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A single mutation in the prM protein of Zika virus contributes to fetal microcephaly.

Ling YuanXing-Yao HuangZhong-Yu LiuFeng ZhangXing-Liang ZhuJiu-Yang YuXue JiYan-Peng XuGuanghui LiCui LiHong-Jiang WangYong-Qiang DengMenghua WuMeng-Li ChengQing YeDong-Yang XieXiao-Feng LiXiangxi WangWeifeng ShiBao-Yang HuPei-Yong ShiZhiheng XuCheng-Feng Qin
Published in: Science (New York, N.Y.) (2017)
Zika virus (ZIKV) has evolved into a global health threat because of its unexpected causal link to microcephaly. Phylogenetic analysis reveals that contemporary epidemic strains have accumulated multiple substitutions from their Asian ancestor. Here we show that a single serine-to-asparagine substitution [Ser139→Asn139 (S139N)] in the viral polyprotein substantially increased ZIKV infectivity in both human and mouse neural progenitor cells (NPCs) and led to more severe microcephaly in the mouse fetus, as well as higher mortality rates in neonatal mice. Evolutionary analysis indicates that the S139N substitution arose before the 2013 outbreak in French Polynesia and has been stably maintained during subsequent spread to the Americas. This functional adaption makes ZIKV more virulent to human NPCs, thus contributing to the increased incidence of microcephaly in recent ZIKV epidemics.
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