Ito N, Takayama M, Yamada K, Sugiyama M, Minamoto N
Department of Veterinary Public Health, Faculty of Agriculture, Gifu University, Gifu 501-1193, Japan.
J Virol. 2001 Oct;75(19):9121-8. doi: 10.1128/JVI.75.19.9121-9128.2001.
In order to identify the viral gene related to the pathogenicity of rabies virus, we tried to establish a reverse genetics system of the attenuated RC-HL strain, which causes nonlethal infection in adult mice after intracerebral inoculation. A full-length genome plasmid encoding the complete antigenomic cDNA of the RC-HL strain and helper plasmids containing cDNAs of the complete open reading frame of the N, P, and L genes, respectively, were constructed. After transfection of these plasmids into BHK-21 cells infected with the T7 RNA polymerase-expressing vaccinia virus, infectious rabies virus with almost the same biological properties as those of the wild-type RC-HL strain was rescued. Using this reverse genetics system of the RC-HL strain, we generated a chimeric virus with the open reading frame of the glycoprotein gene from the parent Nishigahara strain, which kills adult mice after intracerebral inoculation, in the background of the RC-HL genome. Since the chimeric virus killed adult mice following intracerebral inoculation, it became evident that the open reading frame of the glycoprotein gene is related to the pathogenicity of the Nishigahara strain for adult mice.
为了鉴定与狂犬病病毒致病性相关的病毒基因,我们试图建立减毒RC-HL株的反向遗传学系统,该毒株脑内接种成年小鼠后引起非致死性感染。构建了编码RC-HL株完整反基因组cDNA的全长基因组质粒以及分别包含N、P和L基因完整开放阅读框cDNA的辅助质粒。将这些质粒转染到感染表达T7 RNA聚合酶的痘苗病毒的BHK-21细胞中后,拯救出了生物学特性与野生型RC-HL株几乎相同的传染性狂犬病病毒。利用RC-HL株的这一反向遗传学系统,我们构建了一种嵌合病毒,其糖蛋白基因的开放阅读框来自亲本西原株,在RC-HL基因组背景下,该毒株脑内接种成年小鼠后可致其死亡。由于该嵌合病毒脑内接种后可致成年小鼠死亡,因此很明显糖蛋白基因的开放阅读框与西原株对成年小鼠的致病性有关。