基因敲除
铜绿假单胞菌
CRISPR干扰
生物
基因沉默
Cas9
清脆的
基因
RNA干扰
计算生物学
遗传学
微生物学
细菌
核糖核酸
作者
Michelle Yu,Amy B. Banta,Ryan D. Ward,Neha K. Prasad,Michael S. Kwon,Oren S. Rosenberg,Jason M. Peters
出处
期刊:Methods in molecular biology
日期:2023-10-11
卷期号:: 13-32
标识
DOI:10.1007/978-1-0716-3473-8_2
摘要
CRISPR interference (CRISPRi) is a robust gene silencing technique that is ideal for targeting essential and conditionally essential (CE) genes. CRISPRi is especially valuable for investigating gene function in pathogens such as P. aeruginosa where essential and CE genes underlie clinically important phenotypes such as antibiotic susceptibility and virulence. To facilitate the use of CRISPRi in diverse bacteria-including P. aeruginosa-we developed a suite of modular, mobilizable, and integrating vectors we call, "Mobile-CRISPRi." We further optimized Mobile-CRISPRi for use in P. aeruginosa mouse models of acute lung infection by expressing the CRISPRi machinery at low levels constitutively, enabling partial knockdown of essential and CE genes without the need for an exogenous inducer. Here, we describe protocols for creating Mobile-CRISPRi knockdown strains and testing their phenotypes in a mouse pneumonia model of P. aeruginosa infection. In addition, we provide comprehensive guide RNA designs to target genes in common laboratory strains of P. aeruginosa and other Pseudomonas species.
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