| Literature DB >> 27565347 |
Laura J Yockey1, Luis Varela2, Tasfia Rakib1, William Khoury-Hanold1, Susan L Fink3, Bernardo Stutz2, Klara Szigeti-Buck2, Anthony Van den Pol4, Brett D Lindenbach5, Tamas L Horvath2, Akiko Iwasaki6.
Abstract
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 (IFNAR) 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.Entities:
Keywords: antiviral defense; female reproductive tract; flavivirus; innate immunity; mucosal immunity; pattern recognition receptors; sexually transmitted infections; type I interferons
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Year: 2016 PMID: 27565347 PMCID: PMC5006689 DOI: 10.1016/j.cell.2016.08.004
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582