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Bacteriophages and Their Host Range in Multidrug-Resistant Bacterial Disease Treatment
Ka Mun Chung1, Xiew Leng Liau1, Swee Seong Tang1,2
1Division of Microbiology and Molecular Genetics, Institute of Biological Sciences, Faculty of Sciences, University Malaya, Kuala Lumpur 50603, Malaysia.
Abstract:
The rapid emergence of multidrug-resistant (MDR) bacteria in recent times has prompted the search for new and more potent antibiotics. Bacteriophages (commonly known as phages) are viruses that target and infect their bacterial hosts. As such, they are also a potential alternative to antibiotics. These phages can be broadly categorized into monovalent (with a narrow host range spectrum and specific to a single bacterial genus) and polyvalent (with a broad host range and specific to more than two genera). However, there is still much ambiguity in the use of these terms, with researchers often describing their phages differently. There is considerable research on the use of both narrow- and broad-host range phages in the treatment of infections and diseases caused by MDR bacteria, including tuberculosis, cystic fibrosis, and carbapenem-resistant Enterobacterales (CRE) infectious diseases. From this, it is clear that the host range of these phages plays a vital role in determining the effectiveness of any phage therapy, and this factor is usually analyzed based on the advantages and limitations of different host ranges. There have also been efforts to expand phage host ranges via phage cocktail development, phage engineering and combination therapies, in line with current technological advancements. This literature review aims to provide a more in-depth understanding of the role of phage host ranges in the effectiveness of treating MDR-bacterial diseases, by exploring the following: phage biology, the importance of phages in MDR bacteria diseases treatment, the importance of phage host range and its advantages and limitations, current findings and recent developments, and finally, possible future directions for wide host range phages.
Insights
Bacteriophages (phages) offer a promising alternative to antibiotics for treating multidrug-resistant bacterial infections. Their effectiveness in phage therapy is significantly influenced by their host range, necessitating further research into optimizing this crucial characteristic.
Area of Science:
- Microbiology and Virology
- Infectious Diseases
- Antimicrobial Resistance
Background:
- The rise of multidrug-resistant (MDR) bacteria necessitates novel therapeutic strategies beyond traditional antibiotics.
- Bacteriophages (phages), viruses that infect bacteria, are emerging as a potential alternative to antibiotics.
- Phages are classified by host range: monovalent (narrow) and polyvalent (broad), though terminology lacks standardization.
Purpose of the Study:
- To elucidate the critical role of phage host range in the efficacy of phage therapy against MDR bacterial diseases.
- To explore the advantages and limitations associated with narrow- and broad-host range phages.
- To review current advancements and future directions in optimizing phage host ranges for therapeutic applications.
Main Methods:
- Literature review synthesizing existing research on phage biology and host range.
- Analysis of studies investigating narrow- and broad-host range phages in treating MDR bacterial infections.
- Examination of strategies for expanding phage host ranges, including phage cocktails and engineering.
Main Results:
- Phage host range is a key determinant of therapeutic effectiveness against MDR bacteria.
- Both narrow- and broad-host range phages have demonstrated utility in treating infections like tuberculosis, cystic fibrosis, and CRE.
- Ongoing research focuses on enhancing phage efficacy through cocktails, engineering, and combination therapies.
Conclusions:
- Understanding and optimizing phage host range is crucial for successful phage therapy.
- Further research into phage biology and host-range modulation is essential for combating MDR bacterial threats.
- Future directions involve developing strategies for wider host range phages and advanced therapeutic approaches.
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