KIIT School of Biotechnology, KIIT University, Bhubaneswar 751024, Odisha, India.
Imperial College, London SW7 2AZ, United Kingdom.
Biomed Pharmacother. 2022 Jul;151:113122. doi: 10.1016/j.biopha.2022.113122. Epub 2022 May 17.
The Host-microbiome interactions that exist inside the gut microbiota operate in a synergistic and abnormal manner. Additionally, the normal homeostasis and functioning of gut microbiota are frequently disrupted by the intervention of Multi-Drug Resistant (MDR) pathogens. CRISPR-Cas (CRISPR-associated protein with clustered regularly interspersed short palindromic repeats) recognized as a prokaryotic immune system has emerged as an effective genome-editing tool to edit and delete specific microbial genes for the expulsion of bacteria through bactericidal action. In this review, we demonstrate many functioning CRISPR-Cas systems against the anti-microbial resistance of multiple pathogens, which infiltrate the gastrointestinal tract. Moreover, we discuss the advancement in the development of a phage-delivered CRISPR-Cas system for killing a gut MDR pathogen. We also discuss a combinatorial approach to use bacteriophage as a delivery system for the CRISPR-Cas gene for targeting a pathogenic community in the gut microbiome to resensitize the drug sensitivity. Finally, we discuss engineered phage as a plausible potential option for the CRISPR-Cas system for pathogenic killing and improvement of the efficacy of the system.
肠道微生物群中的宿主-微生物相互作用以协同和异常的方式运作。此外,肠道微生物群的正常动态平衡和功能经常被多药耐药(MDR)病原体的干预所破坏。CRISPR-Cas(具有成簇规律间隔短回文重复的 CRISPR 相关蛋白)被认为是一种原核免疫系统,已成为一种有效的基因组编辑工具,可通过杀菌作用编辑和删除特定的微生物基因以驱逐细菌。在这篇综述中,我们展示了许多针对多种侵袭胃肠道的抗微生物耐药性的功能性 CRISPR-Cas 系统。此外,我们讨论了开发噬菌体递送 CRISPR-Cas 系统以杀死肠道 MDR 病原体的进展。我们还讨论了一种组合方法,即使用噬菌体作为 CRISPR-Cas 基因的递送系统,以针对肠道微生物组中的致病群落,重新敏感药物敏感性。最后,我们讨论了工程噬菌体作为 CRISPR-Cas 系统用于病原杀伤和提高系统功效的合理潜在选择。