Potential for bacteriophage therapy for Staphylococcus aureus pneumonia with influenza A coinfection
Peter G Speck1, Morgyn S Warner2,3,4, Shailesh Bihari5,6
1Flinders University of South Australia, College of Science and Engineering, Bedford Park, SA, 5042, Australia.
Abstract:
The ability of influenza A virus to evolve, coupled with increasing antimicrobial resistance, could trigger an influenza pandemic with great morbidity and mortality. Much of the 1918 influenza pandemic mortality was likely due to bacterial coinfection, including Staphylococcus aureus pneumonia. S. aureus resists many antibiotics. The lack of new antibiotics suggests alternative antimicrobials, such as bacteriophages, are needed. Potential delivery routes for bacteriophage therapy (BT) include inhalation and intravenous injection. BT has recently been used successfully in compassionate access pulmonary infection cases. Phage lysins, enzymes that hydrolyze bacterial cell walls and which are bactericidal, are efficacious in animal pneumonia models. Clinical trials will be needed to determine whether BT can ameliorate disease in influenza and S. aureus coinfection.
Insights
Antimicrobial resistance and evolving influenza A pose pandemic risks. Bacteriophage therapy offers a promising alternative to antibiotics for treating bacterial coinfections like Staphylococcus aureus pneumonia.
Area of Science:
- Virology
- Microbiology
- Infectious Diseases
- Antimicrobial Resistance
Background:
- Influenza A virus evolution and rising antimicrobial resistance threaten pandemic preparedness.
- Bacterial coinfections, such as Staphylococcus aureus pneumonia, significantly contributed to mortality during the 1918 influenza pandemic.
- Staphylococcus aureus exhibits resistance to numerous antibiotics, necessitating novel therapeutic strategies.
Purpose of the Study:
- To explore bacteriophage therapy (BT) as an alternative antimicrobial approach for influenza and Staphylococcus aureus coinfections.
- To review potential delivery routes and recent successes of BT in pulmonary infections.
- To assess the efficacy of phage lysins in preclinical models for bacterial pneumonia.
Main Methods:
- Literature review of bacteriophage therapy applications.
- Analysis of bacteriophage delivery routes (inhalation, intravenous injection).
- Examination of phage lysin efficacy in animal pneumonia models.
Main Results:
- Bacteriophage therapy has shown recent success in compassionate use cases for pulmonary infections.
- Phage lysins are bactericidal and effective in animal models of pneumonia.
- The study highlights the need for clinical trials to validate BT for influenza and S. aureus coinfection.
Conclusions:
- Bacteriophage therapy presents a viable alternative to conventional antibiotics against drug-resistant bacteria.
- Further clinical investigation is crucial to establish the therapeutic potential of BT in managing severe respiratory coinfections.
- Addressing coinfections is critical for mitigating morbidity and mortality in future influenza pandemics.
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