| Article ID | Journal | Published Year | Pages | File Type | 
|---|---|---|---|---|
| 8523377 | Antiviral Research | 2018 | 33 Pages | 
Abstract
												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 Zâ² 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.
											Keywords
												
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											Authors
												Jia-Qi Li, Cheng-Lin Deng, Dayong Gu, Xiao Li, Lei Shi, Jian'an He, Qiu-Yan Zhang, Bo Zhang, Han-Qing Ye, 
											