| Literature DB >> 27066743 |
Avraham Bayer1, Nicholas J Lennemann2, Yingshi Ouyang1, John C Bramley2, Stefanie Morosky2, Ernesto Torres De Azeved Marques3, Sara Cherry4, Yoel Sadovsky5, Carolyn B Coyne6.
Abstract
During mammalian pregnancy, the placenta acts as a barrier between the maternal and fetal compartments. The recently observed association between Zika virus (ZIKV) infection during human pregnancy and fetal microcephaly and other anomalies suggests that ZIKV may bypass the placenta to reach the fetus. This led us to investigate ZIKV infection of primary human trophoblasts (PHTs), which are the barrier cells of the placenta. We discovered that PHT cells from full-term placentas are refractory to ZIKV infection. In addition, medium from uninfected PHT cells protects non-placental cells from ZIKV infection. PHT cells constitutively release the type III interferon (IFN) IFNλ1, which functions in both a paracrine and autocrine manner to protect trophoblast and non-trophoblast cells from ZIKV infection. Our data suggest that for ZIKV to access the fetal compartment, it must evade restriction by trophoblast-derived IFNλ1 and other trophoblast-specific antiviral factors and/or use alternative strategies to cross the placental barrier.Entities:
Keywords: IFNλ; Zika virus; placenta; trophoblasts; type III interferon; virus
Mesh:
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Year: 2016 PMID: 27066743 PMCID: PMC4866896 DOI: 10.1016/j.chom.2016.03.008
Source DB: PubMed Journal: Cell Host Microbe ISSN: 1931-3128 Impact factor: 21.023