Levine B, Griffin D E
Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland 21287.
J Virol. 1993 Nov;67(11):6872-5. doi: 10.1128/JVI.67.11.6872-6875.1993.
To understand the role of tissue-specific adaptation and antibody-induced selectional pressures in the evolution of neurovirulent viruses, we analyzed three strains of Sindbis virus isolated from the brains of persistently infected scid mice and four strains of Sindbis virus isolated from the brains of scid mice with viral reactivation following immune serum treatment. For each viral isolate, we tested neurovirulence in weanling BALB/c mice and sequenced regions of the E2 and E1 envelope glycoprotein genes that are known to contain important determinants of Sindbis virus neurovirulence. One strain isolated from a persistently infected scid mouse and two strains isolated from scid mice with viral reactivation were neurovirulent, resulting in mortality in 80 to 100% of weanling BALB/c mice. All three neurovirulent strains contained an A-->U change at nucleotide 8795, which predicts a Gln-->His substitution at E2 amino acid position 55. No nucleotide changes were detected in the other sequenced regions of the E2 and E1 envelope glycoprotein genes or in the avirulent isolates. Our findings indicate that tissue-specific adaptations, rather than antibody-induced selectional pressures, are a critical determinant of the evolution of neurovirulent strains of Sindbis virus and provide evidence that E2 His-55 is an important neuroadaptive mutation that confers neurovirulence properties on Sindbis virus.
为了解组织特异性适应性和抗体诱导的选择压力在神经毒性病毒进化中的作用,我们分析了从持续感染的scid小鼠大脑中分离出的三株辛德毕斯病毒,以及从经免疫血清处理后病毒重新激活的scid小鼠大脑中分离出的四株辛德毕斯病毒。对于每一株病毒分离株,我们在断乳的BALB/c小鼠中测试了神经毒性,并对E2和E1包膜糖蛋白基因中已知包含辛德毕斯病毒神经毒性重要决定因素的区域进行了测序。从持续感染的scid小鼠中分离出的一株病毒和从病毒重新激活的scid小鼠中分离出的两株病毒具有神经毒性,导致80%至100%的断乳BALB/c小鼠死亡。所有三株神经毒性病毒株在核苷酸8795处都有一个A→U的变化,这预测E2氨基酸位置55处有一个Gln→His的替换。在E2和E1包膜糖蛋白基因的其他测序区域或无毒分离株中未检测到核苷酸变化。我们的研究结果表明,组织特异性适应性而非抗体诱导的选择压力是辛德毕斯病毒神经毒性毒株进化的关键决定因素,并提供证据表明E2 His-55是一个重要的神经适应性突变,赋予了辛德毕斯病毒神经毒性特性。