Marshall J J, Roy P
NERC Institute of Virology and Environmental Microbiology, Oxford, U.K.
Virus Res. 1990 Mar;15(3):189-95. doi: 10.1016/0168-1702(90)90027-9.
DNA representing RNA segments 2 and 5 of bluetongue virus (BTV) serotype 10, corresponding to the genes that code for the outer capsid proteins VP2 and VP5, have been inserted into a baculovirus transfer vector in lieu of the coding region of the polyhedrin gene of Autographa californica nuclear polyhedrosis virus (AcNPV). After co-transfection of Spodoptera frugiperda cells with wild-type AcNPV DNA in the presence of the recombinant transfer vector DNAs polyhedrin-negative recombinant baculoviruses were recovered. When S. frugiperda cells were infected with these recombinant viruses proteins of similar size and antigenic properties to BTV VP2 and VP5 were synthesised. The recombinant VP2, but not the recombinant VP5, was shown to be capable of inducing antibodies that neutralized the infectivity of BTV-10 in vitro.
代表蓝舌病毒10型(BTV-10)RNA片段2和5的DNA,对应于编码外衣壳蛋白VP2和VP5的基因,已被插入杆状病毒转移载体中,取代了苜蓿银纹夜蛾核型多角体病毒(AcNPV)多角体蛋白基因的编码区。在重组转移载体DNA存在的情况下,将野生型AcNPV DNA与草地贪夜蛾细胞共转染后,回收了多角体蛋白阴性的重组杆状病毒。当用这些重组病毒感染草地贪夜蛾细胞时,合成了大小和抗原特性与BTV VP2和VP5相似的蛋白质。结果表明,重组VP2而非重组VP5能够诱导产生在体外中和BTV-10感染性的抗体。