4.7 Article

Anti-CRISPR proteins as a therapeutic agent against drug-resistant bacteria

Journal

MICROBIOLOGICAL RESEARCH
Volume 257, Issue -, Pages -

Publisher

ELSEVIER GMBH
DOI: 10.1016/j.micres.2022.126963

Keywords

Acrs; Bacteriophages; CRISPR-Cas system; Multidrug resistance; Phage therapy

Categories

Funding

  1. Rashtriya Uchchatar Shiksha Abhiyan (RUSA), a Centrally Sponsored Scheme (CSS), New Delhi [F30(16)/SPD/RUSA/2016/178]
  2. Department of Science and Technology, New Delhi (SERB) [EEQ/2020/000011]

Ask authors/readers for more resources

The continuous use of antibiotics has led to multidrug resistance among bacterial populations, posing a significant threat to public health. Anti-CRISPR proteins have been identified as potential therapeutic agents against drug-resistant bacteria.
The continuous deployment of various antibiotics to treat multiple serious bacterial infections leads to multidrug resistance among the bacterial population. It has failed the standard treatment strategies through different antibacterial agents and serves as a significant threat to public health worldwide at devastating levels. The discovery of anti-CRISPR proteins catches the interest of researchers around the world as a promising therapeutic agent against drug-resistant bacteria. Anti-CRISPR proteins are known to inhibit bacterial CRISPR-Cas defense systems in multiple possible ways. The CRISPR-Cas nucleoprotein assembly provides adaptive immunity in bacteria against diverse categories of phage infections. Parallelly, phages also try to break the CRISPR-Cas barrier by producing anti-CRISPR proteins, leading to growth inhibition and bacterial lysis. This review begins with a brief description of the bacterial CRISPR-Cas system, followed by a detailed portrayal of anti-CRISPR proteins, including their discovery and evolution, mechanism of action, regulation of expression, and potential applications in the healthcare sector as an alternative therapeutic strategy to combat severe bacterial infections.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available