Type III Interferons Produced by Human Placental Trophoblasts Confer Protection against Zika Virus Infection

被引:417
作者
Bayer, Avraham [1 ,2 ]
Lennemann, Nicholas J. [3 ]
Ouyang, Yingshi [1 ,2 ]
Bramley, John C. [3 ]
Morosky, Stefanie [3 ]
De Azeved Marques, Ernesto Torres, Jr. [4 ,5 ]
Cherry, Sara [6 ]
Sadovsky, Yoel [1 ,2 ,3 ]
Coyne, Carolyn B. [1 ,2 ,3 ]
机构
[1] Univ Pittsburgh, Magee Womens Res Inst, Pittsburgh, PA 15213 USA
[2] Univ Pittsburgh, Dept Obstet Gynecol & Reprod Sci, Pittsburgh, PA 15213 USA
[3] Univ Pittsburgh, Dept Microbiol & Mol Genet, Pittsburgh, PA 15219 USA
[4] Univ Pittsburgh, Ctr Vaccine Res, Pittsburgh, PA 15261 USA
[5] Fundacao Osvaldo Cruz FIOCRUZ, BR-50670420 Recife, PE, Brazil
[6] Univ Penn, Dept Microbiol, Philadelphia, PA 19104 USA
关键词
IN-VITRO; LAMBDA; BRAIN; DIFFERENTIATION; BRAZIL; CELLS;
D O I
10.1016/j.chom.2016.03.008
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
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) IFN lambda 1, 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 IFNl1 and other trophoblast-specific antiviral factors and/or use alternative strategies to cross the placental barrier.
引用
收藏
页码:705 / 712
页数:8
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