Isolation and characterization of a novel Staphylococcus aureus bacteriophage, phiMR25, and its therapeutic potential

Hiroshi Hoshiba1, Jumpei Uchiyama, Shin-ichiro Kato

  • 1Department of Pediatrics, Kochi Medical School, Nankoku, Kochi 783-8505, Japan.

Archives of Virology
|March 13, 2010
PubMed

Insights

A new bacteriophage, phiMR25, effectively treats Staphylococcus aureus infections in mice. This phage shows promise as a therapeutic agent due to its broad host range and safety profile.

Area of Science:

  • Microbiology
  • Virology
  • Bacteriophage Therapy

Background:

  • Staphylococcus aureus is a significant human pathogen.
  • Bacteriophage therapy is an emerging alternative to antibiotics.
  • phiMR11 is a previously identified therapeutic phage for S. aureus.

Purpose of the Study:

  • To isolate and characterize a novel bacteriophage, phiMR25, from a lysogenic S. aureus strain.
  • To compare the biological and genetic features of phiMR25 with the prototype therapeutic phage phiMR11.
  • To evaluate the therapeutic potential of phiMR25 against S. aureus infection in a mouse model.

Main Methods:

  • Isolation of bacteriophage phiMR25 via mitomycin C induction.
  • Morphological analysis and host range determination on S. aureus strains.
  • Genomic sequencing and analysis of open reading frames.
  • In vivo efficacy study using a lethal dose of S. aureus in mice.

Main Results:

  • phiMR25, a Myoviridae bacteriophage, exhibits a broader host range than phiMR11 against S. aureus.
  • phiMR25's genome is 44,342 bp with 70 predicted open reading frames, lacking toxin or resistance genes.
  • phiMR25 shares genetic diversity with phiMR11, particularly in lysogenic and virion protein genes.
  • Intraperitoneal administration of phiMR25 successfully rescued mice from lethal S. aureus infection.

Conclusions:

  • phiMR25 is a novel bacteriophage with significant therapeutic potential against S. aureus infections.
  • Its broader host range and demonstrated in vivo efficacy make it a strong candidate for phage therapy.
  • phiMR25 represents a valuable alternative or adjunct to conventional antibiotic treatments for S. aureus.

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