• 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

基孔肯雅热病毒的分子病毒学

Molecular Virology of Chikungunya Virus.

机构信息

Department of Microbiology, University of Alabama at Birmingham, 1720 2nd Ave South, BBRB373/Box 3, 35294-2170, Birmingham, AL, USA.

出版信息

Curr Top Microbiol Immunol. 2022;435:1-31. doi: 10.1007/82_2018_146.

DOI:10.1007/82_2018_146
PMID:30599050
Abstract

Chikungunya virus (CHIKV) was discovered more than six decades ago, but has remained poorly investigated. However, after a recent outbreak of CHIK fever in both hemispheres and viral adaptation to new species of mosquitoes, it has attracted a lot of attention. The currently available experimental data suggest that molecular mechanisms of CHIKV replication in vertebrate and mosquito cells are similar to those of other New and Old World alphaviruses. However, this virus exhibits a number of unique characteristics that distinguish it from the other, better studied members of the alphavirus genus. This review is an attempt to summarize the data accumulated thus far regarding the molecular mechanisms of alphavirus RNA replication and interaction with host cells. Emphasis was placed on demonstrating the distinct features of CHIKV in utilizing host factors to build replication complexes and modify the intracellular environment for efficient viral replication and inhibition of the innate immune response. The available data suggest that our knowledge about alphavirus replication contains numerous gaps that potentially hamper the development of new therapeutic means against CHIKV and other pathogenic alphaviruses.

摘要

基孔肯雅病毒(CHIKV)在六十年前被发现,但一直研究不足。然而,最近在两个半球爆发了基孔肯雅热,病毒也适应了新的蚊子物种,因此引起了广泛关注。目前的实验数据表明,CHIKV 在脊椎动物和蚊子细胞中的复制的分子机制与其他新、旧世界的甲病毒相似。然而,该病毒表现出许多独特的特征,使其与其他研究更为深入的甲病毒属成员区分开来。本文综述试图总结迄今为止积累的有关甲病毒 RNA 复制和与宿主细胞相互作用的分子机制的相关数据。重点在于展示 CHIKV 在利用宿主因子构建复制复合物和修饰细胞内环境以实现高效病毒复制和抑制固有免疫反应方面的独特特征。现有数据表明,我们对甲病毒复制的认识存在许多空白,这可能会阻碍针对 CHIKV 和其他致病性甲病毒的新治疗方法的开发。

相似文献

1
Molecular Virology of Chikungunya Virus.基孔肯雅热病毒的分子病毒学
Curr Top Microbiol Immunol. 2022;435:1-31. doi: 10.1007/82_2018_146.
2
Novel Mutations in nsP2 Abolish Chikungunya Virus-Induced Transcriptional Shutoff and Make the Virus Less Cytopathic without Affecting Its Replication Rates.新型 nsP2 突变消除了基孔肯雅病毒诱导的转录关闭,并降低了病毒的细胞病变效应而不影响其复制率。
J Virol. 2019 Feb 5;93(4). doi: 10.1128/JVI.02062-18. Print 2019 Feb 15.
3
Multiple Host Factors Interact with the Hypervariable Domain of Chikungunya Virus nsP3 and Determine Viral Replication in Cell-Specific Mode.多种宿主因素与基孔肯雅病毒 nsP3 的高变区相互作用,并以细胞特异性模式决定病毒复制。
J Virol. 2018 Jul 31;92(16). doi: 10.1128/JVI.00838-18. Print 2018 Aug 15.
4
NAP1L1 and NAP1L4 Binding to Hypervariable Domain of Chikungunya Virus nsP3 Protein Is Bivalent and Requires Phosphorylation.NAP1L1 和 NAP1L4 与基孔肯雅病毒 nsP3 蛋白的高变区结合具有双重性,需要磷酸化。
J Virol. 2021 Jul 26;95(16):e0083621. doi: 10.1128/JVI.00836-21.
5
Antagonism of the Sodium-Potassium ATPase Impairs Chikungunya Virus Infection.钠钾ATP酶的拮抗作用会损害基孔肯雅病毒感染。
mBio. 2016 May 24;7(3):e00693-16. doi: 10.1128/mBio.00693-16.
6
Conserved motifs in the hypervariable domain of chikungunya virus nsP3 required for transmission by Aedes aegypti mosquitoes.基孔肯雅病毒 nsP3 高变区中用于埃及伊蚊传播所必需的保守基序。
PLoS Negl Trop Dis. 2018 Nov 9;12(11):e0006958. doi: 10.1371/journal.pntd.0006958. eCollection 2018 Nov.
7
Structural and phenotypic analysis of Chikungunya virus RNA replication elements.结构和表型分析基孔肯雅病毒 RNA 复制元件。
Nucleic Acids Res. 2019 Sep 26;47(17):9296-9312. doi: 10.1093/nar/gkz640.
8
The Tetraspanin CD81 Is a Host Factor for Chikungunya Virus Replication.四跨膜蛋白 CD81 是基孔肯雅病毒复制的宿主因子。
mBio. 2022 Jun 28;13(3):e0073122. doi: 10.1128/mbio.00731-22. Epub 2022 May 25.
9
Chikungunya virus requires cellular chloride channels for efficient genome replication.基孔肯雅病毒需要细胞氯离子通道才能有效地进行基因组复制。
PLoS Negl Trop Dis. 2019 Sep 4;13(9):e0007703. doi: 10.1371/journal.pntd.0007703. eCollection 2019 Sep.
10
Disruption of the Opal Stop Codon Attenuates Chikungunya Virus-Induced Arthritis and Pathology.终止密码子通读突变可减轻基孔肯雅病毒诱导的关节炎和病理损伤。
mBio. 2017 Nov 14;8(6):e01456-17. doi: 10.1128/mBio.01456-17.

引用本文的文献

1
How Can Plant-Derived Natural Products and Plant Biotechnology Help Against Emerging Viruses?植物源天然产物和植物生物技术如何助力对抗新出现的病毒?
Int J Mol Sci. 2025 Jul 22;26(15):7046. doi: 10.3390/ijms26157046.
2
Chikungunya Replication and Infection Is Dependent upon and Alters Cellular Hexosylceramide Levels in Vero Cells.基孔肯雅病毒的复制和感染依赖于并改变了非洲绿猴肾细胞中的神经酰胺水平。
Viruses. 2025 Mar 31;17(4):509. doi: 10.3390/v17040509.
3
Withaferin A inhibits Chikungunya virus nsP2 protease and shows antiviral activity in the cell culture and mouse model of virus infection.

本文引用的文献

1
Sindbis Virus Infection Causes Cell Death by nsP2-Induced Transcriptional Shutoff or by nsP3-Dependent Translational Shutoff.辛德毕斯病毒感染通过 nsP2 诱导的转录关闭或通过 nsP3 依赖性翻译关闭引起细胞死亡。
J Virol. 2018 Nov 12;92(23). doi: 10.1128/JVI.01388-18. Print 2018 Dec 1.
2
Identification of Interactions between Sindbis Virus Capsid Protein and Cytoplasmic vRNA as Novel Virulence Determinants.辛德毕斯病毒衣壳蛋白与细胞质病毒核糖核酸之间相互作用的鉴定作为新的毒力决定因素
PLoS Pathog. 2017 Jun 29;13(6):e1006473. doi: 10.1371/journal.ppat.1006473. eCollection 2017 Jun.
3
The conserved macrodomains of the non-structural proteins of Chikungunya virus and other pathogenic positive strand RNA viruses function as mono-ADP-ribosylhydrolases.
睡茄内酯A抑制基孔肯雅病毒nsP2蛋白酶,并在病毒感染的细胞培养和小鼠模型中显示出抗病毒活性。
PLoS Pathog. 2024 Dec 30;20(12):e1012816. doi: 10.1371/journal.ppat.1012816. eCollection 2024 Dec.
4
Pathogenicity and virulence of chikungunya virus.基孔肯雅病毒的致病性和毒力。
Virulence. 2024 Dec;15(1):2396484. doi: 10.1080/21505594.2024.2396484. Epub 2024 Sep 1.
5
Advances in the Development of Non-Structural Protein 1 (NsP1) Inhibitors for the Treatment of Chikungunya Virus Infection.非结构蛋白 1(NsP1)抑制剂治疗基孔肯雅热病毒感染的研究进展。
Mini Rev Med Chem. 2024;24(22):1972-1982. doi: 10.2174/0113895575301735240607055839.
6
4'-Fluorouridine inhibits alphavirus replication and infection and .4'-氟尿苷抑制甲病毒复制和感染。
mBio. 2024 Jun 12;15(6):e0042024. doi: 10.1128/mbio.00420-24. Epub 2024 May 3.
7
Molecular characterization of Chikungunya virus recovered from patients in the Maranhão state, Brazil.从巴西马拉尼昂州患者中分离出的基孔肯雅病毒的分子特征。
Mol Biol Rep. 2024 Mar 1;51(1):375. doi: 10.1007/s11033-024-09252-8.
8
Chikungunya fever.基孔肯雅热。
Nat Rev Dis Primers. 2023 Apr 6;9(1):17. doi: 10.1038/s41572-023-00429-2.
9
Self-Amplifying RNA Vaccine Candidates: Alternative Platforms for mRNA Vaccine Development.自我扩增RNA疫苗候选物:mRNA疫苗开发的替代平台
Pathogens. 2023 Jan 13;12(1):138. doi: 10.3390/pathogens12010138.
10
Molecular architecture of the Chikungunya virus replication complex.基孔肯雅病毒复制复合体的分子结构
Sci Adv. 2022 Dec 2;8(48):eadd2536. doi: 10.1126/sciadv.add2536. Epub 2022 Nov 30.
基孔肯雅病毒和其他致病正链 RNA 病毒的非结构蛋白的保守宏结构域作为单 ADP-核糖基水解酶发挥作用。
Sci Rep. 2017 Feb 2;7:41746. doi: 10.1038/srep41746.
4
Molecular Virologic and Clinical Characteristics of a Chikungunya Fever Outbreak in La Romana, Dominican Republic, 2014.2014年多米尼加共和国拉罗马纳基孔肯雅热疫情的分子病毒学和临床特征
PLoS Negl Trop Dis. 2016 Dec 28;10(12):e0005189. doi: 10.1371/journal.pntd.0005189. eCollection 2016 Dec.
5
Chikungunya virus infectivity, RNA replication and non-structural polyprotein processing depend on the nsP2 protease's active site cysteine residue.基孔肯雅病毒的感染性、RNA 复制和非结构多蛋白加工依赖于 nsP2 蛋白酶的活性位点半胱氨酸残基。
Sci Rep. 2016 Nov 15;6:37124. doi: 10.1038/srep37124.
6
New World and Old World Alphaviruses Have Evolved to Exploit Different Components of Stress Granules, FXR and G3BP Proteins, for Assembly of Viral Replication Complexes.新大陆和旧大陆甲病毒已经进化到利用应激颗粒的不同成分,即FXR和G3BP蛋白,来组装病毒复制复合体。
PLoS Pathog. 2016 Aug 10;12(8):e1005810. doi: 10.1371/journal.ppat.1005810. eCollection 2016 Aug.
7
Structural Basis of the High Affinity Interaction between the Alphavirus Nonstructural Protein-3 (nsP3) and the SH3 Domain of Amphiphysin-2.甲病毒非结构蛋白-3(nsP3)与发动蛋白-2的SH3结构域之间高亲和力相互作用的结构基础
J Biol Chem. 2016 Jul 29;291(31):16307-17. doi: 10.1074/jbc.M116.732412. Epub 2016 Jun 6.
8
The Chikungunya virus: An emerging US pathogen.基孔肯雅病毒:一种在美国新出现的病原体。
World J Emerg Med. 2016;7(1):65-7. doi: 10.5847/wjem.j.1920-8642.2016.01.012.
9
Macrodomains: Structure, Function, Evolution, and Catalytic Activities.巨域:结构、功能、进化和催化活性。
Annu Rev Biochem. 2016 Jun 2;85:431-54. doi: 10.1146/annurev-biochem-060815-014935. Epub 2016 Jan 29.
10
Both RIG-I and MDA5 detect alphavirus replication in concentration-dependent mode.维甲酸诱导基因I(RIG-I)和黑色素瘤分化相关基因5(MDA5)均以浓度依赖模式检测甲病毒复制。
Virology. 2016 Jan;487:230-41. doi: 10.1016/j.virol.2015.09.023. Epub 2015 Nov 6.