Long Q X, Wang X Z, Xie W D, He D F, Lan D A, Pang Y, Su D M, Pu Z L
Research Institute of Entomology, Zhongshan University, Guangzhou, Guangdong, China.
Chin J Biotechnol. 1991;7(1):51-61.
The gene coding for the hepatitis B virus surface antigen (HBsAg) under the control of Autographa californicanuclear polyhedrosis virus polyhedrin promoter was successfully inserted into the genome of the Trichoplusia ni nuclear polyhdrosis virus. Infection of Spodoptera frugiperda cells with this recombinant virus produced a significant amount of HBsAg protein and secreted 22 nm particles containing the HBsAg. The expression of HBsAg gene was also obtained both in Trichoplusia ni larvae and in Philosamia cynthia ricini prepupae when infected with the recombinant virus. The HBsAg proteins expressed by baculovirus vector systems have morphological and antigenic properties identical to the 22 nm particles secreted by human cells.
在苜蓿银纹夜蛾核型多角体病毒多角体蛋白启动子的控制下,编码乙肝病毒表面抗原(HBsAg)的基因成功插入到粉纹夜蛾核型多角体病毒的基因组中。用这种重组病毒感染草地贪夜蛾细胞可产生大量HBsAg蛋白,并分泌出含有HBsAg的22纳米颗粒。用重组病毒感染粉纹夜蛾幼虫和蓖麻蚕预蛹时,也获得了HBsAg基因的表达。杆状病毒载体系统表达的HBsAg蛋白具有与人细胞分泌的22纳米颗粒相同的形态和抗原特性。