Weyer U, Possee R D
NERC Institute of Virology and Environmental Microbiology, Oxford, U.K.
J Gen Virol. 1991 Dec;72 ( Pt 12):2967-74. doi: 10.1099/0022-1317-72-12-2967.
A baculovirus transfer vector, pAcUW3, was developed to facilitate the insertion of two influenza virus genes, those encoding the haemagglutinin (HA) and neuraminidase (NA) membrane glycoproteins, into the Autographa californica nuclear polyhedrosis virus genome in a single cotransfection experiment. The NA gene was inserted in place of the polyhedrin coding sequences under the control of the polyhedrin promoter, whereas the HA gene was placed under the control of a copy of the p10 promoter at a site upstream of and in opposite orientation to the polyhedrin promoter. After infection of Spodoptera frugiperda cells with the recombinant virus, AcUW3HANA, both HA and NA were expressed in the very late phase of infection and were shown to be functional in appropriate assays. Immunofluorescence assays demonstrated their localization at the surface of infected insect cells. The expression of both foreign genes in the recombinant virus was found to be stable for at least 12 passages in cell culture.
开发了一种杆状病毒转移载体pAcUW3,以便在单次共转染实验中将两个流感病毒基因(即编码血凝素(HA)和神经氨酸酶(NA)膜糖蛋白的基因)插入苜蓿银纹夜蛾核型多角体病毒基因组中。NA基因在多角体蛋白启动子的控制下插入到多角体蛋白编码序列的位置,而HA基因则置于多角体蛋白启动子上游且方向相反的一个p10启动子拷贝的控制之下。用重组病毒AcUW3HANA感染草地贪夜蛾细胞后,HA和NA在感染的极晚期均有表达,并在适当的检测中显示具有功能。免疫荧光检测证明它们定位于受感染昆虫细胞的表面。发现在细胞培养中,重组病毒中外源基因的表达至少在12代内是稳定的。