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首页> 外文期刊>Proceedings of the National Academy of Sciences of the United States of America >Sequence of the 1918 pandemic influenza virus nonstructural gene (NS) segment and characterization of recombinant viruses bearing the 1918 NS genes
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Sequence of the 1918 pandemic influenza virus nonstructural gene (NS) segment and characterization of recombinant viruses bearing the 1918 NS genes

机译:1918年大流行性流感病毒非结构基因(NS)片段的序列和表征携带​​1918 NS基因的重组病毒

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摘要

The influenza A virus pandemic of 1918--1919 resulted in an estimated 20--40 million deaths worldwide. The hemagglutinin and neuraminidase sequences of the 1918 virus were previously determined. We here report the sequence of the A/Brevig Mission/ 1/18 (H1N1) virus nonstructural (NS) segment encoding two pro- teins. NS1 and nuclear export protein. Phylogenetically. these genes appear to be close to the common ancestor of subsequent human and classical swine strain NS genes. Recently, the influenza A virus NS1 protein was shown to be a type I IFN antagonist that plays an important role in viral pathogenesis. By using the recently developed technique of generating influenza A viruses entirely from c1oned cDNAs, the hypothesis that the 1918 virus NS1 gene played a role in virulence was tested in a mouse model. In a BSL3+ laboratory. viruses were generated that possessed either the 1918 NS1 gene alone or the entire 1918 NS segment in a background of influenza A/WSN/33 (H1 N1), a mouse-adapted virus derived from a human influenza strain first isolated in 1933. These 1918 NS viruses replicated well in tissue culture but were attenuated in mice as compared with the isogenic control viruses. This attenuation in mice may be related to the human origin of the 1918 NS1 gene. These results suggest that interaction of the NS1 protein with host-cell factors plays a significant role in viral pathogenesis.
机译:1918--1919年的甲型流感病毒大流行导致全世界估计20--40百万人死亡。先前已经确定了1918年病毒的血凝素和神经氨酸酶序列。我们在这里报告了编码两种蛋白质的A / Brevig Mission / 1/18(H1N1)病毒非结构(NS)段的序列。 NS1和核输出蛋白。在系统发育上。这些基因似乎与后来的人类和经典猪品系NS基因的共同祖先很接近。最近,甲型流感病毒NS1蛋白被证明是I型IFN拮抗剂,在病毒的发病机理中起着重要的作用。通过使用最近开发的完全从克隆的cDNA产生甲型流感病毒的技术,在小鼠模型中测试了1918病毒NS1基因在毒力中起作用的假设。在BSL3 +实验室中。在甲型流感病毒/ WSN / 33(H1 N1)的背景下,产生了仅具有1918 NS1基因或整个1918 NS片段的病毒,这是一种适应小鼠的病毒,源自于1933年首次分离出的人流感毒株。这些1918年与等基因对照病毒相比,NS病毒在组织培养中复制良好,但在小鼠中减毒。小鼠体内的这种衰减可能与1918 NS1基因的人类起源有关。这些结果表明NS1蛋白与宿主细胞因子的相互作用在病毒发病机理中起着重要作用。

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