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用于抗病毒活性测定的编码纳米荧光素酶的重组狂犬病病毒的产生。

Generation of recombinant rabies viruses encoding NanoLuc luciferase for antiviral activity assays.

作者信息

Anindita Paulina Duhita, Sasaki Michihito, Nobori Haruaki, Sato Akihiko, Carr Michael, Ito Naoto, Sugiyama Makoto, Orba Yasuko, Sawa Hirofumi

机构信息

Division of Molecular Pathobiology, Research Center for Zoonosis Control, Hokkaido University, Sapporo, Japan.

Division of Molecular Pathobiology, Research Center for Zoonosis Control, Hokkaido University, Sapporo, Japan; Discovery Research Laboratory for Core Therapeutic Areas, Shionogi & Co., Ltd., Osaka, Japan.

出版信息

Virus Res. 2016 Apr 2;215:121-8. doi: 10.1016/j.virusres.2016.02.002. Epub 2016 Feb 8.

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.

摘要

狂犬病是由狂犬病病毒(RABV)引起的一种致死性疾病,RABV属于弹状病毒科狂犬病毒属。一旦发生中枢神经系统感染并出现症状,尽管有暴露后预防措施,病死率仍接近100%。因此,迫切需要新的狂犬病抗病毒疗法。可以通过筛选小分子化合物来鉴定能够抑制病毒复制的抗病毒药物,然而,由于RABV感染在体外不会产生易于识别的细胞病变效应,细胞活力测定可能无法用于观察小分子化合物对RABV的抗病毒活性。在本研究中,构建了编码纳米荧光素酶(NanoLuc)的重组狂犬病病毒(rRABV)以促进小分子化合物文库的筛选。在病毒感染的单步生长曲线中证实了NanoLuc的表达,结果表明rRABV能够进行病毒复制,并且经过十次连续传代后荧光素酶活性没有降低。此外,rRABV能够在体外定量核苷类似物利巴韦林对RABV的抗病毒活性。这些发现证实了编码NanoLuc的rRABV系统在促进筛选抑制RABV感染的小分子化合物方面的潜力。

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