Bacteriophages and phage-delivered CRISPR-Cas system as antibacterial therapy.

Int J Antimicrob Agents

Departments of Laboratory Medicine and Internal Medicine, National Taiwan University Hospital, National Taiwan University College of Medicine, National Taiwan University, Taipei, Taiwan; Departments of Laboratory Medicine and Internal Medicine, China Medical University Hospital, Taichung, Taiwan; School of Medicine, China Medical University, Taichung, Taiwan; PhD Programme for Aging, School of Medicine, China Medical University, Taichung, Taiwan. Electronic address:

Published: January 2022

AI Article Synopsis

  • Multidrug-resistant bacterial infections are increasingly threatening human health globally due to the rise of antimicrobial resistance.
  • Phage therapy is emerging as a promising solution to fight these MDR bacteria, with numerous successful applications documented.
  • The review highlights randomized control trials of phage therapy and illustrates how the CRISPR-Cas system can be effectively delivered via phage vectors to create new antimicrobials.

Article Abstract

Multidrug-resistant (MDR) bacterial infections in humans are increasing worldwide. The global spread of antimicrobial resistance poses a considerable threat to human health. Phage therapy is a promising approach to combat MDR bacteria. An increasing number of reports have been published on phage therapy and the successful application of antibacterials derived using this method. Additionally, the CRISPR-Cas system has been used to develop antimicrobials with bactericidal effects in vivo. The CRISPR-Cas system can be delivered into target bacteria in various ways, with phage-based vectors being reported as an effective method. In this review, we briefly summarise the results of randomised control trials on bacteriophage therapy. Moreover, we integrated mechanisms of the CRISPR-Cas system antimicrobials in a schematic diagram and consolidated the research on phage-delivered CRISPR-Cas system antimicrobials.

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Source
http://dx.doi.org/10.1016/j.ijantimicag.2021.106475DOI Listing

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