| Literature DB >> 26869397 |
Paulina Duhita Anindita1, Michihito Sasaki1, Haruaki Nobori2, Akihiko Sato2, Michael Carr3, Naoto Ito4, Makoto Sugiyama4, Yasuko Orba1, Hirofumi Sawa5.
Abstract
Rabies is an invariably fatal disease caused by Rabies virus (RABV), a member of the family Rhabdoviridae, genus Lyssavirus. Once central nervous infection occurs and symptoms develop, the case fatality rate approaches 100% despite availability of post-exposure prophylaxis. Therefore, new antiviral therapies for rabies are urgently required. Antivirals which can inhibit virus replication can be identified through screening of small compounds, however, as RABV infection does not generate easily discernible cytopathic effects in vitro, cell viability assays may not be feasible to observe antiviral activity of small compounds against RABV. In this study, recombinant RABVs (rRABVs) encoding NanoLuc luciferase (NanoLuc) were generated to facilitate the screening of small compound libraries. NanoLuc expression was confirmed in single-step growth cures of virus infection and showed that the rRABVs were capable of viral replication without decrease of luciferase activity through ten serial passages. Furthermore, the rRABVs were able to quantify the antiviral activity of the nucleoside analogue ribavirin against RABV in vitro. These findings confirm the potential of the rRABV encoding NanoLuc system to facilitate screening of small compounds to inhibit RABV infection.Entities:
Keywords: Antiviral assay; NanoLuc luciferase; Recombinant rabies virus
Mesh:
Substances:
Year: 2016 PMID: 26869397 DOI: 10.1016/j.virusres.2016.02.002
Source DB: PubMed Journal: Virus Res ISSN: 0168-1702 Impact factor: 3.303