Laboratório de Imunofarmacologia, Instituto Oswaldo Cruz (IOC), Fundação Oswaldo Cruz (Fiocruz), Rio de Janeiro, RJ, Brazil.
Instituto Nacional de Infectologia (INI), Fiocruz, Rio de Janeiro, RJ, Brazil.
Sci Rep. 2017 Jan 18;7:40920. doi: 10.1038/srep40920.
Zika virus (ZIKV) is a member of the Flaviviridae family, along with other agents of clinical significance such as dengue (DENV) and hepatitis C (HCV) viruses. Since ZIKV causes neurological disorders during fetal development and in adulthood, antiviral drugs are necessary. Sofosbuvir is clinically approved for use against HCV and targets the protein that is most conserved among the members of the Flaviviridae family, the viral RNA polymerase. Indeed, we found that sofosbuvir inhibits ZIKV RNA polymerase, targeting conserved amino acid residues. Sofosbuvir inhibited ZIKV replication in different cellular systems, such as hepatoma (Huh-7) cells, neuroblastoma (SH-Sy5y) cells, neural stem cells (NSC) and brain organoids. In addition to the direct inhibition of the viral RNA polymerase, we observed that sofosbuvir also induced an increase in A-to-G mutations in the viral genome. Together, our data highlight a potential secondary use of sofosbuvir, an anti-HCV drug, against ZIKV.
Zika 病毒(ZIKV)属于黄病毒科,与其他具有临床意义的病原体如登革热(DENV)和丙型肝炎(HCV)病毒一起。由于 ZIKV 在胎儿发育和成年期会引起神经紊乱,因此需要抗病毒药物。索非布韦已被临床批准用于治疗 HCV,其作用靶点是黄病毒科成员中最保守的蛋白,即病毒 RNA 聚合酶。事实上,我们发现索非布韦可以抑制 ZIKV RNA 聚合酶,针对保守的氨基酸残基。索非布韦可以抑制不同细胞系统中的 ZIKV 复制,如肝癌(Huh-7)细胞、神经母细胞瘤(SH-Sy5y)细胞、神经干细胞(NSC)和脑类器官。除了直接抑制病毒 RNA 聚合酶外,我们还观察到索非布韦还会诱导病毒基因组中 A 到 G 的突变增加。总之,我们的数据突出了一种抗 HCV 药物索非布韦对抗 ZIKV 的潜在次要用途。