| Literature DB >> 29288699 |
Jia-Qi Li1, Cheng-Lin Deng2, Dayong Gu3, Xiao Li1, Lei Shi3, Jian'an He3, Qiu-Yan Zhang1, Bo Zhang4, Han-Qing Ye5.
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 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.Entities:
Keywords: Antiviral screening; Flavivirus; Luciferase; Replicon cell line; Zika virus
Mesh:
Substances:
Year: 2017 PMID: 29288699 DOI: 10.1016/j.antiviral.2017.12.017
Source DB: PubMed Journal: Antiviral Res ISSN: 0166-3542 Impact factor: 5.970