Tautz N, Harada T, Kaiser A, Rinck G, Behrens S, Thiel H J
Institut für Virologie (FB Veterinärmedizin), Justus-Liebig-Universität Giessen, D-35392 Giessen, Germany.
J Virol. 1999 Nov;73(11):9422-32. doi: 10.1128/JVI.73.11.9422-9432.1999.
Defective interfering particles (DIs) of bovine viral diarrhea virus (BVDV) have been identified and shown to be cytopathogenic (cp) in the presence of noncytopathogenic (noncp) helper virus. Moreover, a subgenomic (sg) RNA corresponding in its genome structure to one of those BVDV DIs (DI9) was replication competent in the absence of helper virus. We report here that an sg BVDV replicon which encodes from the viral proteins only the first three amino acids of the autoprotease N(pro) in addition to nonstructural (NS) proteins NS3 to NS5B replicates autonomously and also induces lysis of its host cells. This demonstrates that the presence of a helper virus is not required for the lysis of the host cell. On the basis of two infectious BVDV cDNA clones, namely, BVDV CP7 (cp) and CP7ins- (noncp), bicistronic replicons expressing proteins NS2-3 to NS5B were established. These replicons express, in addition to the viral proteins, the reporter gene encoding beta-glucuronidase; the release of this enzyme from transfected culture cells was used to monitor cell lysis. Applying these tools, we were able to show that the replicon derived from CP7ins- does not induce cell lysis. Accordingly, neither N(pro) nor any of the structural proteins are necessary to maintain the noncp phenotype. Furthermore, these sg RNAs represent the first pair of cp and noncp replicons which mimic complete BVDV CP7 and CP7ins- with respect to cytopathogenicity. These replicons will facilitate future studies aimed at the determination of the molecular basis for the cytopathogenicity of BVDV.
牛病毒性腹泻病毒(BVDV)的缺陷干扰颗粒(DIs)已被鉴定出来,并显示在非细胞病变性(noncp)辅助病毒存在的情况下具有细胞病变性(cp)。此外,一种亚基因组(sg)RNA,其基因组结构与那些BVDV DIs之一(DI9)相对应,在没有辅助病毒的情况下具有复制能力。我们在此报告,一种sg BVDV复制子除了编码非结构(NS)蛋白NS3至NS5B外,仅从病毒蛋白中编码自蛋白酶N(pro)的前三个氨基酸,它能自主复制,还能诱导其宿主细胞裂解。这表明宿主细胞的裂解不需要辅助病毒的存在。基于两个感染性BVDV cDNA克隆,即BVDV CP7(cp)和CP7ins-(noncp),建立了表达蛋白NS2-3至NS5B的双顺反子复制子。这些复制子除了病毒蛋白外,还表达编码β-葡萄糖醛酸酶的报告基因;该酶从转染的培养细胞中的释放被用于监测细胞裂解。应用这些工具,我们能够证明源自CP7ins-的复制子不会诱导细胞裂解。因此,N(pro)和任何结构蛋白对于维持noncp表型都不是必需的。此外,这些sg RNA代表了第一对cp和noncp复制子,它们在细胞病变性方面模拟了完整的BVDV CP7和CP7ins-。这些复制子将有助于未来旨在确定BVDV细胞病变性分子基础的研究。