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In vitro antiviral activity of arbidol against Chikungunya virus and characteristics of a selected resistant mutant.

机译:Arbidol对基孔肯雅病毒的体外抗病毒活性和所选抗性突变体的特征。

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Arbidol (ARB) is an antiviral drug originally licensed in Russia for use against influenza and other respiratory viral infections. Although a broad-spectrum antiviral activity has been reported for this drug, there is until now no data regarding its effects against alphavirus infection. Here, the in vitro antiviral effect of ARB on Chikungunya virus (CHIKV) replication was investigated and this compound was found to present potent inhibitory activity against the virus propagated onto immortalized Vero cells or primary human fibroblasts (MRC-5 lung cells) (IC(50)<10mug/ml). A CHIKV resistant mutant was then selected and adapted to growth in the presence of 30mug/ml ARB in MRC5 cells; its complete sequence analysis revealed a single amino acid substitution (G407R) localized in the E2 envelope protein. To confirm the G407R role in the molecular mechanism of ARB resistance, a CHIKV infectious clone harboring the same substitution was engineered, tested, and was found to display a similar level of resistance. Finally, our results demonstrated the effective in vitro antiviral activity of ARB against CHIKV and gave some tracks to understand the molecular basis of ARB activity.
机译:Arbidol(ARB)是一种抗病毒药,最初在俄罗斯获得许可,可用于对抗流感和其他呼吸道病毒感染。尽管已报道该药物具有广谱抗病毒活性,但迄今为止,尚无有关其抗甲病毒感染的数据。在这里,研究了ARB对基孔肯雅病毒(CHIKV)复制的体外抗病毒作用,发现该化合物对传播到永生化的Vero细胞或原代人成纤维细胞(MRC-5肺细胞)上的病毒具有有效的抑制活性(IC( 50)<10mug / ml)。然后选择一个CHIKV抗性突变体,使其适应MRC5细胞中30mug / ml ARB的生长。它的完整序列分析揭示了位于E2包膜蛋白中的单个氨基酸取代(G407R)。为了证实G407R在抗ARB分子机制中的作用,设计,测试了具有相同取代基的CHIKV传染性克隆,并显示出相似的抗性水平。最后,我们的结果证明了ARB对CHIKV的有效体外抗病毒活性,并提供了一些途径来了解ARB活性的分子基础。

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