Ulper Liane, Sarand Inga, Rausalu Kai, Merits Andres
Estonian Biocentre, Riia Street 23, 51010 Tartu, Estonia.
J Virol Methods. 2008 Mar;148(1-2):265-70. doi: 10.1016/j.jviromet.2007.10.007. Epub 2007 Dec 3.
Semliki Forest virus (SFV, genus Alphavirus) has a broad host range, high efficiency of viral protein expression, and the ability to stimulate an immune response. These properties have made SFV an attractive tool for development of expression vectors, and plasmid clones containing cDNA of the SFV genome often are used. However, instability of these plasmids resulting from cryptic expression of SFV envelope proteins in Escherichia coli represents a problem both for the development of SFV-based vectors and for SFV research. In this study, an infectious plasmid of SFV, pCMV-SFV4, was constructed; its toxic effect was eliminated by intron insertion in the capsid protein encoding region. When transfected into mammalian cells, the plasmid clone was highly infectious and produced virus with properties identical to those of wild-type SFV. The inserted intron was efficiently and properly removed from the RNA genome of SFV. Therefore, this novel and stabilized infectious SFV plasmid represents a superior tool for basic studies of SFV as well as for biotechnological applications.
塞姆利基森林病毒(SFV,甲病毒属)具有广泛的宿主范围、高效的病毒蛋白表达能力以及刺激免疫反应的能力。这些特性使SFV成为开发表达载体的一个有吸引力的工具,并且常使用含有SFV基因组cDNA的质粒克隆。然而,由于SFV包膜蛋白在大肠杆菌中的隐性表达导致这些质粒不稳定,这对基于SFV的载体开发以及SFV研究来说都是一个问题。在本研究中,构建了一种SFV感染性质粒pCMV - SFV4;通过在衣壳蛋白编码区插入内含子消除了其毒性作用。当转染到哺乳动物细胞中时,该质粒克隆具有高度感染性,并产生具有与野生型SFV相同特性的病毒。插入的内含子从SFV的RNA基因组中被有效且正确地去除。因此,这种新型的、稳定的感染性SFV质粒是用于SFV基础研究以及生物技术应用的一种优越工具。