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Inhibition of influenza A virus reproduction by a ribozyme targeted against PB1 mRNA.

机译:靶向PB1 mRNA的核酶对甲型流感病毒繁殖的抑制作用。

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摘要

A ribozyme gene directed at a specific cleavage of mRNA coding for PB1 protein, a component of RNA-dependent RNA-polymerase of influenza A virus, was constructed. The avian adenovirus CELO virus-associated RNA (VA RNA CELO) promoter and human cytomegalovirus (CMV) promoter were used for the permanent expression of the ribozyme in cell lines. The cells were infected with influenza A virus strains A/Singapore/1/57 and A/WSN/33, and the suppression of the virus reproduction and virus-specific protein synthesis was measured. The maximal level of the inhibition of virus reproduction as compared to the reproduction in non-transformed cells was 93.5%. Defective recombinant adenoviruses were constructed carrying the genes of functional and non-functional ribozymes under the control of human cytomegalovirus (CMV) promoter. The reproduction of A/WSN/33 virus in CV-1 cells preinfected with recombinant adenoviruses was shown to be suppressed.
机译:构建了针对特定编码PB1蛋白的mRNA的特定切割的核酶基因,PB1蛋白是甲型流感病毒的RNA依赖性RNA聚合酶的组成部分。禽腺病毒CELO病毒相关RNA(VA RNA CELO)启动子和人巨细胞病毒(CMV)启动子被用于核酶在细胞系中的永久表达。用A型流感病毒株A /新加坡/ 1/57和A / WSN / 33感染细胞,并测量对病毒繁殖和病毒特异性蛋白合成的抑制。与未转化细胞中的繁殖相比,抑制病毒繁殖的最大水平为93.5%。构建了在人巨细胞病毒(CMV)启动子控制下携带功能性和非功能性核酶基因的缺陷重组腺病毒。重组腺病毒预感染的CV-1细胞中A / WSN / 33病毒的繁殖显示受到抑制。

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