清脆的
质粒
抗生素耐药性
生物
计算生物学
基因组编辑
机制(生物学)
生物技术
微生物学
抗生素
基因
遗传学
认识论
哲学
作者
Chenyu Wang,Zhi-Zhi Liu,Biao Tang,Hua Yang,Dongchang Sun
出处
期刊:PubMed
[National Institutes of Health]
日期:2022-04-25
卷期号:38 (4): 1432-1445
被引量:1
标识
DOI:10.13345/j.cjb.210348
摘要
Bacterial multi-drug resistance (MDR) is a global challenge in the fields of medicine and health, agriculture and fishery, ecology and environment. The cross-region spread of antibiotic resistance genes (ARGs) among different species is one of the main cause of bacterial MDR. However, there is no effective strategies for addressing the intensifying bacterial MDR. The CRISPR-Cas system, consisting of clustered regularly interspaced short palindromic repeats (CRISPR) and CRISPR associated proteins, can targetedly degrade exogenous nucleic acids, thus exhibiting high application potential in preventing and controlling bacterial MDR caused by ARGs. This review briefly introduced the working mechanism of CRISPR-Cas systems, followed by discussing recent advances in reducing ARGs by CRISPR-Cas systems delivered through mediators (e.g. plasmids, bacteriophages and nanoparticle). Moreover, the trends of this research field were envisioned, providing a new perspective on preventing and controlling MDR.
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