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

生物 转录组 细胞凋亡 基因 先天免疫系统 细胞生物学 病毒 免疫系统 遗传学 黄病毒 基因表达 病毒学
作者
Yuhong Pan,Anchun Cheng,Xingcui Zhang,Mingshu Wang,Shun Chen,Dekang Zhu,Mafeng Liu,Xinxin Zhao,Qiao Yang,Ying Wu,Juan Huang,Shaqiu Zhang,Sai Mao,Xumin Ou,Qun Gao,Yanling Yu,Yunya Liu,Ling Zhang,Zhongqiong Yin,Bo Jing
出处
期刊:Aging [Impact Journals LLC]
卷期号:12 (17): 17503-17527 被引量:18
标识
DOI:10.18632/aging.103759
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.
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