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.

PubMed

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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