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A Mouse Model of Zika Virus Sexual Transmission and Vaginal Viral Replication

机译:Zika病毒性传播和阴道病毒复制的小鼠模型

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Case reports of Zika virus (ZIKV) sexual transmission and genital persistence are mounting. Venereal transmission and genital persistence threaten public health within and beyond the range of ZIKV's mosquito vectors. In this study, we administered ZIKV into the vaginas of AG129 mice and LysMCre^+IFNAR^f^l^/^f^l C57BL/6 mice after hormonal treatments. Mice infected during estrus-like phase were resistant to vaginal infection. In contrast, when infected during diestrus-like phase, AG129 mice succumbed to infection, whereas LysMCre^+IFNAR^f^l^/^f^l mice experienced transient illness. Patency of transgenital transmission (TGT) in diestrus-like mice was demonstrated by detection of viremia and ZIKV replication in spleen and brain, and viral RNA persisted in vaginal washes as late as 10 days post-infection. In these lethal and sublethal mouse models, this study indicates that intravaginal deposition of ZIKV can cause TGT, hormonal changes in the female reproductive tract (FRT) influence transmission, and ZIKV replication persists in the FRT for several days.
机译:Zika病毒(ZIKV)性传播和生殖器持久性的病例报告正在安装。性传播和生殖器持久性威胁到Zikv蚊子媒介范围内的公共卫生。在这项研究中,我们给予ZIKV成AG129小鼠和LysMCre ^ + IFNAR ^ f的阴道^ L ^ / ^ F ^升C57BL /激素治疗后的6只小鼠。在雌性相位期间感染的小鼠对阴道感染有抗性。相反,当在感染动情样阶段,AG129小鼠死于感染,而LysMCre ^ + IFNAR ^ F ^ L ^ / ^ F ^升小鼠经历短暂的疾病。通过检测脾脏和脑中的病毒血症和ZIKV复制来证明分子性传播(TGT)在病毒血症和ZIKV复制中,病毒RNA在感染后10天晚期持续的病毒RNA。在这些致死和核对鼠标模型中,本研究表明,ZIKV的阴道沉积可能导致TGT,雌性生殖道(FRT)影响变速器的激素变化,ZIKV复制在FRT持续数天。

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