• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

相似文献

1
Filovirus pathogenesis and immune evasion: insights from Ebola virus and Marburg virus.丝状病毒发病机制与免疫逃逸:来自埃博拉病毒和马尔堡病毒的见解
Nat Rev Microbiol. 2015 Nov;13(11):663-76. doi: 10.1038/nrmicro3524. Epub 2015 Oct 6.
2
Evasion of interferon responses by Ebola and Marburg viruses.埃博拉和马尔堡病毒对干扰素反应的逃避。
J Interferon Cytokine Res. 2009 Sep;29(9):511-20. doi: 10.1089/jir.2009.0076.
3
Innate Immune Responses of Bat and Human Cells to Filoviruses: Commonalities and Distinctions.蝙蝠和人类细胞对丝状病毒的固有免疫反应:共性与差异
J Virol. 2017 Mar 29;91(8). doi: 10.1128/JVI.02471-16. Print 2017 Apr 15.
4
Effects of Filovirus Interferon Antagonists on Responses of Human Monocyte-Derived Dendritic Cells to RNA Virus Infection.丝状病毒干扰素拮抗剂对人单核细胞衍生树突状细胞对RNA病毒感染反应的影响。
J Virol. 2016 Apr 29;90(10):5108-5118. doi: 10.1128/JVI.00191-16. Print 2016 May 15.
5
Impact of Měnglà Virus Proteins on Human and Bat Innate Immune Pathways.猛犸病毒蛋白对人类和蝙蝠固有免疫途径的影响。
J Virol. 2020 Jun 16;94(13). doi: 10.1128/JVI.00191-20.
6
Filoviral immune evasion mechanisms.丝状病毒的免疫逃避机制。
Viruses. 2011 Sep;3(9):1634-49. doi: 10.3390/v3091634. Epub 2011 Sep 7.
7
Innate immune evasion by filoviruses.丝状病毒对固有免疫的逃避
Virology. 2015 May;479-480:122-30. doi: 10.1016/j.virol.2015.03.030. Epub 2015 Apr 3.
8
Tissue and cellular tropism, pathology and pathogenesis of Ebola and Marburg viruses.埃博拉病毒和马尔堡病毒的组织和细胞嗜性、病理学和发病机制。
J Pathol. 2015 Jan;235(2):153-74. doi: 10.1002/path.4456.
9
Pathogenesis of filoviral haemorrhagic fevers.丝状病毒出血热的发病机制
Lancet Infect Dis. 2004 Aug;4(8):487-98. doi: 10.1016/S1473-3099(04)01103-X.
10
Animal models for filovirus infections.动物模型在丝状病毒感染中的应用。
Zool Res. 2018 Jan 18;39(1):15-24. doi: 10.24272/j.issn.2095-8137.2017.053.

引用本文的文献

1
Rodent adapted marburg viruses are lethal in ferrets.适应啮齿动物的马尔堡病毒对雪貂具有致死性。
Npj Viruses. 2025 Sep 8;3(1):67. doi: 10.1038/s44298-025-00147-4.
2
Identification and Structural Characterization of Viroporins from Deadly Hemorrhagic Viruses.致命出血热病毒中病毒孔蛋白的鉴定与结构表征
Viruses. 2025 Aug 14;17(8):1120. doi: 10.3390/v17081120.
3
Ebola virus VP35 NNLNS motif modulates viral RNA synthesis and MIB2-mediated signaling.埃博拉病毒VP35 NNLNS基序调节病毒RNA合成及MIB2介导的信号传导。
bioRxiv. 2025 Jul 27:2025.07.27.667045. doi: 10.1101/2025.07.27.667045.
4
The Role of Glycans in Human Immunity-A Sweet Code.聚糖在人类免疫中的作用——一个甜蜜的密码。
Molecules. 2025 Jun 20;30(13):2678. doi: 10.3390/molecules30132678.
5
Innate Immune Response to Viral Infection.对病毒感染的固有免疫反应
Adv Exp Med Biol. 2025;1476:199-224. doi: 10.1007/978-3-031-85340-1_8.
6
Bat organoids reveal antiviral responses at epithelial surfaces.蝙蝠类器官揭示上皮表面的抗病毒反应。
Nat Immunol. 2025 May 21. doi: 10.1038/s41590-025-02155-1.
7
Marburg Virus Disease: A Narrative Review.马尔堡病毒病:一篇叙述性综述。
Health Sci Rep. 2025 May 6;8(5):e70669. doi: 10.1002/hsr2.70669. eCollection 2025 May.
8
A Bivalent Bacterium-like Particles-Based Vaccine Induced Potent Immune Responses against the Sudan Virus and Ebola Virus in Mice.一种基于二价类细菌颗粒的疫苗在小鼠中诱导了针对苏丹病毒和埃博拉病毒的强效免疫反应。
Transbound Emerg Dis. 2023 Apr 24;2023:9248581. doi: 10.1155/2023/9248581. eCollection 2023.
9
A comparative analysis of the dendritic cell response upon exposure to different rabies virus strains.暴露于不同狂犬病毒株后树突状细胞反应的比较分析。
PLoS Negl Trop Dis. 2025 Apr 10;19(4):e0012994. doi: 10.1371/journal.pntd.0012994. eCollection 2025 Apr.
10
Refining early detection of Marburg Virus Disease (MVD) in Rwanda: Leveraging predictive symptom clusters to enhance case definitions.优化卢旺达马尔堡病毒病(MVD)的早期检测:利用预测性症状群来完善病例定义。
Int J Infect Dis. 2025 Jul;156:107902. doi: 10.1016/j.ijid.2025.107902. Epub 2025 Apr 3.

本文引用的文献

1
Amino Acid Residue at Position 79 of Marburg Virus VP40 Confers Interferon Antagonism in Mouse Cells.马尔堡病毒VP40第79位氨基酸残基赋予小鼠细胞中的干扰素拮抗作用。
J Infect Dis. 2015 Oct 1;212 Suppl 2(Suppl 2):S219-25. doi: 10.1093/infdis/jiv010. Epub 2015 Apr 29.
2
Human Ebola virus infection results in substantial immune activation.人类感染埃博拉病毒会导致大量免疫激活。
Proc Natl Acad Sci U S A. 2015 Apr 14;112(15):4719-24. doi: 10.1073/pnas.1502619112. Epub 2015 Mar 9.
3
Ebola virus. Two-pore channels control Ebola virus host cell entry and are drug targets for disease treatment.埃博拉病毒。双孔通道控制埃博拉病毒进入宿主细胞,是疾病治疗的药物靶点。
Science. 2015 Feb 27;347(6225):995-8. doi: 10.1126/science.1258758.
4
Oral shedding of Marburg virus in experimentally infected Egyptian fruit bats (Rousettus aegyptiacus).实验感染的埃及果蝠(埃及 Rousettus aegyptiacus)中马尔堡病毒的口腔排毒。
J Wildl Dis. 2015 Jan;51(1):113-24. doi: 10.7589/2014-08-198.
5
Deep sequencing identifies noncanonical editing of Ebola and Marburg virus RNAs in infected cells.深度测序鉴定了感染细胞中埃博拉病毒和马尔堡病毒RNA的非规范编辑。
mBio. 2014 Nov 4;5(6):e02011. doi: 10.1128/mBio.02011-14.
6
The VP40 protein of Marburg virus exhibits impaired budding and increased sensitivity to human tetherin following mouse adaptation.马尔堡病毒的VP40蛋白在适应小鼠后出芽受损,对人束缚素的敏感性增加。
J Virol. 2014 Dec;88(24):14440-50. doi: 10.1128/JVI.02069-14. Epub 2014 Oct 8.
7
Phosphatidylserine receptors: enhancers of enveloped virus entry and infection.磷脂酰丝氨酸受体:包膜病毒进入和感染的增强剂。
Virology. 2014 Nov;468-470:565-580. doi: 10.1016/j.virol.2014.09.009. Epub 2014 Sep 29.
8
Genomic surveillance elucidates Ebola virus origin and transmission during the 2014 outbreak.基因组监测解析了 2014 年埃博拉疫情期间病毒的起源和传播。
Science. 2014 Sep 12;345(6202):1369-72. doi: 10.1126/science.1259657. Epub 2014 Aug 28.
9
Molecular basis for ebolavirus VP35 suppression of human dendritic cell maturation.埃博拉病毒VP35抑制人树突状细胞成熟的分子基础
J Virol. 2014 Nov;88(21):12500-10. doi: 10.1128/JVI.02163-14. Epub 2014 Aug 20.
10
Ebola virus VP24 targets a unique NLS binding site on karyopherin alpha 5 to selectively compete with nuclear import of phosphorylated STAT1.埃博拉病毒VP24靶向核转运蛋白α5上一个独特的核定位信号结合位点,以选择性地竞争磷酸化信号转导和转录激活因子1的核输入。
Cell Host Microbe. 2014 Aug 13;16(2):187-200. doi: 10.1016/j.chom.2014.07.008.

丝状病毒发病机制与免疫逃逸:来自埃博拉病毒和马尔堡病毒的见解

Filovirus pathogenesis and immune evasion: insights from Ebola virus and Marburg virus.

作者信息

Messaoudi Ilhem, Amarasinghe Gaya K, Basler Christopher F

机构信息

School of Medicine, University of California Riverside, Riverside, California 92521, USA.

The Division of Biology &Biomedical Sciences, Washington University in St. Louis, St. Louis, Missouri 63110, USA.

出版信息

Nat Rev Microbiol. 2015 Nov;13(11):663-76. doi: 10.1038/nrmicro3524. Epub 2015 Oct 6.

DOI:10.1038/nrmicro3524
PMID:26439085
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5201123/
Abstract

Ebola viruses and Marburg viruses, members of the filovirus family, are zoonotic pathogens that cause severe disease in people, as highlighted by the latest Ebola virus epidemic in West Africa. Filovirus disease is characterized by uncontrolled virus replication and the activation of host responses that contribute to pathogenesis. Underlying these phenomena is the potent suppression of host innate antiviral responses, particularly the type I interferon response, by viral proteins, which allows high levels of viral replication. In this Review, we describe the mechanisms used by filoviruses to block host innate immunity and discuss the links between immune evasion and filovirus pathogenesis.

摘要

埃博拉病毒和马尔堡病毒属于丝状病毒科,是可导致人类严重疾病的人畜共患病原体,西非最近爆发的埃博拉病毒疫情就凸显了这一点。丝状病毒病的特征是病毒不受控制地复制以及激活导致发病机制的宿主反应。这些现象的背后是病毒蛋白对宿主先天性抗病毒反应,尤其是I型干扰素反应的有效抑制,这使得病毒能够大量复制。在本综述中,我们描述了丝状病毒用于阻断宿主先天性免疫的机制,并讨论了免疫逃逸与丝状病毒发病机制之间的联系。