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本文引用的文献

1
Genome-wide RNAi screen identifies human host factors crucial for influenza virus replication.全基因组 RNAi 筛选鉴定出流感病毒复制所必需的人类宿主因子。
Nature. 2010 Feb 11;463(7282):818-22. doi: 10.1038/nature08760. Epub 2010 Jan 17.
2
A physical and regulatory map of host-influenza interactions reveals pathways in H1N1 infection.宿主-流感相互作用的物理和调控图谱揭示了 H1N1 感染中的途径。
Cell. 2009 Dec 24;139(7):1255-67. doi: 10.1016/j.cell.2009.12.018.
3
Identification of amino acids in HA and PB2 critical for the transmission of H5N1 avian influenza viruses in a mammalian host.鉴定 HA 和 PB2 中对 H5N1 禽流感病毒在哺乳动物宿主中传播至关重要的氨基酸。
PLoS Pathog. 2009 Dec;5(12):e1000709. doi: 10.1371/journal.ppat.1000709. Epub 2009 Dec 24.
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Human host factors required for influenza virus replication.流感病毒复制所需的人体宿主因素。
Nature. 2010 Feb 11;463(7282):813-7. doi: 10.1038/nature08699.
5
The influence of the multi-basic cleavage site of the H5 hemagglutinin on the attenuation, immunogenicity and efficacy of a live attenuated influenza A H5N1 cold-adapted vaccine virus.H5血凝素多碱性裂解位点对甲型H5N1流感冷适应减毒活疫苗病毒的减毒、免疫原性及效力的影响
Virology. 2009 Dec 20;395(2):280-8. doi: 10.1016/j.virol.2009.09.017. Epub 2009 Oct 14.
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The polymerase acidic protein gene of influenza a virus contributes to pathogenicity in a mouse model.甲型流感病毒的聚合酶酸性蛋白基因在小鼠模型中对致病性有影响。
J Virol. 2009 Dec;83(23):12325-35. doi: 10.1128/JVI.01373-09. Epub 2009 Sep 30.
7
Host genetic variation affects resistance to infection with a highly pathogenic H5N1 influenza A virus in mice.宿主基因变异影响小鼠对高致病性甲型H5N1流感病毒感染的抵抗力。
J Virol. 2009 Oct;83(20):10417-26. doi: 10.1128/JVI.00514-09. Epub 2009 Aug 12.
8
A single-amino-acid substitution in a polymerase protein of an H5N1 influenza virus is associated with systemic infection and impaired T-cell activation in mice.H5N1流感病毒聚合酶蛋白中的单个氨基酸替换与小鼠的全身感染及T细胞活化受损有关。
J Virol. 2009 Nov;83(21):11102-15. doi: 10.1128/JVI.00994-09. Epub 2009 Aug 19.
9
Acquisition of a polybasic hemagglutinin cleavage site by a low-pathogenic avian influenza virus is not sufficient for immediate transformation into a highly pathogenic strain.低致病性禽流感病毒获得多碱性血凝素裂解位点并不足以使其立即转变为高致病性毒株。
J Virol. 2009 Jun;83(11):5864-8. doi: 10.1128/JVI.02649-08. Epub 2009 Mar 18.
10
Host genetic background strongly influences the response to influenza a virus infections.宿主遗传背景对甲型流感病毒感染的反应有强烈影响。
PLoS One. 2009;4(3):e4857. doi: 10.1371/journal.pone.0004857. Epub 2009 Mar 18.

高致病性 A/Vietnam/1203/2004(H5N1)禽流感病毒血凝素的多碱性裂解位点以宿主特异性方式在哺乳动物中充当毒力因子。

The multibasic cleavage site of the hemagglutinin of highly pathogenic A/Vietnam/1203/2004 (H5N1) avian influenza virus acts as a virulence factor in a host-specific manner in mammals.

机构信息

Laboratory of Infectious Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, USA.

出版信息

J Virol. 2012 Mar;86(5):2706-14. doi: 10.1128/JVI.05546-11. Epub 2011 Dec 28.

DOI:10.1128/JVI.05546-11
PMID:22205751
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3302284/
Abstract

Highly pathogenic avian influenza (HPAI) viruses of the H5 and H7 subtypes typically possess multiple basic amino acids around the cleavage site (MBS) of their hemagglutinin (HA) protein, a recognized virulence motif in poultry. To determine the importance of the H5 HA MBS as a virulence factor in mammals, recombinant wild-type HPAI A/Vietnam/1203/2004 (H5N1) viruses that possessed (H5N1) or lacked (ΔH5N1) the H5 HA MBS were generated and evaluated for their virulence in BALB/c mice, ferrets, and African green monkeys (AGMs) (Chlorocebus aethiops). The presence of the H5 HA MBS was associated with lethality, significantly higher virus titers in the respiratory tract, virus dissemination to extrapulmonary organs, lymphopenia, significantly elevated levels of proinflammatory cytokines and chemokines, and inflammation in the lungs of mice and ferrets. In AGMs, neither H5N1 nor ΔH5N1 virus was lethal and neither caused clinical symptoms. The H5 HA MBS was associated with mild enhancement of replication and delayed virus clearance. Thus, the contribution of H5 HA MBS to the virulence of the HPAI H5N1 virus varies among mammalian hosts and is most significant in mice and ferrets and less remarkable in nonhuman primates.

摘要

高致病性禽流感(HPAI)病毒的 H5 和 H7 亚型通常在其血凝素(HA)蛋白的裂解位点(MBS)周围具有多个碱性氨基酸,这是家禽中公认的毒力特征。为了确定 H5 HA MBS 作为哺乳动物中致病因子的重要性,生成了具有(H5N1)或缺乏(ΔH5N1)H5 HA MBS 的重组野生型 HPAI A/Vietnam/1203/2004(H5N1)病毒,并在 BALB/c 小鼠、雪貂和非洲绿猴( Chlorocebus aethiops)中评估了它们的毒力。H5 HA MBS 的存在与致死性相关,呼吸道中的病毒滴度显著升高,病毒向肺外器官传播,淋巴细胞减少,促炎细胞因子和趋化因子水平显著升高,以及小鼠和雪貂肺部的炎症。在非洲绿猴中,H5N1 或 ΔH5N1 病毒均无致死性,也均未引起临床症状。H5 HA MBS 与复制的轻度增强和病毒清除的延迟相关。因此,H5 HA MBS 对 HPAI H5N1 病毒毒力的贡献在不同的哺乳动物宿主中存在差异,在小鼠和雪貂中最为显著,在非人类灵长类动物中则不那么明显。