Whitehead Institute for Biomedical Research, Cambridge, MA 02142.
Program in Developmental and Stem Cell Biology, The Hospital for Sick Children, Toronto, ON M5G 0A4, Canada.
Proc Natl Acad Sci U S A. 2019 May 7;116(19):9527-9532. doi: 10.1073/pnas.1900867116. Epub 2019 Apr 24.
Zika virus (ZIKV) is a neurotropic and neurovirulent arbovirus that has severe detrimental impact on the developing human fetal brain. To date, little is known about the factors required for ZIKV infection of human neural cells. We identified ZIKV host genes in human pluripotent stem cell (hPSC)-derived neural progenitors (NPs) using a genome-wide CRISPR-Cas9 knockout screen. Mutations of host factors involved in heparan sulfation, endocytosis, endoplasmic reticulum processing, Golgi function, and interferon activity conferred resistance to infection with the Uganda strain of ZIKV and a more recent North American isolate. Host genes essential for ZIKV replication identified in human NPs also provided a low level of protection against ZIKV in isogenic human astrocytes. Our findings provide insights into host-dependent mechanisms for ZIKV infection in the highly vulnerable human NP cells and identify molecular targets for potential therapeutic intervention.
寨卡病毒(ZIKV)是一种神经亲和性和神经毒力的虫媒病毒,对发育中的人类胎儿大脑有严重的不利影响。迄今为止,人们对寨卡病毒感染人类神经细胞所需的因素知之甚少。我们使用全基因组 CRISPR-Cas9 敲除筛选技术,在人多能干细胞(hPSC)衍生的神经祖细胞(NPs)中鉴定出寨卡病毒宿主基因。参与肝素硫酸化、内吞作用、内质网加工、高尔基体功能和干扰素活性的宿主因子的突变赋予了对乌干达株寨卡病毒和最近的北美分离株的感染抗性。在人 NPs 中鉴定出的对寨卡病毒复制至关重要的宿主基因也为同源性人类星形胶质细胞中的寨卡病毒提供了低水平的保护。我们的研究结果为寨卡病毒在高度脆弱的人 NP 细胞中的感染提供了宿主依赖性机制的深入了解,并确定了潜在治疗干预的分子靶点。