首页> 外文期刊>Infection, Genetics and Evolution: Journal of Molecular Epidemiology and Evolutionary Genetics in Infectious Diseases >RNA sequencing analyses of gene expressions in a canine macrophages cell line DH82 infected with canine distemper virus
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RNA sequencing analyses of gene expressions in a canine macrophages cell line DH82 infected with canine distemper virus

机译:犬巨噬细胞中基因表达的RNA测序分析DH82感染犬瘟热病毒

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Virulent morbillivirus infections, including Meals Virus (MeV) and Canine Distemper Virus (CDV), caused severe immune suppression and leukopenia, while attenuated vaccine strains developed protective host immune responses. However, the detailed molecular foundations of host antiviral responses were poorly characterized. In order to better understand the interactions between attenuated vaccine and host antiviral responses, the global gene expression changes in CDV-11-infected DH82 cells, a macrophage-derived cell line from canine, were investigated by transcriptomic analysis, and portions of results were confirmed with quantitative RT-PCR. The results exhibited that 372 genes significantly up-regulated (p < .01) and 119 genes were significantly down-regulated (p < .01) in CDV-infected macrophages DH82 at 48 h p.i.. The enriched functions of the significantly up-regulated (p < .01) genes were closely associated with interferon stimulated genes (ISGs), chemokine genes and pro-inflammatory factor genes. Gene ontology and pathway analysis of differentially expressed genes (DEGs) revealed that the most significantly involved pathways in CDV-infected DH82 cells were NF-kappa B and TNF signaling pathway, cytokine-cytokine receptor interaction, and pathogen associated molecular patterns (PAMPs), such as Toll-like, RIG-I-like and NOD-like receptor signalings. Thus, the findings indicated that pattern recognition receptors (PRRs) possibly mediated host innate and protective antiviral immune responses in CDV-11 infected DH82 cells.
机译:毒性Morbillivirus感染,包括膳食病毒(MEV)和犬瘟热病毒(CDV),导致严重的免疫抑制和白细胞减少,而减毒疫苗菌株产生保护宿主免疫应答。然而,宿主抗病毒反应的详细分子基础特征差。为了更好地了解减毒疫苗和宿主抗病毒反应之间的相互作用,通过转录组分析研究了CDV-11感染的DH82细胞中的全球基因表达在CDV-11感染的DH82细胞中变化,并确认了部分结果的结果用定量RT-PCR。结果表明,在48小时PI的CDV感染的巨噬细胞DH82中显着下调372个基因(p <.01)和119个基因。富集的富集功能明显上调(P <.01)基因与干扰素刺激基因(ISG),趋化因子基因和促炎因子基因密切相关。差异表达基因(DEGS)的基因本体和途径分析表明,CDV感染的DH82细胞中最显着的途径是NF-κB和TNF信号通路,细胞因子 - 细胞因子受体相互作用和病原体相关分子模式(PAMPs),如Toll样,钻机 - I样和点状的受体信号。因此,结果表明,模式识别受体(PRRS)可能介导的Host先天内先生先天内酯和保护性抗病毒免疫应答。

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