bacteriophage.
Main Results:
- E. faecalis Ef-01 confirmed with high homology to ATCC 19433, exhibiting multidrug resistance.
- Bacteriophage vB_EfS_L1 isolated with a high titer (4.0 × 10^11 PFU/mL).
- Phage vB_EfS_L1 lysed 40% of clinical Enterococcus isolates, including multidrug-resistant strains, and demonstrated stability under various conditions. Its genome lacks lysogeny and virulence genes.
Conclusions:
- Bacteriophage vB_EfS_L1 is a promising candidate for therapeutic applications against E. faecalis.
- The characterized phage is stable and safe for potential use in combating bacterial infections.
- This research contributes to the development of phage-based interventions for multidrug-resistant bacteria.
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