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CRISPR-Cas, a Revolution in the Treatment and Study of ESKAPE Infections: Pre-Clinical Studies

期刊

ANTIBIOTICS-BASEL
卷 10, 期 7, 页码 -

出版社

MDPI
DOI: 10.3390/antibiotics10070756

关键词

CRISPR-Cas; ESKAPE pathogens; treatment

资金

  1. National Plan for Scientific Research, Technological Development and Innovation [PI16/01163, PI19/00878]
  2. ISCIII-Deputy General Directorate for Evaluation and Promotion of Research-European Regional Development Fund A way of Making Europe and Instituto de Salud Carlos III FEDER, Spanish Network for the Research in Infectious Diseases (REIPI) [RD16/0016/0006]
  3. Study Group on Mechanisms of Action and Resistance to Antimicrobials, GEMARA (SEIMC)
  4. pFIS program (ISCIII) [FI20/00302]
  5. GAIN, Xunta de Galicia [IN606A-2020/035, IN606B-2018/008]
  6. Rio Hortega program (ISCIII) [CM20/00198]

向作者/读者索取更多资源

One of the biggest global threats is the emergence of antimicrobial-resistant bacteria, particularly the ESKAPE group pathogens with high drug resistance and virulence. Innovative treatment strategies are needed, including the use of CRISPR-Cas technologies for targeted mutations and functional gene loss.
One of the biggest threats we face globally is the emergence of antimicrobial-resistant (AMR) bacteria, which runs in parallel with the lack in the development of new antimicrobials. Among these AMR bacteria pathogens belonging to the ESKAPE group can be highlighted (Enterococcus spp., Staphylococcus aureus, Klebsiella pneumoniae, Acinetobacter baumannii, Pseudomonas aeruginosa and Enterobacter spp.) due to their profile of drug resistance and virulence. Therefore, innovative lines of treatment must be developed for these bacteria. In this review, we summarize the different strategies for the treatment and study of molecular mechanisms of AMR in the ESKAPE pathogens based on the clustered regularly interspaced short palindromic repeats (CRISPR) and CRISPR-associated (Cas) proteins' technologies: loss of plasmid or cellular viability, random mutation or gene deletion as well directed mutations that lead to a gene's loss of function.

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