SUMMARY Emerging evidence from the current outbreak of Zika virus indicates a strong causal link between zika and microcephaly. To investigate how ZIKV infection leads to microcephaly, we used human embryonic stem cell derived cerebral organoids to recapitulate early stage, first trimester fetal brain development. Here we show that a prototype strain of ZIKV, MR766, efficiently infects organoids and causes a decrease in overall organoid size that correlates with the kinetics of viral copy number. The innate immune receptor Toll-like-Receptor 3 TLR3) was up regulated after of human organoidsand mouse neurospheres and TLR3 inhibition reduced the phenotypic effects of ZIKV infection. Pathway analysis expression changes during TLR3 activation highlighted 41 genes also related to neuronal development, suggesting a mechanistic connection to disrupted neurogenesis. Together, therefore, our findings identify a link between ZIKV-mediated TLR3 activation, perturbed cellfate, and a reduction in organoid volume reminiscent of microcephaly