“…ZIKV has an intrinsic tropism for neural stem and progenitor cells (NSCs) in cell cultures, brain organoids and fetal brain slices ( Cugola et al., 2016 ; Dang et al., 2016 ; Garcez et al., 2016 ; Liang et al., 2016 ; Qian et al., 2016 ; Tang et al., 2016 ), whereas ZIKV has much lower infectivity to more differentiated immature or mature neurons ( Li et al., 2016a ; Muffat et al., 2018 ). ZIKV infection impairs NSC proliferation and differentiation, triggers cell death, and results in cerebral developmental delay ( Shao et al., 2016 ; Shao et al., 2017 ; Nielsen-Saines et al., 2019 ; Zeng et al., 2020 ). Notably, mammalian multipotent stem cells, including NSCs, intrinsically produce little interferon (IFN) and response poorly to IFN treatment compare to somatic cells ( Hong and Carmichael, 2013 ; Wu et al., 2019 ), and thus these cells often rely on other machineries once the virus breaches the surveillance ( Ding and Voinnet, 2007 ).…”