King A M, Stott E J, Langer S J, Young K K, Ball L A, Wertz G W
J Virol. 1987 Sep;61(9):2885-90. doi: 10.1128/JVI.61.9.2885-2890.1987.
The construction and characterization of vaccinia virus recombinants carrying the nucleocapsid (N) protein gene of human respiratory syncytial (RS) virus are described. Recombinant viruses were constructed that contained the N gene oriented either positively or negatively with respect to the 7.5-kilodalton vaccinia virus promoter. In addition, a positively oriented recombinant was constructed that lacked an out-of-frame AUG codon in the 5'-terminal noncoding region. In HEp-2 cells, both positive-orientation recombinants induced the synthesis of a protein which comigrated with N protein and was precipitated by antisera to RS virus. Sera from mice immunized with these recombinants specifically precipitated the RS virus N protein. Analysis of mRNA and protein expressed from the recombinant N genes showed that deletion of the upstream AUG codon markedly improved the efficiency of protein synthesis. Mice were vaccinated with the high-expressing recombinant and subsequently challenged with live RS virus. The results of these experiments demonstrated that the immune response to N protein afforded a significant degree of protection against RS virus disease.
本文描述了携带人呼吸道合胞(RS)病毒核衣壳(N)蛋白基因的痘苗病毒重组体的构建及特性。构建了重组病毒,其包含相对于7.5千道尔顿痘苗病毒启动子正向或负向排列的N基因。此外,构建了一个正向排列的重组体,该重组体在5'端非编码区缺少一个移码AUG密码子。在HEp-2细胞中,两个正向排列的重组体均诱导合成了一种与N蛋白共迁移且能被抗RS病毒抗血清沉淀的蛋白质。用这些重组体免疫的小鼠血清能特异性沉淀RS病毒N蛋白。对重组N基因表达的mRNA和蛋白质的分析表明,上游AUG密码子的缺失显著提高了蛋白质合成效率。用高表达重组体给小鼠接种疫苗,随后用活RS病毒进行攻击。这些实验结果表明,对N蛋白的免疫反应能提供显著程度的抗RS病毒疾病保护。