复制子
清脆的
生物
病毒复制
病毒学
登革热病毒
基因
寄主因子
计算生物学
病毒
遗传学
核糖核酸
登革热
寄主(生物学)
宿主因子
RNA干扰
辛德比斯病毒
RNA病毒
基因敲除
病毒进化
病毒生命周期
RNA提取
CRISPR干扰
作者
Kai Cheng,Madhura Bhave,Andrew L. Markhard,Duo Peng,Karan Bhatt,Katherine Travisano,Josette Medicielo,Astrid Anaya,Sanae Lembirik,Leila Njoya,Manu Anantpadma,Jens H. Kuhn,Andreas S. Puschnik,Amy Kistler
标识
DOI:10.1038/s41467-025-65979-3
摘要
We describe a viral replicon-based CRISPR knockout (KO) screening approach to specifically identify host factors essential for viral replication which are often missed in live virus screens. We benchmark the replicon screening using a stable fluorescent dengue virus type 2 (DENV-2) replicon cell line and successfully identify host genes known to be required for viral DENV-2 replication (e.g., endoplasmic reticulum membrane complex and oligosaccharyltransferase complex components), along with additional genes that have not been reported in prior CRISPR KO screens with DENV-2. We extend this replicon screening approach to chikungunya virus (CHIKV), a positive-sense RNA virus, and Ebola virus (EBOV), a negative-sense RNA virus, and identify distinct sets of genes required for replication of each virus. Our findings indicate that viral replicon-based CRISPR screens are a useful approach to identify host factors essential for replication of diverse viruses and to elucidate potential novel targets for host-directed medical countermeasures.
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