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Selection of H5N1 influenza virus PB2 during replication in humans.人感染H5N1流感病毒复制过程中PB2基因的选择
J Virol. 2009 May;83(10):5278-81. doi: 10.1128/JVI.00063-09. Epub 2009 Mar 4.
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Transmission of influenza virus in a mammalian host is increased by PB2 amino acids 627K or 627E/701N.PB2蛋白第627位氨基酸为赖氨酸(627K)或谷氨酸(627E)以及第701位氨基酸为天冬酰胺(701N)会增加流感病毒在哺乳动物宿主体内的传播。
PLoS Pathog. 2009 Jan;5(1):e1000252. doi: 10.1371/journal.ppat.1000252. Epub 2009 Jan 2.
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X-ray structure of NS1 from a highly pathogenic H5N1 influenza virus.高致病性H5N1流感病毒NS1的X射线结构
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Evolution of highly pathogenic H5N1 avian influenza viruses in Vietnam between 2001 and 2007.2001年至2007年间越南高致病性H5N1禽流感病毒的演变
PLoS One. 2008;3(10):e3462. doi: 10.1371/journal.pone.0003462. Epub 2008 Oct 21.
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Evolutionary dynamics and emergence of panzootic H5N1 influenza viruses.大流行H5N1流感病毒的进化动态与出现
PLoS Pathog. 2008 Sep 26;4(9):e1000161. doi: 10.1371/journal.ppat.1000161.
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Toward a unified nomenclature system for highly pathogenic avian influenza virus (H5N1).迈向高致病性禽流感病毒(H5N1)统一命名系统。
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Complete genome analysis of a highly pathogenic H5N1 influenza A virus isolated from a tiger in China.对从中国一只老虎身上分离出的高致病性甲型H5N1流感病毒进行全基因组分析。
Arch Virol. 2008;153(8):1569-74. doi: 10.1007/s00705-008-0145-3. Epub 2008 Jul 1.
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Spidermonkey: rapid detection of co-evolving sites using Bayesian graphical models.蜘蛛猴:使用贝叶斯图形模型快速检测共同进化位点
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A new influenza virus virulence determinant: the NS1 protein four C-terminal residues modulate pathogenicity.一种新型流感病毒毒力决定因素:NS1蛋白的四个C末端残基调节致病性。
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10
Virulence of H5N1 avian influenza virus enhanced by a 15-nucleotide deletion in the viral nonstructural gene.H5N1禽流感病毒毒力因病毒非结构基因中15个核苷酸的缺失而增强。
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高致病性禽流感H5N1病毒中哺乳动物毒力决定因素的检测:已发表数据的多变量分析

Detection of mammalian virulence determinants in highly pathogenic avian influenza H5N1 viruses: multivariate analysis of published data.

作者信息

Lycett S J, Ward M J, Lewis F I, Poon A F Y, Kosakovsky Pond S L, Brown A J Leigh

机构信息

Institute of Evolutionary Biology, University of Edinburgh, West Mains Road, Edinburgh EH9 3JT, United Kingdom.

出版信息

J Virol. 2009 Oct;83(19):9901-10. doi: 10.1128/JVI.00608-09. Epub 2009 Jul 22.

DOI:10.1128/JVI.00608-09
PMID:19625397
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2748028/
Abstract

Highly pathogenic avian influenza (HPAI) virus H5N1 infects water and land fowl and can infect and cause mortality in mammals, including humans. However, HPAI H5N1 strains are not equally virulent in mammals, and some strains have been shown to cause only mild symptoms in experimental infections. Since most experimental studies of the basis of virulence in mammals have been small in scale, we undertook a meta-analysis of available experimental studies and used Bayesian graphical models (BGM) to increase the power of inference. We applied text-mining techniques to identify 27 individual studies that experimentally determined pathogenicity in HPAI H5N1 strains comprising 69 complete genome sequences. Amino acid sequence data in all 11 genes were coded as binary data for the presence or absence of mutations related to virulence in mammals or nonconsensus residues. Sites previously implicated as virulence determinants were examined for association with virulence in mammals in this data set, and the sites with the most significant association were selected for further BGM analysis. The analyses show that virulence in mammals is a complex genetic trait directly influenced by mutations in polymerase basic 1 (PB1) and PB2, nonstructural 1 (NS1), and hemagglutinin (HA) genes. Several intra- and intersegment correlations were also found, and we postulate that there may be two separate virulence mechanisms involving particular combinations of polymerase and NS1 mutations or of NS1 and HA mutations.

摘要

高致病性禽流感(HPAI)病毒H5N1可感染水禽和陆禽,并能感染包括人类在内的哺乳动物并导致其死亡。然而,HPAI H5N1毒株在哺乳动物中的毒力并不相同,一些毒株在实验感染中仅引起轻微症状。由于大多数关于哺乳动物毒力基础的实验研究规模较小,我们对现有的实验研究进行了荟萃分析,并使用贝叶斯图形模型(BGM)来增强推断能力。我们应用文本挖掘技术,识别出27项通过实验确定HPAI H5N1毒株致病性的个体研究,这些研究包含69个完整的基因组序列。所有11个基因中的氨基酸序列数据被编码为二进制数据,以表示与哺乳动物毒力相关的突变或非一致性残基的存在或不存在。在此数据集中,检查了先前被认为是毒力决定因素的位点与哺乳动物毒力的关联,并选择了关联最显著的位点进行进一步的BGM分析。分析表明,哺乳动物中的毒力是一种复杂的遗传特征,直接受聚合酶碱性1(PB1)和PB2、非结构1(NS1)以及血凝素(HA)基因中的突变影响。还发现了几个基因片段内和基因片段间的相关性,我们推测可能存在两种独立的毒力机制,分别涉及聚合酶和NS1突变的特定组合或NS1和HA突变的特定组合。