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Updated: Jun 15, 2026

Biosensor for Detection of Antibiotic Resistant Staphylococcus Bacteria
Published on: May 8, 2013
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.
Abstract:
A novel bacteriophage, phiMR25, was isolated from a lysogenic Staphylococcus aureus strain by mitomycin C induction. Its biological features were analyzed in comparison with phiMR11, which was described previously as a prototype therapeutic phage. phiMR25 is morphologically similar to phiMR11 (morphotype B1 of family Myoviridae) but has a broader host range than phiMR11 on S. aureus strains. phiMR25 can also multiply on S. aureus lysogens of phiMR11. Its DNA is 44,342 bp in size, is predicted to include 70 open reading frames, and does not contain genes related to toxin or drug resistance. The lysogenic module and most of the putative virion protein genes are completely different from those of phiMR11. In spite of their genetic diversity, intraperitoneal administration of phiMR25 rescued mice inoculated with a lethal dose of S. aureus, as was the case for phiMR11. These results suggest that phiMR25 could be another candidate phage to treat S. aureus infection.
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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