Bragazzi Cunha Juliana, Wobus Christiane E
Department of Microbiology and Immunology, University of Michigan Medical School, Ann Arbor, MI 48109-5620, USA.
Department of Microbiology and Immunology, University of Michigan Medical School, Ann Arbor, MI 48109-5620, USA.
Virus Res. 2016 Aug 15;222:64-70. doi: 10.1016/j.virusres.2016.06.001. Epub 2016 Jun 2.
Noroviruses cause gastroenteritis in humans and other animals, are shed in the feces, and spread through the fecal-oral route. Host cellular expression of attachment and entry receptors for noroviruses is thought to be a key determinant of cell tropism and the strict species-specificity. However, to date, only carbohydrates have been identified as attachment receptors for noroviruses. Thus, we investigated whether host cellular proteins play a role during the early steps of norovirus infection. We used murine norovirus (MNV) as a representative norovirus, since MNV grows well in tissue culture and is a frequently used model to study basic aspects of norovirus biology. Virus overlay protein binding assay followed by tandem mass spectrometry analysis was performed in two permissive cell lines, RAW264.7 (murine macrophages) and SRDC (murine dendritic cells) to identify four cellular membrane proteins as candidates. Loss-of-function studies revealed that CD36 and CD44 promoted MNV-1 binding to primary dendritic cells, while CD98 heavy chain (CD98) and transferrin receptor 1 (TfRc) facilitated MNV-1 binding to RAW 264.7 cells. Furthermore, the VP1 protruding domain of MNV-1 interacted directly with the extracellular domains of recombinant murine CD36, CD98 and TfRc by ELISA. Additionally, MNV-1 infection of RAW 264.7 cells was enhanced by soluble rCD98 extracellular domain. These studies demonstrate that multiple membrane proteins can promote efficient MNV-1 infection in a cell type-specific manner. Future studies are needed to determine the molecular mechanisms by which each of these proteins affect the MNV-1 infectious cycle.
诺如病毒可导致人类和其他动物患肠胃炎,通过粪便排出,并经粪口途径传播。诺如病毒附着和进入受体的宿主细胞表达被认为是细胞嗜性和严格物种特异性的关键决定因素。然而,迄今为止,仅碳水化合物被鉴定为诺如病毒的附着受体。因此,我们研究了宿主细胞蛋白在诺如病毒感染早期阶段是否发挥作用。我们使用鼠诺如病毒(MNV)作为代表性的诺如病毒,因为MNV在组织培养中生长良好,是研究诺如病毒生物学基本方面常用的模型。在两种允许性细胞系RAW264.7(鼠巨噬细胞)和SRDC(鼠树突状细胞)中进行病毒覆盖蛋白结合试验,随后进行串联质谱分析,以鉴定四种细胞膜蛋白作为候选蛋白。功能丧失研究表明,CD36和CD44促进MNV-1与原代树突状细胞结合,而CD98重链(CD98)和转铁蛋白受体1(TfRc)促进MNV-1与RAW 264.7细胞结合。此外,通过ELISA检测发现,MNV-1的VP1突出结构域与重组鼠CD36、CD98和TfRc的胞外结构域直接相互作用。此外,可溶性rCD98胞外结构域增强了RAW 264.7细胞对MNV-1的感染。这些研究表明,多种膜蛋白可以以细胞类型特异性的方式促进MNV-1的有效感染。未来需要开展研究以确定这些蛋白各自影响MNV-1感染周期的分子机制。