• 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

严重急性呼吸综合征:从其他冠状病毒中吸取的教训。

SARS: lessons learned from other coronaviruses.

作者信息

Navas-Martin Sonia, Weiss Susan R

机构信息

Department of Microbiology, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania 19104-6076, USA.

出版信息

Viral Immunol. 2003;16(4):461-74. doi: 10.1089/088282403771926292.

DOI:10.1089/088282403771926292
PMID:14733734
Abstract

The identification of a new coronavirus as the etiological agent of severe acute respiratory syndrome (SARS) has evoked much new interest in the molecular biology and pathogenesis of coronaviruses. This review summarizes present knowledge on coronavirus molecular biology and pathogenesis with particular emphasis on mouse hepatitis virus (MHV). MHV, a member of coronavirus group 2, is a natural pathogen of the mouse; MHV infection of the mouse is considered one of the best models for the study of demyelinating disease, such as multiple sclerosis, in humans. As a result of the SARS epidemic, coronaviruses can now be considered as emerging pathogens. Future research on SARS needs to be based on all the knowledge that coronavirologists have generated over more than 30 years of research.

摘要

一种新型冠状病毒被确认为严重急性呼吸综合征(SARS)的病原体,这引发了人们对冠状病毒分子生物学和发病机制的新兴趣。本综述总结了目前关于冠状病毒分子生物学和发病机制的知识,特别强调了小鼠肝炎病毒(MHV)。MHV是冠状病毒第2组的成员,是小鼠的天然病原体;小鼠感染MHV被认为是研究人类脱髓鞘疾病(如多发性硬化症)的最佳模型之一。由于SARS疫情,冠状病毒现在可被视为新兴病原体。未来对SARS的研究需要基于冠状病毒学家在30多年研究中积累的所有知识。

相似文献

1
SARS: lessons learned from other coronaviruses.严重急性呼吸综合征:从其他冠状病毒中吸取的教训。
Viral Immunol. 2003;16(4):461-74. doi: 10.1089/088282403771926292.
2
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.
3
Of Mice and Men: The Coronavirus MHV and Mouse Models as a Translational Approach to Understand SARS-CoV-2.《老鼠和男人:冠状病毒 MHV 及其小鼠模型作为一种转化方法来理解 SARS-CoV-2》。
Viruses. 2020 Aug 12;12(8):880. doi: 10.3390/v12080880.
4
Coronavirus pathogenesis.冠状病毒发病机制。
Adv Virus Res. 2011;81:85-164. doi: 10.1016/B978-0-12-385885-6.00009-2.
5
[Cell entry mechanism of coronaviruses: implication in their pathogenesis].[冠状病毒的细胞进入机制:对其发病机制的影响]
Uirusu. 2006 Dec;56(2):165-71. doi: 10.2222/jsv.56.165.
6
Coronavirus nsp10/nsp16 Methyltransferase Can Be Targeted by nsp10-Derived Peptide In Vitro and In Vivo To Reduce Replication and Pathogenesis.冠状病毒nsp10/nsp16甲基转移酶可在体外和体内被源自nsp10的肽靶向,以减少复制和发病机制。
J Virol. 2015 Aug;89(16):8416-27. doi: 10.1128/JVI.00948-15. Epub 2015 Jun 3.
7
A SARS-CoV-specific protein enhances virulence of an attenuated strain of mouse hepatitis virus.一种SARS-CoV特异性蛋白增强了小鼠肝炎病毒减毒株的毒力。
Adv Exp Med Biol. 2006;581:493-8. doi: 10.1007/978-0-387-33012-9_87.
8
Animal coronaviruses: what can they teach us about the severe acute respiratory syndrome?动物冠状病毒:它们能让我们对严重急性呼吸综合征有哪些了解?
Rev Sci Tech. 2004 Aug;23(2):643-60. doi: 10.20506/rst.23.2.1513.
9
A severe acute respiratory syndrome-associated coronavirus-specific protein enhances virulence of an attenuated murine coronavirus.一种严重急性呼吸综合征相关冠状病毒特异性蛋白增强了减毒鼠冠状病毒的毒力。
J Virol. 2005 Sep;79(17):11335-42. doi: 10.1128/JVI.79.17.11335-11342.2005.
10
Epidemiology, Genetic Recombination, and Pathogenesis of Coronaviruses.冠状病毒的流行病学、基因重组与发病机制
Trends Microbiol. 2016 Jun;24(6):490-502. doi: 10.1016/j.tim.2016.03.003. Epub 2016 Mar 21.

引用本文的文献

1
Identification of promising SARS-CoV-2 main protease inhibitor through molecular docking, dynamics simulation, and ADMET analysis.通过分子对接、动力学模拟和ADMET分析鉴定有前景的新型冠状病毒主要蛋白酶抑制剂。
Sci Rep. 2025 Jan 22;15(1):2830. doi: 10.1038/s41598-025-86016-9.
2
Teicoplanin derivatives block spike protein mediated viral entry as pan-SARS-CoV-2 inhibitors.替考拉宁衍生物可阻断刺突蛋白介导的病毒进入,作为泛 SARS-CoV-2 抑制剂。
Biomed Pharmacother. 2023 Feb;158:114213. doi: 10.1016/j.biopha.2023.114213. Epub 2023 Jan 3.
3
Design and optimization of a subunit vaccine targeting COVID-19 molecular shreds using an immunoinformatics framework.
使用免疫信息学框架设计和优化针对新冠病毒分子片段的亚单位疫苗。
RSC Adv. 2020 Sep 30;10(59):35856-35872. doi: 10.1039/d0ra06849g. eCollection 2020 Sep 28.
4
Dentistry pathways of coronaviruses transmission: a review.冠状病毒的牙科传播途径:综述
Virusdisease. 2021 Dec;32(4):616-624. doi: 10.1007/s13337-021-00707-1. Epub 2021 Jul 26.
5
Genetic Characterisation and Comparison of Three Human Coronaviruses (HKU1, OC43, 229E) from Patients and Bovine Coronavirus (BCoV) from Cattle with Respiratory Disease in Slovenia.斯洛文尼亚呼吸道疾病患者体内的三种人类冠状病毒(HKU1、OC43、229E)和牛冠状病毒(BCoV)的遗传特征与比较。
Viruses. 2021 Apr 15;13(4):676. doi: 10.3390/v13040676.
6
The history of the emergence and transmission of human coronaviruses.人类冠状病毒的出现和传播历史。
Onderstepoort J Vet Res. 2021 Feb 10;88(1):e1-e8. doi: 10.4102/ojvr.v88i1.1872.
7
Overview of the current promising approaches for the development of an effective severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) vaccine.当前有希望开发有效严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)疫苗的方法概述。
Int Immunopharmacol. 2020 Nov;88:106928. doi: 10.1016/j.intimp.2020.106928. Epub 2020 Aug 24.
8
An insight into the epitope-based peptide vaccine design strategy and studies against COVID-19.基于表位的肽疫苗设计策略及抗2019冠状病毒病研究洞察
Turk J Biol. 2020 Jun 21;44(3):215-227. doi: 10.3906/biy-2006-1. eCollection 2020.
9
Synanthropic rodents as virus reservoirs and transmitters.作为病毒储存库和传播媒介的栖生啮齿动物。
Rev Soc Bras Med Trop. 2020 Feb 7;53:e20190486. doi: 10.1590/0037-8682-0486-2019. eCollection 2020.
10
Lineage A Betacoronavirus NS2 Proteins and the Homologous Torovirus Berne pp1a Carboxy-Terminal Domain Are Phosphodiesterases That Antagonize Activation of RNase L.A 型β冠状病毒 NS2 蛋白及同源的伯尔尼环曲病毒 pp1a 羧基末端结构域是拮抗 RNase L 激活的磷酸二酯酶。
J Virol. 2017 Feb 14;91(5). doi: 10.1128/JVI.02201-16. Print 2017 Mar 1.