Characterization of the Bacteriophage vB_EfaS-271 Infecting Enterococcus faecalis.
Gracja Topka-BieleckaSylwia BlochBożena Nejman-FaleńczykMichał GrabskiAgata Jurczak-KurekMarcin GórniakAleksandra DydeckaAgnieszka NecelGrzegorz WegrzynAlicja WęgrzynPublished in: International journal of molecular sciences (2020)
A newly isolated bacteriophage infecting Enterococcus faecalis strains has been characterized, including determination of its molecular features. This phage, named vB_EfaS-271, has been classified as a Siphoviridae member, according to electron microscopy characterization of the virions, composed of a 50 nm-diameter head and a long, flexible, noncontractable tail (219 × 12.5 nm). Analysis of the whole dsDNA genome of this phage showed that it consists of 40,197 bp and functional modules containing genes coding for proteins that are involved in DNA replication (including DNA polymerase/primase), morphogenesis, packaging and cell lysis. Mass spectrometry analysis allowed us to identify several phage-encoded proteins. vB_EfaS-271 reveals a relatively narrow host range, as it is able to infect only a few E. faecalis strains. On the other hand, it is a virulent phage (unable to lysogenize host cells), effectively and quickly destroying cultures of sensitive host bacteria, with a latent period as short as 8 min and burst size of approximately 70 phages per cell at 37 °C. This phage was also able to destroy biofilms formed by E. faecalis. These results contribute to our understanding of the biodiversity of bacteriophages, confirming the high variability among these viruses and indicating specific genetic and functional features of vB_EfaS-271.
Keyphrases
- pseudomonas aeruginosa
- mass spectrometry
- escherichia coli
- genome wide
- electron microscopy
- photodynamic therapy
- cell therapy
- cystic fibrosis
- induced apoptosis
- single molecule
- cell death
- liquid chromatography
- high resolution
- gene expression
- bone marrow
- signaling pathway
- cell cycle arrest
- candida albicans
- capillary electrophoresis
- mesenchymal stem cells
- transcription factor
- nucleic acid
- high performance liquid chromatography
- genome wide identification