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首页> 外文期刊>Journal of Virology >Temperature-sensitive Mutants of Sindbis Virus: Biochemical Correlates of Complementation
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Temperature-sensitive Mutants of Sindbis Virus: Biochemical Correlates of Complementation

机译:Sindbis病毒的温度敏感突变体:互补的生化相关性

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Temperature-sensitive mutants of Sindbis virus fail to grow at a temperature that permits growth of the wild type, but when certain pairs of these mutants, mixed together, infect cells at that temperature, viral growth (i.e., complementation) occurs. The yield from this complementation, however, is of the same order of magnitude as the infectivity in the inoculum. Since in animal virus infections the protein components of the virion probably enter the cell with the viral nucleic acid, it was necessary to demonstrate that the observed complementation required synthesis of new viral protein and nucleic acid rather than some sort of rearrangement of the structural components of the inoculum. To demonstrate that complementation does require new biosynthesis, three biochemical events of normal virus growth have been observed during complementation and correlated with the efficiency of viral growth seen in complementation. These events include: (i) entrance of parental viral ribonucleic acid (RNA) into a double-stranded form; (ii) subsequent synthesis of viral RNA; and (iii) synthesis and subsequent incorporation of viral protein(s) into cell membranes where they were detected by hemadsorption. Although the infecting single-stranded RNA genome of the wild type was converted to a ribonuclease-resistant form, the genome of a mutant (ts-11) incapable of RNA synthesis at a nonpermissive temperature was not so converted. However, during complementation with another mutant also defective in viral RNA synthesis, some of the RNA of mutant ts-11 was converted to a ribonuclease-resistant form, and total synthesis of virus-specific RNA was markedly enhanced. The virus-specific alteration of the cell surface, detected by hemadsorption, was also extensively increased during complementation. These observations support the view that complementation between temperature-sensitive mutants and replication of wild-type virus are similar processes.
机译:Sindbis病毒的温度敏感突变体未能在允许野生型生长的温度下生长,但是当某些这些突变体的成对混合在一起时,在该温度下感染细胞,发生病毒生长(即互补)。然而,这种互补的产量与接种物中的感染性相同的数量级。由于在动物病毒感染中,病毒群岛的蛋白质成分可能与病毒核酸进入细胞,因此必须证明观察到的互补所需的新病毒蛋白和核酸的合成,而不是某种形式的结构部件的重排接种物。为了证明互补确实需要新的生物合成,在互补期间已经观察到在互补期间观察到正常病毒生长的三种生化事件,并与互补中所见的病毒生长效率相关。这些事件包括:(i)父母病毒性核糖核酸(RNA)进入双链形式; (ii)随后的病毒RNA合成; (iii)通过溶血性检测到它们的细胞膜中的合成和随后将病毒蛋白掺入细胞膜中。虽然感染野生型的单链RNA基因组被转化为核糖核酸酶抗性形式,但是在非智能温度下不能RNA合成的突变体( Ts -11)的基因组不是如此转化。然而,在与另一个突变体的互补过程中,在病毒RNA合成中也有缺陷,突变体 TS -11的一些RNA转化为核糖核酸酶抗性形式,并且有病毒特异性RNA的总合成显着增强。通过血液检测到的细胞表面的特异性改变,在互补期间也广泛增加。这些观察结果支持该观点,即温敏突变体和野生型病毒复制之间的互补是类似的过程。

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