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      Vaginal Exposure to Zika Virus during Pregnancy Leads to Fetal Brain Infection

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          SUMMARY

          Zika virus (ZIKV) can be transmitted sexually between humans. However, it is unknown whether ZIKV replicates in the vagina and impacts the unborn fetus. Here, we establish a mouse model of vaginal ZIKV infection and demonstrate that, unlike other routes, ZIKV replicates within the genital mucosa even in wild-type (WT) mice. Mice lacking RNA sensors or transcription factors IRF3 and IRF7 resulted in higher levels of local viral replication. Furthermore, mice lacking the type I interferon (IFN) receptor became viremic and died of infection after a high-dose vaginal ZIKV challenge. Notably, vaginal infection of pregnant dams during early pregnancy led to fetal growth restriction and infection of the fetal brain in WT mice. This was exacerbated in mice deficient in IFN pathways, leading to abortion. Our study highlights the vaginal tract as a highly susceptible site of ZIKV replication and illustrates the dire disease consequences during pregnancy.

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          Author and article information

          Journal
          0413066
          2830
          Cell
          Cell
          Cell
          0092-8674
          1097-4172
          19 August 2016
          25 August 2016
          25 August 2017
          : 166
          : 5
          : 1247-1256.e4
          Affiliations
          [1 ]Department of Immunobiology, Yale University School of Medicine, New Haven, CT, 06520 USA
          [2 ]Program in Integrative Cell Signaling and Neurobiology of Metabolism, Section of Comparative Medicine, Yale University School of Medicine, New Haven, CT, 06520 USA
          [3 ]Department of Laboratory Medicine, Yale University School of Medicine, New Haven, CT, 06520 USA
          [4 ]Department of Neurosurgery, Yale University School of Medicine, New Haven, CT, 06520 USA
          [5 ]Department of Microbial Pathogenesis, Yale University School of Medicine, New Haven, CT, 06520 USA
          [6 ]Howard Hughes Medical Institute, Yale University School of Medicine, New Haven, CT, 06520 USA
          Author notes
          [* ]Correspondence: akiko.iwasaki@ 123456yale.edu
          [7]

          Lead Contact

          Article
          PMC5006689 PMC5006689 5006689 nihpa809515
          10.1016/j.cell.2016.08.004
          5006689
          27565347
          795cb0a9-648a-457c-a584-bf4a50ae2cfe
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