Moss S R, Nuttall P A
Institute of Virology and Environmental Microbiology, Oxford, UK.
Virus Res. 1994 Jun;32(3):401-7. doi: 10.1016/0168-1702(94)90088-4.
The genes encoding the two major core proteins (VP2 and VP7) of Broadhaven (BRD) virus, a tick-borne orbivirus, were inserted into the genome of Autographa californica nuclear polyhedrosis virus (AcNPV) under the control of copies of the AcNPV polyhedrin promoter to produce two recombinant baculoviruses. Infection of Spodoptera frugiperda (Sf) cells with a recombinant AcNPV that synthesized BRDV VP2 produced large numbers of BRDV subcore-like particles. Co-infection of cells with the two recombinants that made either BRDV VP2 or VP7 produced core-like particles similar in appearance to authentic BRDV cores. No evidence was obtained for the formation of core-like particles between the major core proteins of BRDV and those of bluetongue virus (BTV) following the co-expression of BRDV VP2 and BTV VP7, or BRDV VP7 and BTV VP3, indicating that in this respect the proteins of these two orbiviruses are incompatible, unlike the situation previously described for epizootic haemorrhagic disease virus and BTV core proteins.
将蜱传环状病毒布罗德黑文病毒(BRD病毒)的两种主要核心蛋白(VP2和VP7)的编码基因,在苜蓿银纹夜蛾核型多角体病毒(AcNPV)多角体蛋白启动子拷贝的控制下,插入到AcNPV基因组中,以产生两种重组杆状病毒。用合成BRDV VP2的重组AcNPV感染草地贪夜蛾(Sf)细胞,产生了大量BRDV亚核心样颗粒。用产生BRDV VP2或VP7的两种重组体共同感染细胞,产生了外观与正宗BRDV核心相似的核心样颗粒。在共表达BRDV VP2和蓝舌病毒(BTV)VP7,或BRDV VP7和BTV VP3后,未获得BRDV主要核心蛋白与BTV主要核心蛋白之间形成核心样颗粒的证据,这表明在这方面这两种环状病毒的蛋白不相容,这与之前描述的 epizootic haemorrhagic disease virus和BTV核心蛋白的情况不同。