• 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感染早期 Vero E6 细胞的转录组特征。

Transcriptional Landscape of Vero E6 Cells during Early Swine Acute Diarrhea Syndrome Coronavirus Infection.

机构信息

State Key Laboratory of Biocontrol, Life Sciences School, Sun Yat-sen University, Guangzhou 510006, China.

Guangdong Provincial Key Laboratory of Malignant Tumor Epigenetics and Gene Regulation, Sun Yat-sen University, Guangzhou 510120, China.

出版信息

Viruses. 2021 Apr 14;13(4):674. doi: 10.3390/v13040674.

DOI:10.3390/v13040674
PMID:33919952
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8070899/
Abstract

Swine acute diarrhea syndrome coronavirus (SADS-CoV) is a newly emerged and highly pathogenic virus that is associated with fatal diarrhea disease in piglets, causing significant economic losses to the pig industry. At present, the research on the pathogenicity and molecular mechanisms of host-virus interactions of SADS-CoV are limited and remain poorly understood. Here, we investigated the global gene expression profiles of SADS-CoV-infected Vero E6 cells at 12, 18, and 24 h post-infection (hpi) using the RNA-sequencing. As a result, a total of 3324 differentially expressed genes (DEG) were identified, most of which showed a down-regulated expression pattern. Functional enrichment analyses indicated that the DEGs are mainly involved in signal transduction, cellular transcription, immune and inflammatory response, and autophagy. Collectively, our results provide insights into the changes in the cellular transcriptome during early infection of SADS-CoV and may provide information for further study of molecular mechanisms.

摘要

猪急性腹泻综合征冠状病毒(SADS-CoV)是一种新出现的高致病性病毒,与仔猪致命性腹泻病有关,给养猪业造成了重大经济损失。目前,关于 SADS-CoV 的致病性和宿主-病毒相互作用的分子机制的研究有限,了解甚少。在这里,我们使用 RNA 测序技术研究了感染 SADS-CoV 的 Vero E6 细胞在感染后 12、18 和 24 小时的全基因表达谱。结果共鉴定出 3324 个差异表达基因(DEG),其中大多数呈下调表达模式。功能富集分析表明,DEGs 主要参与信号转导、细胞转录、免疫和炎症反应以及自噬。综上所述,我们的研究结果为 SADS-CoV 早期感染过程中细胞转录组的变化提供了新的见解,为进一步研究分子机制提供了信息。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8a1/8070899/a812a224dbc1/viruses-13-00674-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8a1/8070899/67fe8320e28f/viruses-13-00674-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8a1/8070899/2d3f80a5b606/viruses-13-00674-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8a1/8070899/484af0ee8136/viruses-13-00674-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8a1/8070899/b088627b5358/viruses-13-00674-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8a1/8070899/dd1a462a7592/viruses-13-00674-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8a1/8070899/2247321961eb/viruses-13-00674-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8a1/8070899/30c6aeaa6026/viruses-13-00674-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8a1/8070899/7a32f929b1be/viruses-13-00674-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8a1/8070899/a812a224dbc1/viruses-13-00674-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8a1/8070899/67fe8320e28f/viruses-13-00674-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8a1/8070899/2d3f80a5b606/viruses-13-00674-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8a1/8070899/484af0ee8136/viruses-13-00674-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8a1/8070899/b088627b5358/viruses-13-00674-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8a1/8070899/dd1a462a7592/viruses-13-00674-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8a1/8070899/2247321961eb/viruses-13-00674-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8a1/8070899/30c6aeaa6026/viruses-13-00674-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8a1/8070899/7a32f929b1be/viruses-13-00674-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8a1/8070899/a812a224dbc1/viruses-13-00674-g009.jpg

相似文献

1
Transcriptional Landscape of Vero E6 Cells during Early Swine Acute Diarrhea Syndrome Coronavirus Infection.猪急性腹泻综合征冠状病毒感染早期 Vero E6 细胞的转录组特征。
Viruses. 2021 Apr 14;13(4):674. doi: 10.3390/v13040674.
2
Swine acute diarrhea syndrome coronavirus-induced apoptosis is caspase- and cyclophilin D- dependent.猪急性腹泻综合征冠状病毒诱导的细胞凋亡依赖于半胱天冬酶和亲环素 D。
Emerg Microbes Infect. 2020 Feb 24;9(1):439-456. doi: 10.1080/22221751.2020.1722758. eCollection 2020.
3
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.
4
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.
5
Epitope mapping and cellular localization of swine acute diarrhea syndrome coronavirus nucleocapsid protein using a novel monoclonal antibody.利用新型单克隆抗体进行猪急性腹泻综合征冠状病毒核衣壳蛋白的表位作图和细胞定位。
Virus Res. 2019 Nov;273:197752. doi: 10.1016/j.virusres.2019.197752. Epub 2019 Sep 10.
6
RNA-Seq-Based Whole Transcriptome Analysis of IPEC-J2 Cells During Swine Acute Diarrhea Syndrome Coronavirus Infection.猪急性腹泻综合征冠状病毒感染期间IPEC-J2细胞基于RNA测序的全转录组分析
Front Vet Sci. 2020 Aug 13;7:492. doi: 10.3389/fvets.2020.00492. eCollection 2020.
7
Swine acute diarrhea syndrome coronavirus replication is reduced by inhibition of the extracellular signal-regulated kinase (ERK) signaling pathway.猪急性腹泻综合征冠状病毒的复制受到细胞外信号调节激酶(ERK)信号通路抑制的影响。
Virology. 2022 Jan 2;565:96-105. doi: 10.1016/j.virol.2021.10.009. Epub 2021 Oct 30.
8
Swine acute diarrhea syndrome coronavirus replication in primary human cells reveals potential susceptibility to infection.猪急性腹泻综合征冠状病毒在原代人细胞中的复制揭示了潜在的感染易感性。
Proc Natl Acad Sci U S A. 2020 Oct 27;117(43):26915-26925. doi: 10.1073/pnas.2001046117. Epub 2020 Oct 12.
9
Attenuation of a virulent swine acute diarrhea syndrome coronavirus strain via cell culture passage.通过细胞传代降低猪急性腹泻综合征冠状病毒强毒株的毒力。
Virology. 2019 Dec;538:61-70. doi: 10.1016/j.virol.2019.09.009. Epub 2019 Sep 21.
10
SADS-CoV nsp1 inhibits the STAT1 phosphorylation by promoting K11/K48-linked polyubiquitination of JAK1 and blocks the STAT1 acetylation by degrading CBP.SADS-CoV nsp1 通过促进 JAK1 的 K11/K48 连接多泛素化来抑制 STAT1 的磷酸化,并通过降解 CBP 来阻断 STAT1 的乙酰化。
J Biol Chem. 2024 Mar;300(3):105779. doi: 10.1016/j.jbc.2024.105779. Epub 2024 Feb 21.

引用本文的文献

1
The swine acute diarrhea syndrome coronavirus spike protein promotes syncytial formation via upregulation of cellular cholesterol synthesis.猪急性腹泻综合征冠状病毒刺突蛋白通过上调细胞胆固醇合成促进合胞体形成。
mBio. 2025 Jun 30:e0097625. doi: 10.1128/mbio.00976-25.
2
Swine Acute Diarrhea Syndrome Coronavirus: An Overview of Virus Structure and Virus-Host Interactions.猪急性腹泻综合征冠状病毒:病毒结构与病毒-宿主相互作用概述
Animals (Basel). 2025 Jan 9;15(2):149. doi: 10.3390/ani15020149.
3
Interaction between coronaviruses and the autophagic response.

本文引用的文献

1
Swine Acute Diarrhea Syndrome Coronavirus Nucleocapsid Protein Antagonizes Interferon- Production Blocking the Interaction Between TRAF3 and TBK1.猪急性腹泻综合征冠状病毒核衣壳蛋白拮抗干扰素产生,阻断 TRAF3 和 TBK1 的相互作用。
Front Immunol. 2021 Feb 22;12:573078. doi: 10.3389/fimmu.2021.573078. eCollection 2021.
2
Broad Cell Tropism of SADS-CoV In Vitro Implies Its Potential Cross-Species Infection Risk.SADS-CoV在体外的广泛细胞嗜性表明其具有潜在的跨物种感染风险。
Virol Sin. 2021 Jun;36(3):559-563. doi: 10.1007/s12250-020-00321-3. Epub 2020 Nov 17.
3
Swine acute diarrhea syndrome coronavirus replication in primary human cells reveals potential susceptibility to infection.
冠状病毒与自噬反应之间的相互作用。
Front Cell Infect Microbiol. 2024 Nov 22;14:1457617. doi: 10.3389/fcimb.2024.1457617. eCollection 2024.
4
Research Advances on Swine Acute Diarrhea Syndrome Coronavirus.猪急性腹泻综合征冠状病毒的研究进展
Animals (Basel). 2024 Jan 30;14(3):448. doi: 10.3390/ani14030448.
5
Interplay between swine enteric coronaviruses and host innate immune.猪肠道冠状病毒与宿主固有免疫之间的相互作用。
Front Vet Sci. 2022 Dec 22;9:1083605. doi: 10.3389/fvets.2022.1083605. eCollection 2022.
6
Swine acute diarrhea syndrome coronavirus induces autophagy to promote its replication via the Akt/mTOR pathway.猪急性腹泻综合征冠状病毒通过Akt/mTOR途径诱导自噬以促进其复制。
iScience. 2022 Nov 18;25(11):105394. doi: 10.1016/j.isci.2022.105394. Epub 2022 Oct 20.
7
Effectiveness of Booster Doses of the SARS-CoV-2 Inactivated Vaccine KCONVAC against the Mutant Strains.加强针对 SARS-CoV-2 灭活疫苗 KCONVAC 对变异株的有效性。
Viruses. 2022 Sep 12;14(9):2016. doi: 10.3390/v14092016.
8
The Effects of Swine Coronaviruses on ER Stress, Autophagy, Apoptosis, and Alterations in Cell Morphology.猪冠状病毒对内质网应激、自噬、凋亡及细胞形态改变的影响
Pathogens. 2022 Aug 19;11(8):940. doi: 10.3390/pathogens11080940.
9
Differing coronavirus genres alter shared host signaling pathways upon viral infection.不同的冠状病毒属在病毒感染时改变宿主共享的信号通路。
Sci Rep. 2022 Jun 13;12(1):9744. doi: 10.1038/s41598-022-13396-7.
10
Swine Enteric Coronavirus: Diverse Pathogen-Host Interactions.猪传染性胃肠炎病毒:不同的病原体-宿主相互作用。
Int J Mol Sci. 2022 Apr 2;23(7):3953. doi: 10.3390/ijms23073953.
猪急性腹泻综合征冠状病毒在原代人细胞中的复制揭示了潜在的感染易感性。
Proc Natl Acad Sci U S A. 2020 Oct 27;117(43):26915-26925. doi: 10.1073/pnas.2001046117. Epub 2020 Oct 12.
4
RNA-Seq-Based Whole Transcriptome Analysis of IPEC-J2 Cells During Swine Acute Diarrhea Syndrome Coronavirus Infection.猪急性腹泻综合征冠状病毒感染期间IPEC-J2细胞基于RNA测序的全转录组分析
Front Vet Sci. 2020 Aug 13;7:492. doi: 10.3389/fvets.2020.00492. eCollection 2020.
5
Structural and Biological Basis of Alphacoronavirus nsp1 Associated with Host Proliferation and Immune Evasion.结构与生物基础:甲型冠状病毒 nsp1 与宿主增殖和免疫逃避相关。
Viruses. 2020 Jul 28;12(8):812. doi: 10.3390/v12080812.
6
Dysregulation in Akt/mTOR/HIF-1 signaling identified by proteo-transcriptomics of SARS-CoV-2 infected cells.通过 SARS-CoV-2 感染细胞的蛋白质组 - 转录组学鉴定的 Akt/mTOR/HIF-1 信号通路失调。
Emerg Microbes Infect. 2020 Dec;9(1):1748-1760. doi: 10.1080/22221751.2020.1799723.
7
Nonstructural protein 6 of porcine epidemic diarrhea virus induces autophagy to promote viral replication via the PI3K/Akt/mTOR axis.猪流行性腹泻病毒非结构蛋白 6 通过 PI3K/Akt/mTOR 轴诱导自噬促进病毒复制。
Vet Microbiol. 2020 May;244:108684. doi: 10.1016/j.vetmic.2020.108684. Epub 2020 Apr 18.
8
Transcriptional landscape of SARS-CoV-2 infection dismantles pathogenic pathways activated by the virus, proposes unique sex-specific differences and predicts tailored therapeutic strategies.SARS-CoV-2 感染的转录组景观剖析了病毒激活的致病途径,提出了独特的性别特异性差异,并预测了针对性的治疗策略。
Autoimmun Rev. 2020 Jul;19(7):102571. doi: 10.1016/j.autrev.2020.102571. Epub 2020 May 3.
9
PEDV enters cells through clathrin-, caveolae-, and lipid raft-mediated endocytosis and traffics via the endo-/lysosome pathway.PEDV 通过网格蛋白、小窝蛋白和脂筏介导的内吞作用进入细胞,并通过内体/溶酶体途径运输。
Vet Res. 2020 Feb 10;51(1):10. doi: 10.1186/s13567-020-0739-7.
10
The characteristics of hDPP4 transgenic mice subjected to aerosol MERS coronavirus infection via an animal nose-only exposure device.通过动物专用鼻暴露装置经气溶胶感染中东呼吸综合征冠状病毒的人源二肽基肽酶4(hDPP4)转基因小鼠的特征。
Animal Model Exp Med. 2019 Oct 30;2(4):269-281. doi: 10.1002/ame2.12088. eCollection 2019 Dec.