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Transcriptome Analysis of Epithelioma Papulosum Cyprini Cells Infected by Reovirus Isolated from Allogynogenetic Silver Crucian Carp

机译:分离自拟南芥Cru的呼肠孤病毒感染的上皮瘤细胞的转录组分析

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摘要

The present study aimed to identify differentially expressed genes (DEGs) and major signal transduction pathways that were related to the immune response of epithelioma papulosum cyprinid (EPC) cells to reoviruses isolated from allogynogenetic silver crucian carp. The study also lays a theoretical foundation for the pathogenesis and immunity of the reovirus, which is helpful to the breeding of cyprinids fish. Reovirus infected and uninfected EPC cells were analyzed by using a new-generation high-throughput sequencing technology. DEGs were identified, annotated, and classified, and the signal pathways involved in the response to reovirus infection were identified by using bioinformatics tool. The data were assembled into 92,101 contigs with an average length of 835.24 bp and an N50 value of 1432 nt. Differential expression analysis of all the genes identified 3316 DEGs at a false discovery rate (FDR) of <0.01 and a fold-change of ≥3, of which 1691 were upregulated genes, 1625 were downregulated, and about 305 were immune-related genes. Gene Ontology (GO) enrichment analysis resulted in the annotation of 3941 GO terms, including 2719 biological processes (37,810 unigenes), 376 cell components (7943 unigenes), and 846 molecular functions (11,750 unigenes). KEGG metabolic pathway analysis matched the DEGs from pre-and post-infection EPC cells to 193 pathways, of which 35 were immune-related, including the Toll-like receptor, cytokine-cytokine receptor interaction, and the JAK-STAT signaling pathways.
机译:本研究旨在鉴定差异表达基因(DEGs)和主要信号转导途径,这些途径与上皮瘤性塞浦路斯鲤(EPC)细胞对同种异体银silver的呼肠孤病毒的免疫应答有关。该研究还为呼肠孤病毒的发病机理和免疫性奠定了理论基础,有助于塞浦路斯鱼类的繁殖。使用新一代的高通量测序技术分析了呼肠孤病毒感染和未感染的EPC细胞。使用生物信息学工具对DEGs进行识别,注释和分类,并确定与呼肠孤病毒感染反应相关的信号途径。数据被组装成92101个重叠群,平均长度为835.24 bp,N50值为1432 nt。所有基因的差异表达分析以错误发现率(FDR)<0.01和倍数变化≥3鉴定了3316个DEG,其中1691个是上调基因,1625个是下调基因,约305个是免疫相关基因。基因本体论(GO)富集分析产生了3941个GO术语的注释,包括2719个生物学过程(37,810个单基因),376个细胞成分(7943个单基因)和846个分子功能(11,750个单基因)。 KEGG代谢途径分析将感染前和感染后EPC细胞的DEG与193种途径进行了匹配,其中35种与免疫相关,包括Toll样受体,细胞因子-细胞因子受体相互作用和JAK-STAT信号通路。

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