Department of Clinical and Biological Sciences, Laboratory of Molecular Virology and Antiviral Research, University of Turin, S. Luigi Gonzaga Hospital, Orbassano Turin, Italy.
Department of Drug Science and Technology, Innovative Pharmaceutical and Cosmetic Technology and Nanotechnology Group, University of Turin, Italy.
Antiviral Res. 2019 Mar;163:29-33. doi: 10.1016/j.antiviral.2019.01.005. Epub 2019 Jan 14.
Zika virus (ZIKV) is an emerging infectious viral pathogen associated with severe fetal cerebral anomalies and the paralytic Guillain-Barrè syndrome in adults. It was the cause of a recent global health crisis following its entrance into a naïve population in the Americas. Nowadays, no vaccine or specific antiviral against ZIKV is available. In this study, we identified three polyoxometalates (POMs), the Anderson-Evans type [TeWO] (TeW), and the Keggin-type [TiWCoO]_ (TiWCo), and [TiPWO] (TiPW), that inhibit ZIKV infection with ECs in the low micromolar range. TiPW, the POM with the greatest selectivity index (SI), was selected and the step of ZIKV replicative cycle putatively inhibited was investigated by specific antiviral assays. We demonstrated that TiPW targets the entry process of ZIKV infection and it is able to significantly reduce ZIKV progeny production. These results suggest that the polyanion TiPW could be a good starting point to develop an effective therapeutic to treat ZIKV infection.
寨卡病毒(ZIKV)是一种新兴的传染性病毒病原体,与严重的胎儿大脑异常和成人的麻痹性格林-巴利综合征有关。在进入美洲的幼稚人群后,它引起了最近的一次全球卫生危机。目前,尚无针对 ZIKV 的疫苗或特定抗病毒药物。在这项研究中,我们鉴定了三种多金属氧酸盐(POM),即安德森-埃文斯型[TeWO](TeW)、Keggin 型[TiWCoO] _(TiWCo)和[TiPWO](TiPW),它们以低微摩尔浓度抑制 ZIKV 感染 ECs。选择了具有最大选择性指数(SI)的 POM TiPW,并通过特定的抗病毒测定研究了推定抑制 ZIKV 复制周期的步骤。我们证明 TiPW 靶向 ZIKV 感染的进入过程,并且能够显著减少 ZIKV 后代的产生。这些结果表明,多阴离子 TiPW 可能是开发有效治疗 ZIKV 感染的治疗方法的良好起点。