Lee Young-Min, Tscherne Donna M, Yun Sang-Im, Frolov Ilya, 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 10021, USA.
J Virol. 2005 Mar;79(6):3231-42. doi: 10.1128/JVI.79.6.3231-3242.2005.
For many viruses, primary infection has been shown to prevent superinfection by a homologous second virus. In this study, we investigated superinfection exclusion of bovine viral diarrhea virus (BVDV), a positive-sense RNA pestivirus. Cells acutely infected with BVDV were protected from superinfection by homologous BVDV but not with heterologous vesicular stomatitis virus. Superinfection exclusion was established within 30 to 60 min but was lost upon passaging of persistently infected cells. Superinfecting BVDV failed to deliver a translatable genome into acutely infected cells, indicating a block in viral entry. Deletion of structural protein E2 from primary infecting BVDV abolished this exclusion. Bypassing the entry block by RNA transfection revealed a second block at the level of replication but not translation. This exclusion did not require structural protein expression and was inversely correlated with the level of primary BVDV RNA replication. These findings suggest dual mechanisms of pestivirus superinfection exclusion, one at the level of viral entry that requires viral glycoprotein E2 and a second at the level of viral RNA replication.
对于许多病毒而言,已证实初次感染可阻止同源性第二种病毒的重复感染。在本研究中,我们调查了牛病毒性腹泻病毒(BVDV)的重复感染排除情况,BVDV是一种正义RNA瘟病毒。急性感染BVDV的细胞可免受同源性BVDV的重复感染,但不能免受异源性水疱性口炎病毒的重复感染。重复感染排除在30至60分钟内确立,但在持续感染细胞传代后丧失。重复感染的BVDV未能将可翻译的基因组递送至急性感染的细胞中,表明病毒进入受阻。从初次感染的BVDV中缺失结构蛋白E2可消除这种排除作用。通过RNA转染绕过进入障碍后,在复制水平而非翻译水平发现了第二个障碍。这种排除不需要结构蛋白表达,并且与初次BVDV RNA复制水平呈负相关。这些发现提示瘟病毒重复感染排除的双重机制,一种在病毒进入水平,需要病毒糖蛋白E2,另一种在病毒RNA复制水平。