| Literature DB >> 33887282 |
Rafaela Sachetto Fernandes1, Andre Schutzer de Godoy2, Igor Andrade Santos3, Gabriela Dias Noske2, Ketllyn Irene Zagato de Oliveira2, Victor Oliveira Gawriljuk2, Ana Carolina Gomes Jardim3, Glaucius Oliva2.
Abstract
The 2015/16 Zika virus (ZIKV) epidemic led to almost 1 million confirmed cases in 84 countries and was associated to the development of congenital microcephaly and Guillain-Barré syndrome. More recently, a ZIKV African lineage was identified in Brazil raising concerns about a future outbreak. The long-term consequences of viral infection emphasizes the need for the development of effective anti-ZIKV drugs. In this study, we developed and characterized a ZIKV replicon cell line for the screening of viral replication inhibitors. The replicon system was developed by engineering the IRES-Neo cassette into the 3' UTR terminus of the ZIKV Rluc DNA construct. After in vitro transcription, replicon RNA was used to transfect BHK-21 cells, that were selected with G418, thus generating the BHK-21-RepZIKV_IRES-Neo cell line. Through this replicon-based cell system, we identified two molecules with potent anti-ZIKV activities, an imidazonaphthyridine and a riminophenazine, both from the MMV/DNDi Pandemic Response Box library of 400 drug-like compounds. The imidazonaphthyridine, known as RO8191, showed remarkable selectivity against ZIKV, while the riminophenazine, the antibiotic Clofazimine, could act as a non-nucleoside analog inhibitor of viral RNA-dependent RNA polymerase (RdRp), as evidenced both in vitro and in silico. The data showed herein supports the use of replicon-based assays in high-throughput screening format as a biosafe and reliable tool for antiviral drug discovery.Entities:
Keywords: Antiviral screening; Clofazimine; Drug discovery; RO8191; Replicon; Zika
Mesh:
Substances:
Year: 2021 PMID: 33887282 DOI: 10.1016/j.virusres.2021.198388
Source DB: PubMed Journal: Virus Res ISSN: 0168-1702 Impact factor: 3.303