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本文引用的文献

1
Adaptive strategies of the influenza virus polymerase for replication in humans.流感病毒聚合酶在人体中复制的适应策略。
Proc Natl Acad Sci U S A. 2009 Dec 15;106(50):21312-6. doi: 10.1073/pnas.0911915106. Epub 2009 Dec 7.
2
In vitro and in vivo characterization of new swine-origin H1N1 influenza viruses.新型猪源H1N1流感病毒的体外和体内特性研究
Nature. 2009 Aug 20;460(7258):1021-5. doi: 10.1038/nature08260.
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Emergence and pandemic potential of swine-origin H1N1 influenza virus.猪源H1N1流感病毒的出现及大流行潜力
Nature. 2009 Jun 18;459(7249):931-9. doi: 10.1038/nature08157.
4
Single mutation at the amino acid position 627 of PB2 that leads to increased virulence of an H5N1 avian influenza virus during adaptation in mice can be compensated by multiple mutations at other sites of PB2.PB2蛋白第627位氨基酸的单突变会导致H5N1禽流感病毒在适应小鼠的过程中毒力增强,而PB2其他位点的多个突变可以补偿这种增强。
Virus Res. 2009 Sep;144(1-2):123-9. doi: 10.1016/j.virusres.2009.04.008. Epub 2009 Apr 23.
5
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.
6
Human HA and polymerase subunit PB2 proteins confer transmission of an avian influenza virus through the air.人类的血凝素(HA)和聚合酶亚基PB2蛋白可使禽流感病毒通过空气传播。
Proc Natl Acad Sci U S A. 2009 Mar 3;106(9):3366-71. doi: 10.1073/pnas.0813172106. Epub 2009 Feb 11.
7
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.
8
PB2 protein of a highly pathogenic avian influenza virus strain A/chicken/Yamaguchi/7/2004 (H5N1) determines its replication potential in pigs.高致病性禽流感病毒A/鸡/山口/7/2004(H5N1)株的PB2蛋白决定其在猪体内的复制潜力。
J Virol. 2009 Feb;83(4):1572-8. doi: 10.1128/JVI.01879-08. Epub 2008 Dec 3.
9
Growth of H5N1 influenza A viruses in the upper respiratory tracts of mice.甲型H5N1流感病毒在小鼠上呼吸道中的生长情况。
PLoS Pathog. 2007 Oct 5;3(10):1374-9. doi: 10.1371/journal.ppat.0030133.
10
The molecular basis of the pathogenicity of the Dutch highly pathogenic human influenza A H7N7 viruses.荷兰高致病性甲型H7N7人流感病毒致病性的分子基础。
J Infect Dis. 2007 Jul 15;196(2):258-65. doi: 10.1086/518792. Epub 2007 Jun 4.

在 PB2 蛋白 627 位的赖氨酸取代不会改变 2009 年大流行 H1N1 病毒在小鼠中的毒力。

Substitution of lysine at 627 position in PB2 protein does not change virulence of the 2009 pandemic H1N1 virus in mice.

机构信息

International Institute of Infection and Immunity, Shantou University Medical College, Shantou, Guangdong 515031, PR China.

出版信息

Virology. 2010 May 25;401(1):1-5. doi: 10.1016/j.virol.2010.02.024. Epub 2010 Mar 19.

DOI:10.1016/j.virol.2010.02.024
PMID:20303563
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4034467/
Abstract

A lysine at the 627 position (627K) of PB2 protein of influenza virus has been recognized as a determinant for host adaptation and a virulent element for some influenza viruses. While seasonal influenza viruses exclusively contained 627K, the pandemic (H1N1) 2009 possessed a glutamic acid (627E), even after circulation in humans for more than 6months. To explore the potential role of E627K substitution in PB2 in the pandemic (H1N1) 2009 virus, we compared pathogenicity and growth properties between a recombinant virus containing 627K PB2 gene and the parental A/California/4/2009 strain containing 627E. Our results showed that substitution of 627K in PB2 gene does not confer higher virulence and growth rate for the pandemic (H1N1) 2009 virus in mice and cell culture respectively, suggesting 627K is not required for human adaptation of the pandemic (H1N1) 2009 virus.

摘要

流感病毒 PB2 蛋白第 627 位的赖氨酸(627K)已被认为是宿主适应性和一些流感病毒毒力的决定因素。虽然季节性流感病毒仅含有 627K,但大流行性(H1N1)2009 病毒具有谷氨酸(627E),即使在人类中传播了 6 个多月。为了探讨 PB2 中 E627K 取代在大流行性(H1N1)2009 病毒中的潜在作用,我们比较了含有 627K PB2 基因的重组病毒与含有 627E 的亲本 A/California/4/2009 株之间的致病性和生长特性。我们的结果表明,PB2 基因中 627K 的取代并没有赋予大流行性(H1N1)2009 病毒在小鼠和细胞培养中更高的毒力和生长速度,这表明 627K 不是大流行性(H1N1)2009 病毒适应人类的必需条件。