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A peptide-based viral inactivator inhibits Zika virus infection in pregnant mice and fetuses

机译:基于肽的病毒灭活剂可抑制孕妇和胎儿的寨卡病毒感染

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摘要

Zika virus (ZIKV), a re-emerging flavivirus associated with neurological disorders, has spread rapidly to more than 70 countries and territories. However, no specific vaccines or antiviral drugs are currently available to prevent or treat ZIKV infection. Here we report that a synthetic peptide derived from the stem region of ZIKV envelope protein, designated Z2, potently inhibits infection of ZIKV and other flaviviruses in vitro. We show that Z2 interacts with ZIKV surface protein and disrupts the integrity of the viral membrane. Z2 can penetrate the placental barrier to enter fetal tissues and is safe for use in pregnant mice. Intraperitoneal administration of Z2 inhibits vertical transmission of ZIKV in pregnant C57BL/6 mice and protects type I or type I/II interferon receptor-deficient mice against lethal ZIKV challenge. Thus, Z2 has potential to be further developed as an antiviral treatment against ZIKV infection in high-risk populations, particularly pregnant women.
机译:Zika病毒(ZIKV)是一种与神经系统疾病相关的再出现的黄病毒,已迅速传播到70多个国家和地区。但是,目前尚无用于预防或治疗ZIKV感染的特定疫苗或抗病毒药物。在这里,我们报告说,源自ZIKV包膜蛋白茎区域的合成肽(称为Z2)在体外可有效抑制ZIKV和其他黄病毒的感染。我们显示Z2与ZIKV表面蛋白相互作用并破坏病毒膜的完整性。 Z2可以穿透胎盘屏障进入胎儿组织,并且在怀孕小鼠中安全使用。 Z2的腹膜内给药可抑制ZIKV在孕妇C57BL / 6小鼠中的垂直传播,并保护I型或I / II型干扰素受体缺陷型小鼠免于致命的ZIKV攻击。因此,Z2有潜力进一步发展为针对高风险人群(尤其是孕妇)的ZIKV感染的抗病毒治疗。

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