Stollar V
Department of Molecular Genetics and Microbiology, University of Medicine and Dentistry of New Jersey, Robert Wood Johnson Medical School, Piscataway 08854.
In Vitro Cell Dev Biol Anim. 1993 Apr;29A(4):289-95. doi: 10.1007/BF02633957.
Alphatogaviruses, of which Sindbis virus (SV) is the prototype, replicate to high titer in the laboratory both in mosquito cells and in vertebrate cells. By studying the replication of SV in mosquito cells as well as in vertebrate cells, we were able to obtain several viral mutants which have novel phenotypes and have contributed to our basic knowledge of this virus family. These include three host range mutants: SVAP15/21 which replicates normally in mosquito cells but is restricted in vertebrate cells and SVCL35 and SVCL58, which are restricted in mosquito cells but replicate normally in vertebrate cells. As well, two other mutants are described here: SVLM21, which can replicate in methionine-starved mosquito cells and SVMPA, which can replicate in mosquito cells treated with mycophenolic acid or ribavirin. The causal mutations of both SVLM21 and SVMPA are within the sequence encoding the nonstructural protein nsPl; these and other findings have enabled us to associate the capping and methylation of the viral mRNAs with the nsPl protein. Our work serves to emphasize that it is both worthwhile and important to study the replication of arthropod-borne viruses in cells derived from the arthropod host as well as in cells derived from the vertebrate host.
α- togaviruses属病毒,其中辛德毕斯病毒(SV)为原型病毒,在实验室中可在蚊细胞和脊椎动物细胞中高效复制。通过研究SV在蚊细胞以及脊椎动物细胞中的复制过程,我们获得了几种具有新表型的病毒突变体,这些突变体增进了我们对该病毒家族的基础知识的了解。其中包括三个宿主范围突变体:SVAP15/21在蚊细胞中能正常复制,但在脊椎动物细胞中受到限制;SVCL35和SVCL58在蚊细胞中受到限制,但在脊椎动物细胞中能正常复制。此外,本文还描述了另外两个突变体:SVLM21能在蛋氨酸饥饿的蚊细胞中复制,SVMPA能在经霉酚酸或利巴韦林处理的蚊细胞中复制。SVLM21和SVMPA的致病突变均位于编码非结构蛋白nsPl的序列内;这些发现以及其他研究结果使我们能够将病毒mRNA的加帽和甲基化与nsPl蛋白联系起来。我们的工作旨在强调,研究节肢动物传播病毒在节肢动物宿主来源的细胞以及脊椎动物宿主来源的细胞中的复制过程是有价值且重要的。