Chin K C, Cresswell P
Section of Immunobiology, Howard Hughes Medical Institute, Yale University School of Medicine, 310 Cedar Street, New Haven, CT 06520-8011, USA.
Proc Natl Acad Sci U S A. 2001 Dec 18;98(26):15125-30. doi: 10.1073/pnas.011593298.
Little is known about the mechanism by which IFNs inhibit human cytomegalovirus (HCMV) replication. Indeed, infection of fibroblasts with HCMV initiates the expression of a subset of type I IFN-inducible genes whose role in the infectious process is unclear. We describe here the identification of a cytoplasmic antiviral protein that is induced by IFNs, by HCMV infection, and by the HCMV envelope protein, glycoprotein B (gB). Stable expression of the protein in fibroblasts inhibits productive HCMV infection, down-regulating several HCMV structural proteins (gB, pp28, and pp65) known to be indispensable for viral assembly and maturation. We have named the protein viperin (for virus inhibitory protein, endoplasmic reticulum-associated, interferon-inducible). HCMV infection causes the redistribution of the induced viperin from its normal endoplasmic reticulum association, first to the Golgi apparatus and then to cytoplasmic vacuoles containing gB and pp28. Expression before HCMV infection reduces viperin redistribution from the endoplasmic reticulum to the Golgi apparatus and prevents vacuolar localization, perhaps reflecting the mechanism used by HCMV to evade the antiviral function.
关于干扰素抑制人巨细胞病毒(HCMV)复制的机制,目前所知甚少。实际上,用HCMV感染成纤维细胞会启动一组I型干扰素诱导基因的表达,而这些基因在感染过程中的作用尚不清楚。我们在此描述了一种细胞质抗病毒蛋白的鉴定,该蛋白可由干扰素、HCMV感染以及HCMV包膜蛋白糖蛋白B(gB)诱导产生。该蛋白在成纤维细胞中的稳定表达可抑制HCMV的有效感染,下调几种已知对病毒组装和成熟必不可少的HCMV结构蛋白(gB、pp28和pp65)。我们将该蛋白命名为蝰蛇蛋白(viperin,即病毒抑制蛋白,内质网相关,干扰素诱导)。HCMV感染导致诱导产生的蝰蛇蛋白从其正常的内质网关联部位重新分布,首先转移至高尔基体,然后转移至含有gB和pp28的细胞质液泡中。在HCMV感染之前表达可减少蝰蛇蛋白从内质网到高尔基体的重新分布,并防止其液泡定位,这可能反映了HCMV逃避抗病毒功能所采用的机制。