Hurrelbrink Robert J, Nestorowicz Ann, McMinn Peter C
Department of Microbiology, University of Western Australia, Nedlands, WA 6907, Australia1.
Endocrine Division, Lilly Research Laboratories, Indianapolis, IN 46285, USA2.
J Gen Virol. 1999 Dec;80 ( Pt 12):3115-3125. doi: 10.1099/0022-1317-80-12-3115.
An infectious cDNA clone of Murray Valley encephalitis virus prototype strain 1-51 (MVE-1-51) was constructed by stably inserting genome-length cDNA into the low-copy-number plasmid vector pMC18. Designated pMVE-1-51, the clone consisted of genome-length cDNA of MVE-1-51 under the control of a T7 RNA polymerase promoter. The clone was constructed by using existing components of a cDNA library, in addition to cDNA of the 3' terminus derived by RT-PCR of poly(A)-tailed viral RNA. Upon comparison with other flavivirus sequences, the previously undetermined sequence of the 3' UTR was found to contain elements conserved throughout the genus FLAVIVIRUS: RNA transcribed from pMVE-1-51 and subsequently transfected into BHK-21 cells generated infectious virus. The plaque morphology, replication kinetics and antigenic profile of clone-derived virus (CDV-1-51) was similar to the parental virus in vitro. Furthermore, the virulence properties of CDV-1-51 and MVE-1-51 (LD(50) values and mortality profiles) were found to be identical in vivo in the mouse model. Through site-directed mutagenesis, the infectious clone should serve as a valuable tool for investigating the molecular determinants of virulence in MVE virus.
通过将全长cDNA稳定插入低拷贝数质粒载体pMC18,构建了墨累谷脑炎病毒原型株1-51(MVE-1-51)的感染性cDNA克隆。该克隆命名为pMVE-1-51,由T7 RNA聚合酶启动子控制下的MVE-1-51全长cDNA组成。除了通过对聚腺苷酸化病毒RNA进行RT-PCR获得的3'末端cDNA外,该克隆还利用了cDNA文库的现有成分构建而成。与其他黄病毒序列比较后发现,先前未确定的3'UTR序列含有黄病毒属中保守的元件:从pMVE-1-51转录并随后转染到BHK-21细胞中的RNA产生了感染性病毒。克隆衍生病毒(CDV-1-51)的噬斑形态、复制动力学和抗原谱在体外与亲本病毒相似。此外,在小鼠模型中,发现CDV-1-51和MVE-1-51的毒力特性(LD(50)值和死亡率曲线)在体内是相同的。通过定点诱变,该感染性克隆应成为研究MVE病毒毒力分子决定因素的有价值工具。