CRISPR-Cas9系统:对抗耐药性的革命性工具:撤回

IF 2 Q3 INFECTIOUS DISEASES
Osmond C Ekwebelem, Job C. Aleke, Ekenedirichukwu S. Ofielu, Obinna V. Nnorom-Dike
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引用次数: 5

摘要

快速发展的抗菌素耐药性世界不仅使对抗传染病变得困难,而且在过去的几十年里,也使新型抗菌素的发现陷入停滞。近年来,研究人员发现了聚集规律间隔短回文重复序列(CRISPR)相关(CRISPR- cas)系统作为替代治疗的潜力。自从CRISPR-Cas9作为细菌的“适应性免疫系统”被发现以来,CRISPR-Cas9系统已被改进为最先进的基因工程工具,具有在几乎所有微生物中引起特定基因插入和/或基因缺失的令人印象深刻的能力。新出现的图像表明,CRISPR-Cas9系统可以以序列特异性的方式被利用,以选择性地消除混合微生物群体中的单个细菌菌株,和/或使细菌对抗生素重新敏感。这些发现不仅使生物医学研究发生了革命性的变化,而且可能在为耐多药感染创造新的替代疗法方面发挥关键作用。在这里,我们讨论了这一领域的最新发现,以及利用CRISPR-Cas9作为对抗抗菌素耐药性的新技术所涉及的方法。我们还强调了最近在靶向致病性和耐药细菌的背景下利用CRISPR-Cas9系统的研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
CRISPR-Cas9 System: A Revolutionary Tool in the Fight Against Antimicrobial Resistance: Retracted
Abstract The rapidly evolving world of antimicrobial resistance has not only made it difficult to combat infectious diseases, but during the last decades also brought the discovery of novel antimicrobials to a standstill. In recent years, researchers discovered the potential of the clustered regularly interspaced short palindromic repeats (CRISPR)-associated (CRISPR-Cas) system as an alternative therapeutic. Since the unearthing of CRISPR-Cas9 as an “adaptive immune system” of bacteria, the CRISPR-Cas9 system has been improved into a state-of-the-art genetic engineering tool, with an impressive ability to cause specific gene insertions and/or gene deletions, in almost all microorganisms. The emerging picture suggests that the CRISPR-Cas9 system can be exploited in a sequence-specific manner to selectively eliminate individual bacterial strains in a mixed microbial population, and/or re-sensitize bacteria to antibiotics. These findings have not only revolutionized biomedical research, but might also prove to be pivotal in creating novel alternative treatments for multidrug-resistant infections. Here, we discussed the up-to-date findings reported in this area, as well as the approaches involved in the utilization of CRISPR-Cas9 as a novel technology in the fight against antimicrobial resistance. We also highlighted recent studies that have exploited the CRISPR-Cas9 system in the context of targeting pathogenic and drug-resistant bacteria.
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