• 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

猪急性腹泻综合征冠状病毒与宿主固有免疫和天然免疫的相互作用。

Interplay of swine acute diarrhoea syndrome coronavirus and the host intrinsic and innate immunity.

作者信息

Zhao Fei, Cong Xiao, Huang Xiaobo, Zheng Yi, Zhao Qin, Wen Yiping, Wu Rui, Du Senyan, Cao Sanjie, Cong Feng, Wang Yiping

机构信息

Department of Preventive Veterinary Medicine, Research Center for Swine Diseases, College of Veterinary Medicine, Sichuan Agricultural University, Chengdu, 611130, China.

Guangdong Laboratory Animals Monitoring Institute, Guangzhou, 510663, Guangdong, China.

出版信息

Vet Res. 2025 Jan 9;56(1):5. doi: 10.1186/s13567-024-01436-1.

DOI:10.1186/s13567-024-01436-1
PMID:39789633
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11720510/
Abstract

Swine acute diarrhoea syndrome coronavirus (SADS-CoV), a novel HKU2-related coronavirus of bat origin, is a newly emerged swine enteropathogenic coronavirus that causes severe diarrhoea in piglets. SADS-CoV has a broad cell tropism with the capability to infect a wide variety of cells from human and diverse animals, which implicates its ability to hold high risks of cross-species transmission. The intracellular antiviral immunity, comprised of the intrinsic and innate immunity, represents the first line of host defence against viral infection prior to the onset of adaptive immunity. To date, there are no vaccines and drugs approved to prevent or treat SADS-CoV infection. Understanding of the mutual relationship between SADS-CoV infection and host immunity is crucial for the development of novel vaccines and drugs against SADS-CoV. Here, we review recent advancements in our understanding of the interplay between SADS-CoV infection and the host intrinsic and innate immunity. The extensive and in-depth investigation on their interactive relationship will contribute to the identification of new targets for developing intervention strategies to control SADS-CoV infection.

摘要

猪急性腹泻综合征冠状病毒(SADS-CoV)是一种源自蝙蝠的新型HKU2相关冠状病毒,是一种新出现的猪肠道致病性冠状病毒,可导致仔猪严重腹泻。SADS-CoV具有广泛的细胞嗜性,能够感染来自人类和多种动物的多种细胞,这意味着它具有很高的跨物种传播风险。由固有免疫和天然免疫组成的细胞内抗病毒免疫是宿主在适应性免疫开始之前抵御病毒感染的第一道防线。迄今为止,尚无批准用于预防或治疗SADS-CoV感染的疫苗和药物。了解SADS-CoV感染与宿主免疫之间的相互关系对于开发针对SADS-CoV的新型疫苗和药物至关重要。在此,我们综述了目前对SADS-CoV感染与宿主固有免疫和天然免疫之间相互作用的最新认识进展。对它们相互作用关系的广泛而深入的研究将有助于确定开发控制SADS-CoV感染干预策略的新靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dbc2/11720510/f46ce9af03c3/13567_2024_1436_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dbc2/11720510/d88181b724c1/13567_2024_1436_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dbc2/11720510/0cba18b22dcf/13567_2024_1436_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dbc2/11720510/e14ff8069b2e/13567_2024_1436_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dbc2/11720510/f46ce9af03c3/13567_2024_1436_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dbc2/11720510/d88181b724c1/13567_2024_1436_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dbc2/11720510/0cba18b22dcf/13567_2024_1436_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dbc2/11720510/e14ff8069b2e/13567_2024_1436_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dbc2/11720510/f46ce9af03c3/13567_2024_1436_Fig4_HTML.jpg

相似文献

1
Interplay of swine acute diarrhoea syndrome coronavirus and the host intrinsic and innate immunity.猪急性腹泻综合征冠状病毒与宿主固有免疫和天然免疫的相互作用。
Vet Res. 2025 Jan 9;56(1):5. doi: 10.1186/s13567-024-01436-1.
2
Broad Cross-Species Infection of Cultured Cells by Bat HKU2-Related Swine Acute Diarrhea Syndrome Coronavirus and Identification of Its Replication in Murine Dendritic Cells Highlight Its Potential for Diverse Interspecies Transmission.蝙蝠 HKU2 相关猪急性腹泻综合征冠状病毒对培养细胞的广泛跨种感染及其在鼠树突状细胞中的复制鉴定提示其具有潜在的多种种间传播能力。
J Virol. 2019 Nov 26;93(24). doi: 10.1128/JVI.01448-19. Print 2019 Dec 15.
3
NS7a of SADS-CoV promotes viral infection via inducing apoptosis to suppress type III interferon production.SADS-CoV 的 NS7a 通过诱导细胞凋亡抑制 III 型干扰素的产生从而促进病毒感染。
J Virol. 2024 May 14;98(5):e0031724. doi: 10.1128/jvi.00317-24. Epub 2024 Apr 16.
4
Comprehensive Subcellular Localization of Swine Acute Diarrhea Syndrome Coronavirus Proteins.猪流行性腹泻病毒蛋白的全面亚细胞定位。
J Virol. 2022 Sep 14;96(17):e0077222. doi: 10.1128/jvi.00772-22. Epub 2022 Aug 16.
5
Retrospective detection and phylogenetic analysis of swine acute diarrhoea syndrome coronavirus in pigs in southern China.中国南方猪群中猪急性腹泻综合征冠状病毒的回溯性检测与系统进化分析。
Transbound Emerg Dis. 2019 Mar;66(2):687-695. doi: 10.1111/tbed.13008. Epub 2019 Jan 9.
6
Recombinant porcine interferon delta 8 inhibits swine acute diarrhoea syndrome coronavirus infection in vitro and in vivo.重组猪干扰素 delta 8 抑制猪急性腹泻综合征冠状病毒在体内外感染。
Vet Res. 2024 Jul 24;55(1):92. doi: 10.1186/s13567-024-01346-2.
7
Bat-Origin Swine Acute Diarrhea Syndrome Coronavirus Is Lethal to Neonatal Mice.猪急性腹泻综合征冠状病毒来源于蝙蝠,可致新生乳鼠死亡。
J Virol. 2023 Mar 30;97(3):e0019023. doi: 10.1128/jvi.00190-23. Epub 2023 Mar 6.
8
Identification of ZDHHC17 as a Potential Drug Target for Swine Acute Diarrhea Syndrome Coronavirus Infection.鉴定 ZDHHC17 为猪急性腹泻综合征冠状病毒感染的潜在药物靶点。
mBio. 2021 Oct 26;12(5):e0234221. doi: 10.1128/mBio.02342-21.
9
A Customized Novel Blocking ELISA for Detection of Bat-Origin Swine Acute Diarrhea Syndrome Coronavirus Infection.定制阻断 ELISA 用于检测蝙蝠源猪急性腹泻综合征冠状病毒感染。
Microbiol Spectr. 2023 Aug 17;11(4):e0393022. doi: 10.1128/spectrum.03930-22. Epub 2023 Jun 5.
10
Swine acute diarrhea syndrome coronavirus (SADS-CoV) antagonizes interferon-β production via blocking IPS-1 and RIG-I.猪急性腹泻综合征冠状病毒(SADS-CoV)通过阻断 IPS-1 和 RIG-I 来拮抗干扰素-β的产生。
Virus Res. 2020 Mar;278:197843. doi: 10.1016/j.virusres.2019.197843. Epub 2019 Dec 26.

本文引用的文献

1
Recombinant porcine interferon delta 8 inhibits swine acute diarrhoea syndrome coronavirus infection in vitro and in vivo.重组猪干扰素 delta 8 抑制猪急性腹泻综合征冠状病毒在体内外感染。
Vet Res. 2024 Jul 24;55(1):92. doi: 10.1186/s13567-024-01346-2.
2
TMPRSS13 promotes the cell entry of swine acute diarrhea syndrome coronavirus.TMPRSS13 促进猪急性腹泻综合征冠状病毒的细胞进入。
J Med Virol. 2024 Jun;96(6):e29712. doi: 10.1002/jmv.29712.
3
NS7a of SADS-CoV promotes viral infection via inducing apoptosis to suppress type III interferon production.
SADS-CoV 的 NS7a 通过诱导细胞凋亡抑制 III 型干扰素的产生从而促进病毒感染。
J Virol. 2024 May 14;98(5):e0031724. doi: 10.1128/jvi.00317-24. Epub 2024 Apr 16.
4
Physiological functions of RIG-I-like receptors.RIG-I 样受体的生理功能。
Immunity. 2024 Apr 9;57(4):731-751. doi: 10.1016/j.immuni.2024.03.003.
5
The conceptual foundations of innate immunity: Taking stock 30 years later.先天性免疫的概念基础:30 年后的回顾。
Immunity. 2024 Apr 9;57(4):613-631. doi: 10.1016/j.immuni.2024.03.007.
6
Swine acute diarrhea syndrome coronavirus Nsp1 suppresses IFN-λ1 production by degrading IRF1 via ubiquitin-proteasome pathway.猪急性腹泻综合征冠状病毒 Nsp1 通过泛素-蛋白酶体途径降解 IRF1 抑制 IFN-λ1 的产生。
Vet Res. 2024 Apr 8;55(1):45. doi: 10.1186/s13567-024-01299-6.
7
Swine acute diarrhea syndrome coronavirus nucleocapsid protein antagonizes the IFN response through inhibiting TRIM25 oligomerization and functional activation of RIG-I/TRIM25.猪急性腹泻综合征冠状病毒核衣壳蛋白通过抑制 TRIM25 寡聚化和 RIG-I/TRIM25 的功能激活来拮抗 IFN 反应。
Vet Res. 2024 Apr 8;55(1):44. doi: 10.1186/s13567-024-01303-z.
8
Establishment of replication-competent vesicular stomatitis virus recapitulating SADS-CoV entry.建立复制型水疱性口炎病毒重现 SADS-CoV 进入的过程。
J Virol. 2024 May 14;98(5):e0195723. doi: 10.1128/jvi.01957-23. Epub 2024 Apr 1.
9
Functional dissection of the spike glycoprotein S1 subunit and identification of cellular cofactors for regulation of swine acute diarrhea syndrome coronavirus entry.解析刺突糖蛋白 S1 亚基的功能,并鉴定调控猪急性腹泻综合征冠状病毒进入的细胞辅助因子。
J Virol. 2024 Apr 16;98(4):e0013924. doi: 10.1128/jvi.00139-24. Epub 2024 Mar 19.
10
Re-emergence of severe acute diarrhea syndrome coronavirus (SADS-CoV) in Henan, central China, 2023.2023 年中国中部河南省严重急性腹泻综合征冠状病毒(SADS-CoV)再现。
Vet Microbiol. 2024 May;292:110049. doi: 10.1016/j.vetmic.2024.110049. Epub 2024 Mar 15.