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本文引用的文献

1
Coronavirus pathogenesis and the emerging pathogen severe acute respiratory syndrome coronavirus.冠状病毒发病机制与新出现的病原体严重急性呼吸综合征冠状病毒。
Microbiol Mol Biol Rev. 2005 Dec;69(4):635-64. doi: 10.1128/MMBR.69.4.635-664.2005.
2
Why are HIV-1 fusion inhibitors not effective against SARS-CoV? Biophysical evaluation of molecular interactions.为何HIV-1融合抑制剂对SARS-CoV无效?分子相互作用的生物物理评估。
Biochim Biophys Acta. 2006 Jan;1760(1):55-61. doi: 10.1016/j.bbagen.2005.10.001. Epub 2005 Oct 28.
3
Protease-mediated enhancement of severe acute respiratory syndrome coronavirus infection.蛋白酶介导的严重急性呼吸综合征冠状病毒感染增强作用。
Proc Natl Acad Sci U S A. 2005 Aug 30;102(35):12543-7. doi: 10.1073/pnas.0503203102. Epub 2005 Aug 22.
4
Inhibitors of cathepsin L prevent severe acute respiratory syndrome coronavirus entry.组织蛋白酶L抑制剂可阻止严重急性呼吸综合征冠状病毒进入。
Proc Natl Acad Sci U S A. 2005 Aug 16;102(33):11876-81. doi: 10.1073/pnas.0505577102. Epub 2005 Aug 4.
5
Imaging individual retroviral fusion events: from hemifusion to pore formation and growth.对单个逆转录病毒融合事件进行成像:从半融合到孔形成及生长
Proc Natl Acad Sci U S A. 2005 Jun 14;102(24):8728-33. doi: 10.1073/pnas.0501864102. Epub 2005 Jun 3.
6
The many mechanisms of viral membrane fusion proteins.病毒膜融合蛋白的多种机制。
Curr Top Microbiol Immunol. 2005;285:25-66. doi: 10.1007/3-540-26764-6_2.
7
Severe acute respiratory syndrome.严重急性呼吸综合征
Nat Med. 2004 Dec;10(12 Suppl):S88-97. doi: 10.1038/nm1143.
8
Cellular entry of the SARS coronavirus.严重急性呼吸综合征冠状病毒的细胞进入
Trends Microbiol. 2004 Oct;12(10):466-72. doi: 10.1016/j.tim.2004.08.008.
9
Severe acute respiratory syndrome coronavirus (SARS-CoV) infection inhibition using spike protein heptad repeat-derived peptides.利用刺突蛋白七肽重复序列衍生肽抑制严重急性呼吸综合征冠状病毒(SARS-CoV)感染
Proc Natl Acad Sci U S A. 2004 Jun 1;101(22):8455-60. doi: 10.1073/pnas.0400576101. Epub 2004 May 18.
10
Intracellular targeting signals contribute to localization of coronavirus spike proteins near the virus assembly site.细胞内靶向信号有助于冠状病毒刺突蛋白在病毒组装位点附近定位。
J Virol. 2004 Jun;78(11):5913-22. doi: 10.1128/JVI.78.11.5913-5922.2004.

禽冠状病毒传染性支气管炎病毒在进入宿主细胞的过程中经历直接的低pH值依赖性融合激活。

The avian coronavirus infectious bronchitis virus undergoes direct low-pH-dependent fusion activation during entry into host cells.

作者信息

Chu Victor C, McElroy Lisa J, Chu Vicky, Bauman Beverley E, Whittaker Gary R

机构信息

Dept. of Microbiology and Immunology, College of Veterinary Medicine, Cornell University, Ithaca, NY 14853, USA.

出版信息

J Virol. 2006 Apr;80(7):3180-8. doi: 10.1128/JVI.80.7.3180-3188.2006.

DOI:10.1128/JVI.80.7.3180-3188.2006
PMID:16537586
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1440383/
Abstract

Coronaviruses are the causative agents of respiratory disease in humans and animals, including severe acute respiratory syndrome. Fusion of coronaviruses is generally thought to occur at neutral pH, although there is also evidence for a role of acidic endosomes during entry of a variety of coronaviruses. Therefore, the molecular basis of coronavirus fusion during entry into host cells remains incompletely defined. Here, we examined coronavirus-cell fusion and entry employing the avian coronavirus infectious bronchitis virus (IBV). Virus entry into cells was inhibited by acidotropic bases and by other inhibitors of pH-dependent endocytosis. We carried out fluorescence-dequenching fusion assays of R18-labeled virions and show that for IBV, coronavirus-cell fusion occurs in a low-pH-dependent manner, with a half-maximal rate of fusion occurring at pH 5.5. Fusion was reduced, but still occurred, at lower temperatures (20 degrees C). We observed no effect of inhibitors of endosomal proteases on the fusion event. These data are the first direct measure of virus-cell fusion for any coronavirus and demonstrate that the coronavirus IBV employs a direct, low-pH-dependent virus-cell fusion activation reaction. We further show that IBV was not inactivated, and fusion was unaffected, by prior exposure to pH 5.0 buffer. Virions also showed evidence of reversible conformational changes in their surface proteins, indicating that aspects of the fusion reaction may be reversible in nature.

摘要

冠状病毒是人类和动物呼吸道疾病的病原体,包括严重急性呼吸综合征。冠状病毒的融合通常被认为发生在中性pH值条件下,尽管也有证据表明酸性内体在多种冠状病毒进入过程中发挥作用。因此,冠状病毒进入宿主细胞过程中融合的分子基础仍未完全明确。在此,我们利用禽冠状病毒传染性支气管炎病毒(IBV)研究了冠状病毒与细胞的融合及进入过程。病毒进入细胞受到亲酸性碱和其他pH依赖性内吞作用抑制剂的抑制。我们对R18标记的病毒粒子进行了荧光猝灭融合试验,结果表明,对于IBV,冠状病毒与细胞的融合以低pH依赖性方式发生,融合半最大速率出现在pH 5.5时。在较低温度(20摄氏度)下,融合减少但仍会发生。我们观察到内体蛋白酶抑制剂对融合事件没有影响。这些数据是对任何冠状病毒病毒与细胞融合的首次直接测量,表明冠状病毒IBV采用直接的、低pH依赖性的病毒与细胞融合激活反应。我们进一步表明,预先暴露于pH 5.0缓冲液不会使IBV失活,且融合不受影响。病毒粒子表面蛋白也显示出可逆构象变化的证据,表明融合反应的某些方面在本质上可能是可逆的。