Department of Microbiology, University of Pennsylvania, Philadelphia, PA 19104, USA.
Department of Pathology and Laboratory Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA; Department of Physiology, University of Pennsylvania, Philadelphia, PA 19104, USA.
Cell Rep. 2013 Dec 26;5(6):1737-48. doi: 10.1016/j.celrep.2013.11.028. Epub 2013 Dec 12.
Alphaviruses are a large class of insect-borne human pathogens and little is known about the host-factor requirements for infection. To identify such factors, we performed a genome-wide RNAi screen using model Drosophila cells and validated 94 genes that impacted infection of Sindbis virus (SINV), the prototypical alphavirus. We identified a conserved role for SEC61A and valosin-containing protein (VCP) in facilitating SINV entry in insects and mammals. SEC61A and VCP selectively regulate trafficking of the entry receptor NRAMP2, and loss or pharmacological inhibition of these proteins leads to altered NRAMP2 trafficking to lysosomal compartments and proteolytic digestion within lysosomes. NRAMP2 is the major iron transporter in cells, and loss of NRAMP2 attenuates intracellular iron transport. Thus, this study reveals genes and pathways involved in both infection and iron homeostasis that may serve as targets for antiviral therapeutics or for iron-imbalance disorders.
甲病毒是一大类通过昆虫传播的人类病原体,对于其感染所需的宿主因素知之甚少。为了鉴定这些因素,我们使用模型果蝇细胞进行了全基因组 RNAi 筛选,并验证了影响辛德毕斯病毒(SINV)感染的 94 个基因,SINV 是典型的甲病毒。我们发现 SEC61A 和包含缬氨酸的蛋白(VCP)在促进昆虫和哺乳动物中 SINV 进入方面具有保守作用。SEC61A 和 VCP 选择性地调节进入受体 NRAMP2 的运输,这些蛋白质的缺失或药理学抑制会导致 NRAMP2 向溶酶体区室的运输和溶酶体中的蛋白水解消化发生改变。NRAMP2 是细胞中主要的铁转运蛋白,NRAMP2 的缺失会减弱细胞内铁的转运。因此,这项研究揭示了感染和铁稳态相关的基因和途径,它们可能成为抗病毒治疗或铁失衡疾病的靶点。