Related Experiment Video
Updated: May 2, 2026

Alveolar Macrophage Phagocytosis and Bacteria Clearance in Mice
Published on: March 2, 2019
Experimental phage therapy against lethal lung-derived septicemia caused by Staphylococcus aureus in mice
Iyo Takemura-Uchiyama1, Jumpei Uchiyama2, Makoto Osanai3
1Department of Microbiology and Infection, Faculty of Medicine, Kochi University, Kochi, Japan; Clinical Laboratory, Kochi University Hospital, Kochi, Japan.
Abstract:
Nosocomial respiratory infections caused by methicillin-resistant Staphylococcus aureus (MRSA) can progress to lethal systemic infections. Bacteriophage (phage) therapy is expected to be effective against these critical infections. Previously, phage S13' was proposed as a potential therapeutic phage. We here examined phage treatment in a mouse model of lung-derived septicemia using phage S13'. Intraperitoneal phage administration at 6 h postinfection reduced the severity of infection and rescued the infected mice. Phage S13' can efficiently lyse hospital-acquired MRSA strains causing pneumonia-associated bacteremia in vitro. Thus, phage therapy may be a possible therapeutic intervention in staphylococcal lung-derived septicemia.
Insights
Bacteriophage (phage) therapy using S13
Area of Science:
- Microbiology
- Infectious Diseases
- Bacteriophage Therapy
Background:
- Nosocomial respiratory infections caused by methicillin-resistant Staphylococcus aureus (MRSA) pose a significant threat, potentially leading to fatal systemic infections.
- Bacteriophage therapy presents a promising alternative for combating critical infections, particularly those caused by antibiotic-resistant bacteria.
- Phage S13' has been previously identified as a potential candidate for therapeutic applications against MRSA.
Purpose of the Study:
- To evaluate the efficacy of phage S13' in a mouse model of lung-derived septicemia caused by MRSA.
- To assess the in vitro lytic activity of phage S13' against hospital-acquired MRSA strains.
Main Methods:
- A mouse model of MRSA-induced lung-derived septicemia was established.
- Intraperitoneal administration of phage S13' was performed at 6 hours post-infection.
- In vitro experiments were conducted to determine the lytic activity of phage S13' against clinical MRSA isolates.
Main Results:
- Intraperitoneal administration of phage S13' significantly reduced infection severity in the mouse model.
- Phage S13' treatment led to the rescue of infected mice, improving survival rates.
- In vitro assays demonstrated that phage S13' efficiently lyses hospital-acquired MRSA strains responsible for pneumonia-associated bacteremia.
Conclusions:
- Phage S13' therapy shows potential as a viable treatment option for staphylococcal lung-derived septicemia.
- Bacteriophage therapy offers a promising strategy to combat MRSA infections, especially in the context of rising antibiotic resistance.
- Further research into phage S13' could pave the way for novel therapeutic interventions against severe bacterial infections.
More Related Videos
07:43A Non-invasive and Technically Non-intensive Method for Induction and Phenotyping of Experimental Bacterial Pneumonia in Mice
Published on: September 28, 2016
13:45A Precise Pathogen Delivery and Recovery System for Murine Models of Secondary Bacterial Pneumonia
Published on: September 21, 2019