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Analysis of Four New Enterococcus faecalis Phages and Modeling of a Hyaluronidase Catalytic Domain from Saphexavirus.
Di Lallo, Gustavo; Falconi, Mattia; Iacovelli, Federico; Frezza, Domenico; D'Addabbo, Pietro.
Afiliación
  • Di Lallo G; Laboratory of Microbiology, Department of Biology, University of Roma Tor Vergata, Roma, Italy.
  • Falconi M; Structural Bioinformatics Group, Department of Biology, University of Roma Tor Vergata, Roma, Italy.
  • Iacovelli F; Structural Bioinformatics Group, Department of Biology, University of Roma Tor Vergata, Roma, Italy.
  • Frezza D; Laboratory of Microbiology, Department of Biology, University of Roma Tor Vergata, Roma, Italy.
  • D'Addabbo P; Computational Biology Unit, Department of Biology, University of Bari, Bari, Italy.
Phage (New Rochelle) ; 2(3): 131-141, 2021 Sep 01.
Article en En | MEDLINE | ID: mdl-36161247
ABSTRACT

Background:

Phage therapy (PT), as a method to treat bacterial infections, needs identification of bacteriophages targeting specific pathogenic host. Enterococcus faecalis, a Gram-positive coccus resident in the human gastrointestinal tract, may become pathogenic in hospitalized patients showing acquired resistance to vancomycin and thus representing a possible target for PT. Materials and

Methods:

We isolated four phages that infect E. faecalis and characterized them by host range screening, transmission electron microscopy, and genome sequencing. We also identified and three-dimensional modeled a new hyaluronidase enzyme.

Results:

The four phages belong to Siphoviridae family three Efquatrovirus (namely vB_EfaS_TV51, vB_EfaS_TV54, and vB_EfaS_TV217) and one Saphexavirus (vB_EfaS_TV16). All of them are compatible with lytic cycle. vB_EfaS_TV16 moreover presents a gene encoding for a hyaluronidase enzyme.

Conclusions:

The identified phages show features suggesting their useful application in PT, particularly the Saphexavirus that may be of enhanced relevance in PT because of its potential biofilm-digestion capability.
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