• 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

H3N2 和 H5N1 犬流感病毒感染的 MDCK 细胞全转录组 RNA 表达的比较分析。

Comparative Analysis of Whole-Transcriptome RNA Expression in MDCK Cells Infected With the H3N2 and H5N1 Canine Influenza Viruses.

机构信息

College of Veterinary Medicine, South China Agricultural University, Guangzhou, China.

Guangdong Provincial Key Laboratory of Prevention and Control for Severe Clinical Animal Diseases, Guangzhou, China.

出版信息

Front Cell Infect Microbiol. 2019 Mar 26;9:76. doi: 10.3389/fcimb.2019.00076. eCollection 2019.

DOI:10.3389/fcimb.2019.00076
PMID:30972307
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6443845/
Abstract

This study aimed to detect changes in the complete transcriptome of MDCK cells after infection with the H5N1 and H3N2 canine influenza viruses using high-throughput sequencing, search for differentially expressed RNAs in the transcriptome of MDCK cells infected with H5N1 and H3N2 using comparative analysis, and explain the differences in the pathogenicity of H5N1 and H3N2 at the transcriptome level. Based on the results of our comparative analysis, significantly different levels of expression were found for 2,464 mRNAs, 16 miRNAs, 181 lncRNAs, and 262 circRNAs in the H3N2 infection group and 448 mRNAs, 12 miRNAs, 77 lncRNAs, and 189 circRNAs in the H5N1 infection group. Potential functions were predicted by performing Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) analyses of the target genes of miRNAs, lncRNAs and circRNAs, and the ncRNA-mRNA regulatory network was constructed based on differentially expressed RNAs. A greater number of pathways regulating immune metabolism were altered in the H3N2 infection group than in the H5N1 infection group, which may be one reason why the H3N2 virus is less pathogenic than is the H5N1 virus. This study provides detailed data on the production of ncRNAs during infection of MDCK cells by the canine influenza viruses H3N2 and H5N1, analyzed differences in the total transcriptomes between H3N2- and H5N1-infected MDCK cells, and explained these differences with regard to the pathogenicity of H3N2 and H5N1 at the transcriptional level.

摘要

本研究旨在通过高通量测序检测 H5N1 和 H3N2 犬流感病毒感染 MDCK 细胞后全转录组的变化,通过比较分析寻找 H5N1 和 H3N2 感染 MDCK 细胞中转录组中差异表达的 RNA,并从转录组水平解释 H5N1 和 H3N2 致病性的差异。基于我们的比较分析结果,在 H3N2 感染组中发现 2464 个 mRNAs、16 个 miRNAs、181 个 lncRNAs 和 262 个 circRNAs 的表达水平存在显著差异,在 H5N1 感染组中发现 448 个 mRNAs、12 个 miRNAs、77 个 lncRNAs 和 189 个 circRNAs 的表达水平存在显著差异。通过对 miRNA、lncRNA 和 circRNA 的靶基因进行基因本体(GO)和京都基因与基因组百科全书(KEGG)分析,预测了它们的潜在功能,并基于差异表达的 RNA 构建了 ncRNA-mRNA 调控网络。在 H3N2 感染组中,调节免疫代谢的通路比 H5N1 感染组发生了更多的改变,这可能是 H3N2 病毒比 H5N1 病毒致病性低的原因之一。本研究提供了犬流感病毒 H3N2 和 H5N1 感染 MDCK 细胞时 ncRNA 产生的详细数据,分析了 H3N2 和 H5N1 感染的 MDCK 细胞之间总转录组的差异,并从转录水平解释了 H3N2 和 H5N1 致病性的这些差异。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/49dd/6443845/9271326226a8/fcimb-09-00076-g0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/49dd/6443845/fba7fbb03834/fcimb-09-00076-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/49dd/6443845/54485304cd84/fcimb-09-00076-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/49dd/6443845/93e20215d089/fcimb-09-00076-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/49dd/6443845/c1f535d89a57/fcimb-09-00076-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/49dd/6443845/eb5e3a002dde/fcimb-09-00076-g0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/49dd/6443845/49f7370018e9/fcimb-09-00076-g0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/49dd/6443845/9271326226a8/fcimb-09-00076-g0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/49dd/6443845/fba7fbb03834/fcimb-09-00076-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/49dd/6443845/54485304cd84/fcimb-09-00076-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/49dd/6443845/93e20215d089/fcimb-09-00076-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/49dd/6443845/c1f535d89a57/fcimb-09-00076-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/49dd/6443845/eb5e3a002dde/fcimb-09-00076-g0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/49dd/6443845/49f7370018e9/fcimb-09-00076-g0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/49dd/6443845/9271326226a8/fcimb-09-00076-g0007.jpg

相似文献

1
Comparative Analysis of Whole-Transcriptome RNA Expression in MDCK Cells Infected With the H3N2 and H5N1 Canine Influenza Viruses.H3N2 和 H5N1 犬流感病毒感染的 MDCK 细胞全转录组 RNA 表达的比较分析。
Front Cell Infect Microbiol. 2019 Mar 26;9:76. doi: 10.3389/fcimb.2019.00076. eCollection 2019.
2
Comparative analysis of MicroRNA expression in dog lungs infected with the H3N2 and H5N1 canine influenza viruses.比较感染 H3N2 和 H5N1 犬流感病毒的犬肺组织中 MicroRNA 表达的差异分析。
Microb Pathog. 2018 Aug;121:252-261. doi: 10.1016/j.micpath.2018.05.015. Epub 2018 May 14.
3
Higher titers of some H5N1 and recent human H1N1 and H3N2 influenza viruses in Mv1 Lu vs. MDCK cells.Mv1 Lu 细胞中某些 H5N1 以及最近的人源 H1N1 和 H3N2 流感病毒的滴度更高。
Virol J. 2011 Feb 11;8:66. doi: 10.1186/1743-422X-8-66.
4
Differential responses of innate immunity triggered by different subtypes of influenza a viruses in human and avian hosts.甲型流感病毒不同亚型在人类和禽类宿主中引发的先天免疫差异反应。
BMC Med Genomics. 2017 Dec 21;10(Suppl 4):70. doi: 10.1186/s12920-017-0304-z.
5
Analysis of Expression Profiles of Long Noncoding RNAs and mRNAs in A549 Cells Infected with H3N2 Swine Influenza Virus by RNA Sequencing.基于 RNA 测序的 H3N2 猪流感病毒感染 A549 细胞后长链非编码 RNA 和 mRNAs 表达谱分析。
Virol Sin. 2020 Apr;35(2):171-180. doi: 10.1007/s12250-019-00170-9. Epub 2019 Nov 27.
6
Human microRNAs profiling in response to influenza A viruses (subtypes pH1N1, H3N2, and H5N1).甲型流感病毒(pH1N1、H3N2和H5N1亚型)感染后人类微小RNA谱分析
Exp Biol Med (Maywood). 2016 Feb;241(4):409-20. doi: 10.1177/1535370215611764. Epub 2015 Oct 29.
7
Metabolic Profiles in Madin-Darby Canine Kidney Cell Lines Infected with H3N2 Canine Influenza Viruses.感染 H3N2 犬流感病毒的 Madin-Darby 犬肾细胞系中的代谢谱。
Viral Immunol. 2020 Nov;33(9):573-584. doi: 10.1089/vim.2020.0075. Epub 2020 Oct 8.
8
Generation of a High-Growth Influenza Vaccine Strain in MDCK Cells for Vaccine Preparedness.在MDCK细胞中产生用于疫苗储备的高生长流感疫苗株。
J Microbiol Biotechnol. 2018 Jun 28;28(6):997-1006. doi: 10.4014/jmb.1712.12007.
9
Analysis of cytokine production in a newly developed canine tracheal epithelial cell line infected with H3N2 canine influenza virus.对感染H3N2犬流感病毒的新建立的犬气管上皮细胞系中细胞因子产生情况的分析。
Arch Virol. 2015 Jun;160(6):1397-405. doi: 10.1007/s00705-015-2395-1. Epub 2015 Mar 24.
10
Comparison between MDCK and MDCK-SIAT1 cell lines as preferred host for cell culture-based influenza vaccine production.比较MDCK和MDCK-SIAT1细胞系作为基于细胞培养的流感疫苗生产的首选宿主。
Biotechnol Lett. 2016 Jun;38(6):941-8. doi: 10.1007/s10529-016-2069-4. Epub 2016 Mar 5.

引用本文的文献

1
Host cellular protein RAB33B facilitates influenza viral replication and modulates M2 trafficking by enhancing autophagy.宿主细胞蛋白RAB33B通过增强自噬促进流感病毒复制并调节M2转运。
Vet Res. 2025 Jul 1;56(1):129. doi: 10.1186/s13567-025-01560-6.
2
The circRNA circVAMP3 restricts influenza A virus replication by interfering with NP and NS1 proteins.环状 RNA circVAMP3 通过干扰 NP 和 NS1 蛋白来限制甲型流感病毒的复制。
PLoS Pathog. 2023 Aug 21;19(8):e1011577. doi: 10.1371/journal.ppat.1011577. eCollection 2023 Aug.
3
RNA Sequencing Demonstrates That Circular RNA Regulates Avian Influenza Virus Replication in Human Cells.

本文引用的文献

1
Comparative pathogenesis of H3N2 canine influenza virus in beagle dogs challenged by intranasal and intratracheal inoculation.经鼻腔和气管内接种挑战的比格犬中 H3N2 犬流感病毒的比较发病机制。
Virus Res. 2018 Aug 15;255:147-153. doi: 10.1016/j.virusres.2018.05.023. Epub 2018 May 31.
2
Comparative analysis of MicroRNA expression in dog lungs infected with the H3N2 and H5N1 canine influenza viruses.比较感染 H3N2 和 H5N1 犬流感病毒的犬肺组织中 MicroRNA 表达的差异分析。
Microb Pathog. 2018 Aug;121:252-261. doi: 10.1016/j.micpath.2018.05.015. Epub 2018 May 14.
3
Genetic and evolutionary analysis of emerging H3N2 canine influenza virus.
RNA 测序表明环状 RNA 调控人流感病毒复制。
Int J Mol Sci. 2022 Aug 31;23(17):9901. doi: 10.3390/ijms23179901.
4
Transcriptomic Characterization Reveals Attributes of High Influenza Virus Productivity in MDCK Cells.转录组特征分析揭示了 MDCK 细胞中流感病毒高产量的特性。
Viruses. 2021 Nov 1;13(11):2200. doi: 10.3390/v13112200.
5
Whole Transcriptome Analysis Revealed a Stress Response to Deep Underground Environment Conditions in Chinese Hamster V79 Lung Fibroblast Cells.全转录组分析揭示了中国仓鼠V79肺成纤维细胞对深层地下环境条件的应激反应。
Front Genet. 2021 Sep 16;12:698046. doi: 10.3389/fgene.2021.698046. eCollection 2021.
6
Molecular Characteristics, Antigenicity, Pathogenicity, and Zoonotic Potential of a H3N2 Canine Influenza Virus Currently Circulating in South China.中国南方目前流行的H3N2犬流感病毒的分子特征、抗原性、致病性及人畜共患病潜力
Front Microbiol. 2021 Mar 9;12:628979. doi: 10.3389/fmicb.2021.628979. eCollection 2021.
7
Phosphoproteomics to Characterize Host Response During H3N2 Canine Influenza Virus Infection of Dog Lung.磷酸化蛋白质组学用于表征犬H3N2流感病毒感染犬肺期间的宿主反应
Front Vet Sci. 2020 Dec 3;7:585071. doi: 10.3389/fvets.2020.585071. eCollection 2020.
8
Viruses join the circular RNA world.病毒加入环状 RNA 世界。
FEBS J. 2021 Aug;288(15):4488-4502. doi: 10.1111/febs.15639. Epub 2020 Dec 9.
9
Competing endogenous RNA network profiling reveals novel host dependency factors required for MERS-CoV propagation.竞争性内源性 RNA 网络谱分析揭示了新型宿主依赖因子,这些因子是 MERS-CoV 传播所必需的。
Emerg Microbes Infect. 2020 Dec;9(1):733-746. doi: 10.1080/22221751.2020.1738277.
10
Viral Determinants in H5N1 Influenza A Virus Enable Productive Infection of HeLa Cells.H5N1 流感病毒中的病毒决定因素使 HeLa 细胞能够进行有效感染。
J Virol. 2020 Jan 31;94(4). doi: 10.1128/JVI.01410-19.
新兴 H3N2 犬流感病毒的遗传与进化分析。
Emerg Microbes Infect. 2018 Apr 25;7(1):73. doi: 10.1038/s41426-018-0079-0.
4
Integrated Lung and Tracheal mRNA-Seq and miRNA-Seq Analysis of Dogs with an Avian-Like H5N1 Canine Influenza Virus Infection.感染类禽流感H5N1犬流感病毒的犬类肺和气管mRNA测序及miRNA测序综合分析
Front Microbiol. 2018 Mar 5;9:303. doi: 10.3389/fmicb.2018.00303. eCollection 2018.
5
H5N1 influenza virus-specific miRNA-like small RNA increases cytokine production and mouse mortality via targeting poly(rC)-binding protein 2.H5N1 流感病毒特异性 miRNA 样小 RNA 通过靶向聚(rC)结合蛋白 2 增加细胞因子产生和小鼠死亡率。
Cell Res. 2018 Feb;28(2):157-171. doi: 10.1038/cr.2018.3. Epub 2018 Jan 12.
6
Assessment of Molecular, Antigenic, and Pathological Features of Canine Influenza A(H3N2) Viruses That Emerged in the United States.对在美国出现的犬甲型流感病毒(H3N2)的分子、抗原和病理学特征的评估
J Infect Dis. 2017 Sep 15;216(suppl_4):S499-S507. doi: 10.1093/infdis/jiw620.
7
Spread of Canine Influenza A(H3N2) Virus, United States.美国甲型流感病毒(H3N2)的传播。
Emerg Infect Dis. 2017 Dec;23(12):1950-1957. doi: 10.3201/eid2312.170246. Epub 2017 Dec 17.
8
Long noncoding RNAs: lincs between human health and disease.长链非编码RNA:人类健康与疾病之间的纽带
Biochem Soc Trans. 2017 Jun 15;45(3):805-812. doi: 10.1042/BST20160376.
9
MicroRNA 34a contributes to virus-mediated apoptosis through binding to its target gene Bax in influenza A virus infection.微小RNA 34a在甲型流感病毒感染中通过与靶基因Bax结合促进病毒介导的细胞凋亡。
Biomed Pharmacother. 2016 Oct;83:1464-1470. doi: 10.1016/j.biopha.2016.08.049. Epub 2016 Sep 6.
10
Influenza A Virus-Induced Expression of a GalNAc Transferase, GALNT3, via MicroRNAs Is Required for Enhanced Viral Replication.甲型流感病毒通过微小RNA诱导的N-乙酰半乳糖胺转移酶GALNT3的表达是增强病毒复制所必需的。
J Virol. 2015 Dec 4;90(4):1788-801. doi: 10.1128/JVI.02246-15. Print 2016 Feb 15.