清脆的
生物
微生物群
质粒
基因组编辑
计算生物学
Cas9
抗生素耐药性
大肠杆菌
微生物学
细菌
遗传学
抗生素
基因
DNA
作者
Kevin Neil,Nancy Allard,Patricia Roy,Frédéric Grenier,Alfredo Menéndez,Vincent Burrus,Sébastien Rodrigue
标识
DOI:10.15252/msb.202110335
摘要
Antibiotic resistance threatens our ability to treat infectious diseases, spurring interest in alternative antimicrobial technologies. The use of bacterial conjugation to deliver CRISPR-cas systems programmed to precisely eliminate antibiotic-resistant bacteria represents a promising approach but requires high in situ DNA transfer rates. We have optimized the transfer efficiency of conjugative plasmid TP114 using accelerated laboratory evolution. We hence generated a potent conjugative delivery vehicle for CRISPR-cas9 that can eliminate > 99.9% of targeted antibiotic-resistant Escherichia coli in the mouse gut microbiota using a single dose. We then applied this system to a Citrobacter rodentium infection model, achieving full clearance within four consecutive days of treatment.
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