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Endolysins, Depolymerases, Holins, and VALs: Phage-Derived Proteins for Combating Antimicrobial Resistance
Zahra Nasiri Shoeibi1, Farzaneh Rafiee2, Sousan Akrami1
1Department of Microbiology, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran.
Bacteriophage-derived enzymes like holins and endolysins offer novel antibacterial strategies against multidrug-resistant bacteria. These proteins, including depolymerases and virion-associated lysins, show promise in combating resistant infections.
Area of Science:
- Microbiology
- Biotechnology
- Infectious Diseases
Background:
- The increasing prevalence of multidrug-resistant (MDR) bacteria necessitates novel therapeutic approaches.
- Bacteriophages encode various lytic enzymes with antibacterial potential.
Purpose of the Study:
- To review the molecular mechanisms, advantages, limitations, and therapeutic applications of bacteriophage-derived lytic proteins against MDR infections.
- To highlight the potential of engineered phage enzymes as alternative antibacterials.
Main Methods:
- Review of existing literature on bacteriophage-encoded lytic proteins.
- Analysis of the distinct mechanisms of action for holins, endolysins, polysaccharide depolymerases, and virion-associated lysins (VALs).
- Discussion of natural and engineered forms of these enzymes, including "artilysins" and "chimeolysins".
Main Results:
- Phage lytic proteins disrupt bacterial cells or protective barriers through diverse mechanisms.
- Endolysins lyse Gram-positive bacteria and can be engineered for Gram-negative efficacy.
- Depolymerases degrade bacterial polysaccharides, while VALs facilitate phage DNA entry.
Conclusions:
- Phage-derived enzymes demonstrate rapid, specific bacteriolysis with low resistance potential.
- Challenges in delivery, stability, and immunogenicity require further research for therapeutic application.
- These enzymes represent a promising avenue for combating MDR bacterial infections.
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