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Transcriptome analysis of duck embryo fibroblasts for the dynamic response to duck tembusu virus infection and dual regulation of apoptosis genes

机译:鸭胚胎成纤维细胞的转录体分析对鸭竹病病毒感染的动态响应及凋亡基因的双重调控

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摘要

Duck Tembusu virus (DTMUV) is an emerging pathogenic flavivirus that has caused enormous economic losses in Southeast Asia. However, the pathogenic mechanism and host’s responses after DTMUV infection remain poorly understood. During this study, total mRNA sequencing (RNA-Seq) analysis was used to detect the global gene expression in DEFs at various time points after DTMUV infection. We identified 326 genes altered significantly at all time points, and these genes were dynamically enriched in multifarious biological processes, including apoptosis, innate immune response, DNA replication, cell cycle arrest and DNA repair. Next, the results showed that apoptosis was induced and the proportion of apoptosis increased with time, and pro-apoptotic molecules caspases were activated. The RNA-seq data analysis further revealed that most pro-apoptosis and anti-apoptosis genes were early continually responsive, and the genes involved in both intrinsic and extrinsic apoptotic pathways were initiated. Further, the considerably enriched immune-relevant pathways were involved in apoptosis process, and protein-protein interactions (PPIs) analysis showed that IL6, STAT1, TNFAIP3, CFLAR and PTGS2 may be key regulators of DEFs apoptosis. In conclusion, this study not only contributes to understanding the underlying mechanism of DEFs infection with DTMUV, but also provides new insights into targets screening for antiviral therapy.
机译:Duck Tembusu病毒(DTMUV)是一种新兴致病性黄病毒,在东南亚导致了巨大的经济损失。然而,在DTMUV感染后,病原机制和宿主的反应仍然很清楚。在该研究期间,使用总MRNA测序(RNA-SEQ)分析来检测DTMUV感染后各个时间点的DEFS中的全局基因表达。我们鉴定了326个基因在所有时间点显着改变,这些基因在多种生物过程中动态富集,包括细胞凋亡,先天免疫应答,DNA复制,细胞周期停滞和DNA修复。接下来,结果表明诱导细胞凋亡,随时间增加凋亡的比例,并激活促凋亡分子胱天蛋白酶。 RNA-SEQ数据分析进一步揭示了大多数促细胞凋亡和抗凋亡基因持续响应,并且已经开始了内在和外部凋亡途径的涉及的基因。此外,相当富集的免疫相关途径参与凋亡过程,蛋白质 - 蛋白质相互作用(PPI)分析显示IL6,STAT1,TNFAIP3,CFLAR和PTGS2可以是DECS细胞凋亡的关键调节因子。总之,这项研究不仅有助于了解DTMUV的Defs感染的潜在机制,还为抗病毒治疗筛查提供了新的见解。

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