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本文引用的文献

1
Reassortment between seasonal and swine-origin H1N1 influenza viruses generates viruses with enhanced growth capability in cell culture.季节性和猪源 H1N1 流感病毒之间的重配会产生在细胞培养中具有增强生长能力的病毒。
Virus Res. 2011 Mar;156(1-2):147-50. doi: 10.1016/j.virusres.2010.12.014. Epub 2010 Dec 31.
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High level of genetic compatibility between swine-origin H1N1 and highly pathogenic avian H5N1 influenza viruses.猪源 H1N1 流感病毒和高致病性禽流感 H5N1 病毒之间具有高度的遗传相容性。
J Virol. 2010 Oct;84(20):10918-22. doi: 10.1128/JVI.01140-10. Epub 2010 Aug 4.
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Introduction of virulence markers in PB2 of pandemic swine-origin influenza virus does not result in enhanced virulence or transmission.引入大流行猪源流感病毒 PB2 中的毒力标记不会导致增强的毒力或传播。
J Virol. 2010 Apr;84(8):3752-8. doi: 10.1128/JVI.02634-09. Epub 2010 Feb 3.
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Origins and evolutionary genomics of the 2009 swine-origin H1N1 influenza A epidemic.2009年甲型H1N1猪源流感疫情的起源与进化基因组学
Nature. 2009 Jun 25;459(7250):1122-5. doi: 10.1038/nature08182.
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Emergence of a novel swine-origin influenza A (H1N1) virus in humans.一种新型猪源甲型流感病毒(H1N1)在人类中的出现。
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Compatibility among polymerase subunit proteins is a restricting factor in reassortment between equine H7N7 and human H3N2 influenza viruses.聚合酶亚基蛋白之间的兼容性是马H7N7流感病毒和人H3N2流感病毒重配的一个限制因素。
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Host restriction of avian influenza viruses at the level of the ribonucleoproteins.禽流感病毒在核糖核蛋白水平上的宿主限制
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Genetic compatibility and virulence of reassortants derived from contemporary avian H5N1 and human H3N2 influenza A viruses.源自当代甲型禽流感H5N1和人类H3N2流感病毒的重配病毒的基因兼容性和毒力
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Nuclear traffic of influenza virus proteins and ribonucleoprotein complexes.流感病毒蛋白和核糖核蛋白复合体的核运输
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Generation of influenza A viruses entirely from cloned cDNAs.完全由克隆的互补DNA产生甲型流感病毒。
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季节性 H1N1 和大流行(H1N1)2009 流感病毒之间的重配受到聚合酶亚基之间有限兼容性的限制。

Reassortment between seasonal H1N1 and pandemic (H1N1) 2009 influenza viruses is restricted by limited compatibility among polymerase subunits.

机构信息

Division of Virology, Department of Microbiology and Immunology, The University of Tokyo, Shirokanedai, Minato-ku, Tokyo 108-8639, Japan.

出版信息

J Virol. 2011 Aug;85(16):8449-52. doi: 10.1128/JVI.05054-11. Epub 2011 Jun 15.

DOI:10.1128/JVI.05054-11
PMID:21680507
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3147997/
Abstract

Reassortment is important for influenza virus evolution and the generation of novel viruses with pandemic potential; however, the factors influencing reassortment are still poorly understood. Here, using reverse genetics and a replicon assay, we demonstrated that a mixed polymerase complex containing a pandemic (H1N1) 2009 influenza virus PB2 on a seasonal H1N1 virus background has reduced polymerase activity, leading to impaired virus viability. Adaptation of viruses containing the mixed polymerase complex resulted in compensatory mutations in PB1. Taken together, our results identify the cooperation between PB2 and PB1 as an important restricting factor for reassortment of influenza viruses.

摘要

重配对于流感病毒的进化和具有大流行潜力的新型病毒的产生非常重要;然而,影响重配的因素仍了解甚少。在这里,我们使用反向遗传学和复制子测定法,证明了含有大流行(H1N1)2009 流感病毒 PB2 的混合聚合酶复合物在季节性 H1N1 病毒背景下具有降低的聚合酶活性,导致病毒活力受损。含有混合聚合酶复合物的病毒的适应性导致 PB1 中的补偿性突变。总之,我们的结果确定了 PB2 和 PB1 之间的合作是流感病毒重配的一个重要限制因素。