Suppr超能文献

转录分析揭示了猪流行性腹泻病毒(PEDV)感染IPEC-J2细胞期间RAD51的抑制以及同源重组途径的破坏。

Transcriptional analysis reveals the suppression of RAD51 and disruption of the homologous recombination pathway during PEDV infection in IPEC-J2 cells.

作者信息

Sun Li, Cao Changfu, Yang Jianbo, Jin Jian

机构信息

School of Animal Husbandry and Veterinary Medicine, Jiangsu Vocational College of Agriculture and Forestry, Jurong, Jiangsu, 212400, China.

College of Animal Science and Technology, Nanjing Agricultural University, Nanjing, Jiangsu, 210095, China.

出版信息

Virol J. 2024 Dec 28;21(1):337. doi: 10.1186/s12985-024-02611-8.

Abstract

PEDV is a highly contagious enteric pathogen that can cause severe diarrhea and death in neonatal pigs. Despite extensive research, the molecular mechanisms of host's response to PEDV infection remain unclear. In this study, differentially expressed genes (DEGs), time-specific coexpression modules, and key regulatory genes associated with PEDV infection were identified. The analysis revealed 2,275, 1,492, and 3,409 DEGs in infected vs. mock-treated pigs at 12 h, 24 h, and 48 h, respectively. Time series analysis revealed that the upregulated genes were involved mainly in antiviral pathways such as the viral defense response and the regulation of immune system processes. Protein-protein interaction network analysis identified the top 20 core genes in the interaction network, which included six upregulated genes (TFRC, SUOX, RMI1, CD74, IFIH1, and CD86) and 14 downregulated genes (FOS, CDC6, CDCA3, PIK3R2, TUFM, VARS, ASF1B, POLD1, MCM8, POLA1, CDC45, BCS1L, RAD51, and RPA2). In addition, GSEA enrichment analysis revealed that pathways such as DNA replication and homologous recombination involving RAD51, CDC6, and RPA2 were significantly inhibited during viral infection. Our findings not only reveal dynamic changes in the transcriptome profile of PEDV-infected IPEC-J2 cells but also provide novel insights into the mechanism of PEDV infection of the host.

摘要

猪流行性腹泻病毒(PEDV)是一种高度传染性的肠道病原体,可导致新生仔猪严重腹泻和死亡。尽管进行了广泛研究,但宿主对PEDV感染的反应的分子机制仍不清楚。在本研究中,鉴定了与PEDV感染相关的差异表达基因(DEG)、时间特异性共表达模块和关键调控基因。分析显示,在感染组与 mock 处理组的猪中,分别在 12 小时、24 小时和 48 小时时检测到 2275 个、1492 个和 3409 个 DEG。时间序列分析表明,上调基因主要参与抗病毒途径,如病毒防御反应和免疫系统过程的调节。蛋白质-蛋白质相互作用网络分析确定了相互作用网络中的前 20 个核心基因,其中包括 6 个上调基因(TFRC、SUOX、RMI1、CD74、IFI1H 和 CD86)和 14 个下调基因(FOS、CDC6、CDCA3、PIK3R2、TUFM、VARS、ASF1B、POLD1、MCM8、POLA1、CDC45、BCS1L、RAD51 和 RPA2)。此外,基因集富集分析(GSEA)显示,在病毒感染期间,涉及 RAD51、CDC6 和 RPA2 的 DNA 复制和同源重组等途径受到显著抑制。我们的研究结果不仅揭示了PEDV感染的 IPEC-J2 细胞转录组谱的动态变化,还为PEDV感染宿主的机制提供了新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f711/11681661/a90226438244/12985_2024_2611_Fig1_HTML.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验