Sumiyoshi H, Tignor G H, Shope R E
Department of Epidemiology and Public Health, Yale University School of Medicine, New Haven, Connecticut, USA.
J Infect Dis. 1995 May;171(5):1144-51. doi: 10.1093/infdis/171.5.1144.
Six recombinant Japanese encephalitis virus (JEV) isolates were recovered from infectious RNAs transcribed by T7 RNA polymerase from molecularly cloned cDNA templates. Three of the recombinant viruses had characteristics similar to the wild-type parent virus, JaOArS982. The other 3 recombinant viruses exhibited an attenuated phenotype in mice. An avirulent recombinant virus, IC47, was characterized and compared with the wild-type parent virus and a virulent recombinant virus, IC37. IC47 produced smaller plaques than parent or IC37 viruses and exhibited no viremia or neuroinvasion in young adult mice inoculated subcutaneously and no mortality when inoculated intracerebrally. IC47 was also immunogenic and protective in the murine model. The probable basis for attenuation, revealed by nucleotide sequence analysis, was a single amino acid substitution at position 138 (Glu to Lys) in the E protein.
从T7 RNA聚合酶从分子克隆的cDNA模板转录的感染性RNA中获得了六种重组日本脑炎病毒(JEV)分离株。其中三种重组病毒具有与野生型亲本病毒JaOArS982相似的特征。另外3种重组病毒在小鼠中表现出减毒表型。对一种无毒重组病毒IC47进行了特性鉴定,并与野生型亲本病毒和一种有毒重组病毒IC37进行了比较。IC47产生的蚀斑比亲本或IC37病毒小,在皮下接种的年轻成年小鼠中未出现病毒血症或神经侵袭,脑内接种时也未导致死亡。IC47在小鼠模型中也具有免疫原性和保护性。核苷酸序列分析揭示的减毒可能基础是E蛋白第138位的单个氨基酸取代(Glu变为Lys)。