Eloit M, Gilardi-Hebenstreit P, Toma B, Perricaudet M
Laboratoire d'Epidémiologie, INRA, Ecole Nationale Vétérinaire d'Alfort, Maisons-Alfort, France.
J Gen Virol. 1990 Oct;71 ( Pt 10):2425-31. doi: 10.1099/0022-1317-71-10-2425.
The gene encoding the pseudorabies virus glycoprotein gp50 was cloned at the very left end of the genome of adenovirus type 5 to give a recombinant adenovirus (Ad-gp50) defective for the E1A gene. Ad-gp50 expressed high levels of gp50 in cells which either complemented (293 cells) or did not complement (Vero and HeLa cells) the E1A gene. Surprisingly, over an extended period, higher levels of gp50 were produced in HeLa cells which lack the E1A gene. Rabbits and mice inoculated with Ad-gp50 showed a strong antibody response against gp50. Some of them were protected from a virulent challenge with pseudorabies virus.
将编码伪狂犬病病毒糖蛋白gp50的基因克隆到5型腺病毒基因组的最左端,得到一种E1A基因缺陷的重组腺病毒(Ad-gp50)。Ad-gp50在能互补E1A基因的细胞(293细胞)或不能互补E1A基因的细胞(Vero细胞和HeLa细胞)中均高水平表达gp50。令人惊讶的是,在较长一段时间内,缺乏E1A基因的HeLa细胞产生的gp50水平更高。接种Ad-gp50的兔子和小鼠对gp50表现出强烈的抗体反应。其中一些动物受到了伪狂犬病病毒强毒株攻击的保护。