• 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

辛德毕斯病毒及其复制子对BHK细胞中宿主细胞蛋白质合成及细胞致病性影响的比较

Comparison of the effects of Sindbis virus and Sindbis virus replicons on host cell protein synthesis and cytopathogenicity in BHK cells.

作者信息

Frolov I, Schlesinger S

机构信息

Department of Molecular Microbiology, Washington University School of Medicine, St. Louis, Missouri 63110-1093.

出版信息

J Virol. 1994 Mar;68(3):1721-7. doi: 10.1128/JVI.68.3.1721-1727.1994.

DOI:10.1128/JVI.68.3.1721-1727.1994
PMID:8107233
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC236632/
Abstract

Infection of BHK cells by Sindbis virus leads to rapid inhibition of host cell protein synthesis and cytopathic effects (CPE). We have been studying these events to determine whether the expression of a specific viral gene is required and, in the present study, have focused our attention on the role of the structural proteins--the capsid protein and the two membrane glycoproteins. We tested a variety of Sindbis viruses and Sindbis virus replicons (virus particles containing an RNA that is self-replicating but with some or all of the viral structural protein genes deleted) for their abilities to inhibit host cell protein synthesis and cause CPE in infected BHK cells. Our results show that shutoff of host cell protein synthesis occurred in infected BHK cells when no viral structural proteins were synthesized and also under conditions in which the level of the viral subgenomic RNA was too low to be detected. These results support the conclusion that the early steps in viral gene expression are the ones required for the inhibition of host cell protein synthesis in BHK cells. In contrast, the Sindbis viruses and Sindbis virus replicons were clearly distinguished by the time at which CPE became evident. Viruses that synthesized high levels of the two membrane glycoproteins on the surface of the infected cells caused a rapid (12 to 16 h postinfection) appearance of CPE, and those that did not synthesize the glycoprotein spikes showed delayed (30 to 40 h) CPE.

摘要

辛德毕斯病毒感染BHK细胞会导致宿主细胞蛋白质合成迅速受到抑制,并产生细胞病变效应(CPE)。我们一直在研究这些事件,以确定是否需要特定病毒基因的表达,在本研究中,我们将注意力集中在结构蛋白——衣壳蛋白和两种膜糖蛋白的作用上。我们测试了多种辛德毕斯病毒和辛德毕斯病毒复制子(含有自我复制RNA但部分或全部病毒结构蛋白基因缺失的病毒颗粒)在感染BHK细胞时抑制宿主细胞蛋白质合成和引起CPE的能力。我们的结果表明,当没有合成病毒结构蛋白时,以及在病毒亚基因组RNA水平低到无法检测的条件下,感染的BHK细胞中宿主细胞蛋白质合成均会停止。这些结果支持了这样的结论,即病毒基因表达的早期步骤是BHK细胞中抑制宿主细胞蛋白质合成所必需的。相比之下,辛德毕斯病毒和辛德毕斯病毒复制子在CPE明显出现的时间上有明显区别。在感染细胞表面合成高水平两种膜糖蛋白的病毒会导致CPE迅速出现(感染后12至16小时),而那些不合成糖蛋白刺突的病毒则表现出延迟的CPE(30至40小时)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a77b/236632/b29eac37b3ff/jvirol00012-0474-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a77b/236632/dafe4aaeb122/jvirol00012-0471-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a77b/236632/746979156146/jvirol00012-0472-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a77b/236632/a0f3653beba8/jvirol00012-0473-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a77b/236632/b29eac37b3ff/jvirol00012-0474-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a77b/236632/dafe4aaeb122/jvirol00012-0471-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a77b/236632/746979156146/jvirol00012-0472-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a77b/236632/a0f3653beba8/jvirol00012-0473-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a77b/236632/b29eac37b3ff/jvirol00012-0474-a.jpg

相似文献

1
Comparison of the effects of Sindbis virus and Sindbis virus replicons on host cell protein synthesis and cytopathogenicity in BHK cells.辛德毕斯病毒及其复制子对BHK细胞中宿主细胞蛋白质合成及细胞致病性影响的比较
J Virol. 1994 Mar;68(3):1721-7. doi: 10.1128/JVI.68.3.1721-1727.1994.
2
Sindbis virus replicons and Sindbis virus: assembly of chimeras and of particles deficient in virus RNA.辛德毕斯病毒复制子与辛德毕斯病毒:嵌合体及缺乏病毒RNA的颗粒的组装
J Virol. 1997 Apr;71(4):2819-29. doi: 10.1128/JVI.71.4.2819-2829.1997.
3
Noncytopathic Sindbis virus RNA vectors for heterologous gene expression.用于异源基因表达的非细胞病变性辛德毕斯病毒RNA载体。
Proc Natl Acad Sci U S A. 1998 Oct 27;95(22):12989-94. doi: 10.1073/pnas.95.22.12989.
4
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.
5
Translation of Sindbis virus mRNA: effects of sequences downstream of the initiating codon.辛德毕斯病毒信使核糖核酸的翻译:起始密码子下游序列的影响
J Virol. 1994 Dec;68(12):8111-7. doi: 10.1128/JVI.68.12.8111-8117.1994.
6
Identification of mutations in a Sindbis virus variant able to establish persistent infection in BHK cells: the importance of a mutation in the nsP2 gene.能够在BHK细胞中建立持续感染的辛德毕斯病毒变体中突变的鉴定:nsP2基因中一个突变的重要性
Virology. 1997 Feb 3;228(1):74-83. doi: 10.1006/viro.1996.8364.
7
Translation of Sindbis virus 26S mRNA does not require intact eukariotic initiation factor 4G.辛德毕斯病毒26S信使核糖核酸的翻译不需要完整的真核生物起始因子4G。
J Mol Biol. 2006 Feb 3;355(5):942-56. doi: 10.1016/j.jmb.2005.11.024. Epub 2005 Nov 28.
8
Viral translation is coupled to transcription in Sindbis virus-infected cells.在辛德毕斯病毒感染的细胞中,病毒翻译与转录相偶联。
J Virol. 2007 Jul;81(13):7061-8. doi: 10.1128/JVI.02529-06. Epub 2007 Apr 18.
9
Replicon vectors derived from Sindbis virus and Semliki forest virus that establish persistent replication in host cells.源自辛德毕斯病毒和塞姆利基森林病毒的复制子载体,可在宿主细胞中建立持续复制。
J Virol. 2000 Oct;74(20):9802-7. doi: 10.1128/jvi.74.20.9802-9807.2000.
10
Effect of Sindbis XJ-160 virus structural proteins on BHK-21 cell.
Zhonghua Shi Yan He Lin Chuang Bing Du Xue Za Zhi. 2000 Sep;14(3):218-22.

引用本文的文献

1
Cap-independent co-expression of dsRNA-sensing and NF-κB pathway inhibitors enables controllable self-amplifying RNA expression with reduced immunotoxicity.双链RNA感应和NF-κB通路抑制剂的非帽依赖性共表达可实现可控的自我扩增RNA表达,并降低免疫毒性。
Elife. 2025 Aug 29;14:RP105978. doi: 10.7554/eLife.105978.
2
Proteomic Analysis of CHIKV-nsP3 Host Interactions in Liver Cells Identifies Novel Interacting Partners.肝细胞中基孔肯雅病毒非结构蛋白3(CHIKV-nsP3)宿主相互作用的蛋白质组学分析鉴定出新的相互作用伴侣。
Int J Mol Sci. 2025 Jul 16;26(14):6832. doi: 10.3390/ijms26146832.
3
Translational Control of Alphavirus-Host Interactions: Implications in Viral Evolution, Tropism and Antiviral Response.

本文引用的文献

1
Conversion of lytic to persistent alphavirus infection by the bcl-2 cellular oncogene.通过bcl-2细胞癌基因将溶细胞性甲病毒感染转化为持续性感染。
Nature. 1993 Feb 25;361(6414):739-42. doi: 10.1038/361739a0.
2
Sindbis virus expression vectors: packaging of RNA replicons by using defective helper RNAs.辛德毕斯病毒表达载体:利用缺陷型辅助RNA对RNA复制子进行包装。
J Virol. 1993 Nov;67(11):6439-46. doi: 10.1128/JVI.67.11.6439-6446.1993.
3
A cell line that expresses a reporter gene in response to infection by Sindbis virus: a prototype for detection of positive strand RNA viruses.
翻译:甲病毒-宿主相互作用的翻译调控:对病毒进化、嗜性和抗病毒反应的影响。
Viruses. 2024 Jan 30;16(2):205. doi: 10.3390/v16020205.
4
Alphavirus-induced transcriptional and translational shutoffs play major roles in blocking the formation of stress granules.甲病毒诱导的转录和翻译阻断在阻止应激颗粒形成中起主要作用。
J Virol. 2023 Nov 30;97(11):e0097923. doi: 10.1128/jvi.00979-23. Epub 2023 Oct 30.
5
In-Depth Characterization of the Chikungunya Virus Replication Cycle.深入剖析基孔肯雅病毒复制周期。
J Virol. 2022 Feb 9;96(3):e0173221. doi: 10.1128/JVI.01732-21. Epub 2021 Nov 17.
6
Radicicol Inhibits Chikungunya Virus Replication by Targeting Nonstructural Protein 2.根皮素通过靶向非结构蛋白 2 抑制基孔肯雅病毒复制。
Antimicrob Agents Chemother. 2021 Jun 17;65(7):e0013521. doi: 10.1128/AAC.00135-21.
7
Sindbis viral structural protein cytotoxicity on human neuroblastoma cells.辛德毕斯病毒结构蛋白对人神经母细胞瘤细胞的细胞毒性。
Pediatr Surg Int. 2020 Oct;36(10):1173-1180. doi: 10.1007/s00383-020-04719-8. Epub 2020 Jul 21.
8
The Effects of Sindbis Viral Vectors on Neuronal Function.辛德毕斯病毒载体对神经元功能的影响。
Front Cell Neurosci. 2019 Aug 8;13:362. doi: 10.3389/fncel.2019.00362. eCollection 2019.
9
Src Family Kinase Inhibitors Block Translation of Alphavirus Subgenomic mRNAs.Src 家族激酶抑制剂阻断甲病毒亚基因组 mRNAs 的翻译。
Antimicrob Agents Chemother. 2019 Mar 27;63(4). doi: 10.1128/AAC.02325-18. Print 2019 Apr.
10
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.
一种在受到辛德毕斯病毒感染时表达报告基因的细胞系:用于检测正链RNA病毒的原型。
Virology. 1994 Jan;198(1):381-4. doi: 10.1006/viro.1994.1046.
4
An in-frame insertion into the Sindbis virus 6K gene leads to defective proteolytic processing of the virus glycoproteins, a trans-dominant negative inhibition of normal virus formation, and interference in virus shut off of host-cell protein synthesis.辛德毕斯病毒6K基因的框内插入导致病毒糖蛋白的蛋白水解加工缺陷、对正常病毒形成的反式显性负抑制以及对宿主细胞蛋白质合成的病毒关闭干扰。
Virology. 1993 Mar;193(1):424-32. doi: 10.1006/viro.1993.1139.
5
Alphaviruses--vectors for the expression of heterologous genes.甲病毒——用于表达异源基因的载体。
Trends Biotechnol. 1993 Jan;11(1):18-22. doi: 10.1016/0167-7799(93)90070-P.
6
Establishment and maintenance of persistent infection by Sindbis virus in BHK cells.辛德毕斯病毒在BHK细胞中持续感染的建立与维持
J Virol. 1980 Jan;33(1):463-74. doi: 10.1128/JVI.33.1.463-474.1980.
7
Initiation of protein synthesis in neuroblastoma cells infected by Semliki Forest Virus. A decreased requirement of late viral mRNA for eIF-4B and cap binding protein.辛德毕斯病毒感染的神经母细胞瘤细胞中蛋白质合成的起始。晚期病毒mRNA对真核生物翻译起始因子4B和帽结合蛋白的需求降低。
FEBS Lett. 1981 Jun 29;129(1):62-6. doi: 10.1016/0014-5793(81)80756-9.
8
Shutoff of neuroblastoma cell protein synthesis by Semliki Forest virus: loss of ability of crude initiation factors to recognize early Semliki Forest virus and host mRNA's.辛德毕斯病毒对神经母细胞瘤细胞蛋白质合成的阻断:粗制起始因子识别早期辛德毕斯病毒和宿主信使核糖核酸能力的丧失。
J Virol. 1981 May;38(2):728-36. doi: 10.1128/JVI.38.2.728-736.1981.
9
Infection of neuroblastoma cells by Semliki Forest virus. The interference of viral capsid protein with the binding of host messenger RNAs into initiation complexes is the cause of the shut-off of host protein synthesis.塞姆利基森林病毒对神经母细胞瘤细胞的感染。病毒衣壳蛋白干扰宿主信使核糖核酸与起始复合物的结合是宿主蛋白质合成停止的原因。
Eur J Biochem. 1984 Feb 1;138(3):473-8. doi: 10.1111/j.1432-1033.1984.tb07940.x.
10
Alterations in monovalent cation transport in Sindbis virus-infected chick cells.
Virology. 1984 Jan 15;132(1):118-30. doi: 10.1016/0042-6822(84)90096-5.