Tscherne Donna M, Evans Matthew J, Macdonald Margaret R, Rice Charles M
Laboratory of Virology and Infectious Diseases, Center for the Study of Hepatitis C, The Rockefeller University, 1230 York Avenue, New York, NY 10065, USA.
J Virol. 2008 Mar;82(5):2427-36. doi: 10.1128/JVI.02158-07. Epub 2007 Dec 19.
Bovine viral diarrhea virus (BVDV) is a positive-strand RNA virus and a member of the genus Pestivirus in the family Flaviviridae. To identify and characterize essential factors required for BVDV replication, a library expressing random fragments of the BVDV genome was screened for sequences that act as transdominant inhibitors of viral replication by conferring resistance to cytopathic BVDV-induced cell death. We isolated a BVDV-nonpermissive MDBK cell clone that harbored a 1.2-kb insertion spanning the carboxy terminus of the envelope glycoprotein 1 (E1), the envelope glycoprotein E2, and the amino terminus of p7. Confirming the resistance phenotype conferred by this library clone, naïve MDBK cells expressing this fragment were found to be 100- to 1,000-fold less permissive to both cytopathic and noncytopathic BVDV infection compared to parental MDBK cells, although these cells remained fully permissive to vesicular stomatitis virus. This restriction could be overcome by electroporation of BVDV RNA, indicating a block at one or more steps in viral entry prior to translation of the viral RNA. We determined that the E2 ectodomain was responsible for the inhibition to BVDV entry and that this block occurred downstream from BVDV interaction with the cellular receptor CD46 and virus binding, suggesting interference with a yet-unidentified BVDV entry factor.
牛病毒性腹泻病毒(BVDV)是一种正链RNA病毒,属于黄病毒科瘟病毒属。为了鉴定和表征BVDV复制所需的关键因子,通过赋予对细胞病变性BVDV诱导的细胞死亡的抗性,筛选了一个表达BVDV基因组随机片段的文库,以寻找作为病毒复制反式显性抑制剂的序列。我们分离出一个BVDV非允许性MDBK细胞克隆,该克隆含有一个1.2 kb的插入片段,跨越包膜糖蛋白1(E1)的羧基末端、包膜糖蛋白E2和p7的氨基末端。证实该文库克隆赋予的抗性表型,发现表达该片段的原始MDBK细胞对细胞病变性和非细胞病变性BVDV感染的允许性比亲代MDBK细胞低100至1000倍,尽管这些细胞对水疱性口炎病毒仍完全允许。通过电穿孔BVDV RNA可以克服这种限制,这表明在病毒RNA翻译之前的病毒进入的一个或多个步骤中存在阻断。我们确定E2胞外域负责对BVDV进入的抑制,并且这种阻断发生在BVDV与细胞受体CD46相互作用和病毒结合的下游,表明干扰了一个尚未鉴定的BVDV进入因子。