首页> 美国卫生研究院文献>Journal of Virology >Spontaneous and Engineered Deletions in the 3′ Noncoding Region of Tick-Borne Encephalitis Virus: Construction of Highly Attenuated Mutants of a Flavivirus
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Spontaneous and Engineered Deletions in the 3′ Noncoding Region of Tick-Borne Encephalitis Virus: Construction of Highly Attenuated Mutants of a Flavivirus

机译:Tick-Borne脑炎病毒3非编码区的自发和工程缺失:黄病毒高度减毒突变体的构建。

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摘要

The flavivirus genome is a positive-strand RNA molecule containing a single long open reading frame flanked by noncoding regions (NCR) that mediate crucial processes of the viral life cycle. The 3′ NCR of tick-borne encephalitis (TBE) virus can be divided into a variable region that is highly heterogeneous in length among strains of TBE virus and in certain cases includes an internal poly(A) tract and a 3′-terminal conserved core element that is believed to fold as a whole into a well-defined secondary structure. We have now investigated the genetic stability of the TBE virus 3′ NCR and its influence on viral growth properties and virulence. We observed spontaneous deletions in the variable region during growth of TBE virus in cell culture and in mice. These deletions varied in size and location but always included the internal poly(A) element of the TBE virus 3′ NCR and never extended into the conserved 3′-terminal core element. Subsequently, we constructed specific deletion mutants by using infectious cDNA clones with the entire variable region and increasing segments of the core element removed. A virus mutant lacking the entire variable region was indistinguishable from wild-type virus with respect to cell culture growth properties and virulence in the mouse model. In contrast, even small extensions of the deletion into the core element led to significant biological effects. Deletions extending to nucleotides 10826, 10847, and 10870 caused distinct attenuation in mice without measurable reduction of cell culture growth properties, which, however, were significantly restricted when the deletion was extended to nucleotide 10919. An even larger deletion (to nucleotide 10994) abolished viral viability. In spite of their high degree of attenuation, these mutants efficiently induced protective immune responses even at low inoculation doses. Thus, 3′-NCR deletions represent a useful technique for achieving stable attenuation of flaviviruses that can be included in the rational design of novel flavivirus live vaccines.
机译:黄病毒基因组是一个正链RNA分子,包含一个单一的长开放阅读框,其两侧是介导病毒生命周期关键过程的非编码区(NCR)。 tick传性脑炎(TBE)病毒的3'NCR可分为TBE病毒株之间长度高度异质的可变区,在某些情况下,它包括内部多聚A区和3'端保守的核心元素被认为可以整体折叠成定义​​明确的二级结构。现在我们已经研究了TBE病毒3'NCR的遗传稳定性及其对病毒生长特性和毒力的影响。我们在细胞培养和小鼠中观察到TBE病毒生长过程中可变区的自发缺失。这些缺失的大小和位置各不相同,但始终包含TBE病毒3'NCR的内部poly(A)元素,并且从未延伸到保守的3'-末端核心元素中。随后,我们通过使用感染性cDNA克隆构建了特定的缺失突变体,该克隆具有完整的可变区和增加的核心元件片段。就小鼠模型中的细胞培养物生长特性和毒力而言,缺少整个可变区的病毒突变体与野生型病毒没有区别。相比之下,即使将缺失扩展到核心元件中,也会导致重大的生物学效应。缺失扩展到核苷酸10826、10847和10870会在小鼠中引起明显的衰减,而细胞培养物的生长特性却没有明显降低,但是,当缺失扩展到核苷酸10919时,其显着受到限制。甚至更大的缺失(至核苷酸10994)被废除了。病毒生存力。尽管它们的减毒程度很高,这些突变体即使在低接种剂量下也能有效诱导保护性免疫反应。因此,3'-NCR缺失代表了一种稳定的黄病毒稳定减毒的有用技术,该技术可包括在新型黄病毒活疫苗的合理设计中。

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