Department of Microbiology and Physiological Systems, University of Massachusetts Medical School, Worcester, MA, USA.
Methods Mol Biol. 2021;2244:247-264. doi: 10.1007/978-1-0716-1111-1_13.
Clustered regularly interspaced short palindromic repeats (CRISPR)/Cas9 screens enable virus-host genetic screens to be undertaken in a more robust manner than previously possible and has had a tremendous impact in the field of virus study. Researchers can take advantage of the power of CRISPR genetic screens to discover virus-host interaction genes including host receptors and signaling molecules (Bazzone et al., mBio 10 (1): e02734-18, 2019; E et al., Proc Natl Acad Sci U S A 116(14):7043-7052, 2019; McDougall et al., Curr Opin Virol 29:87-100, 2018; Savidis et al., Cell Rep 16(1):232-246, 2016). In principle, lysis of cells late in the virus infection cycle allows one to screen for essential genes using pooled single-guide RNAs (sgRNAs) that collective target an entire host cell genome simply by identifying mutant cells that are resistant to virus-induced cell death. Here we focus on using this technique on epithelial cells to identify host targets required for human cytomegalovirus (HCMV) infection.
成簇规律间隔短回文重复序列 (CRISPR)/Cas9 筛选能够以比以往更强大的方式进行病毒-宿主遗传筛选,并且在病毒研究领域产生了巨大的影响。研究人员可以利用 CRISPR 遗传筛选的强大功能来发现病毒-宿主相互作用基因,包括宿主受体和信号分子(Bazzone 等人,mBio 10 (1): e02734-18, 2019;E 等人,Proc Natl Acad Sci U S A 116(14):7043-7052, 2019;McDougall 等人,Curr Opin Virol 29:87-100, 2018;Savidis 等人,Cell Rep 16(1):232-246, 2016)。从原理上讲,在病毒感染周期的后期使细胞裂解,可以通过鉴定对病毒诱导的细胞死亡具有抗性的突变细胞,使用集体靶向整个宿主细胞基因组的池化单指导 RNA (sgRNA) 筛选必需基因。在这里,我们专注于将该技术用于上皮细胞,以鉴定人巨细胞病毒 (HCMV) 感染所需的宿主靶标。