复制子
寨卡病毒
黄病毒
病毒学
生物
高通量筛选
病毒
生物信息学
遗传学
基因
基因组
作者
Jiaqi Li,Cheng‐Lin Deng,Dayong Gu,Xiao Li,Lei Shi,Jianan He,Qiu‐Yan Zhang,Bo Zhang,Han‐Qing Ye
标识
DOI:10.1016/j.antiviral.2017.12.017
摘要
Zika virus (ZIKV) is an important emerging human pathogen associated with microcephaly, Guillain-Barré syndrome and meningoencephalitis. Developing rapid and reliable HTS assay is important for ZIKV drug discovery. Here, we constructed a dicistronic ZIKV replicon (ZIKV-Pac-Rluc-Rep) that contained the Renilla luciferase (Rluc) reporter gene separated from the puromycin N-acetyl-transferase (Pac) selectable marker by a short peptide cleavage site. A clonal replicon cell line stably expressing high level of ZIKV replicon was established by selection with puromycin. By optimizing cell number, compound concentration and incubation time, a robust replicon cell-based HTS assay was developed with a calculated Z′ value of >0.5. The fully optimized assay was further validated using several known flavivirus replication inhibitors. Altogether, the replicon cell-based HTS assay developed in this study will facilitate the discovery of antiviral compounds against ZIKV.
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