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首页> 外文期刊>Archives of virology >The gene expression profile of porcine alveolar macrophages infected with a highly pathogenic porcine reproductive and respiratory syndrome virus indicates overstimulation of the innate immune system by the virus
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The gene expression profile of porcine alveolar macrophages infected with a highly pathogenic porcine reproductive and respiratory syndrome virus indicates overstimulation of the innate immune system by the virus

机译:感染高致病性猪繁殖与呼吸综合征病毒的猪肺泡巨噬细胞的基因表达谱表明该病毒过度刺激了先天免疫系统

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Since the highly pathogenic porcine reproductive and respiratory syndrome virus (HP-PRRSV) variant emerged in 2006, it has caused death in more than 20 million pigs in China and other Southeast Asian countries, making it the most destructive swine pathogen currently in existence. To characterize the cellular responses to HP-PRRSV infection, the gene expression profile of porcine alveolar macrophage (PAM) cells, the primary target cells of PRRSV, was analyzed in HP-PRRSV-infected and uninfected PAMs by suppression subtractive hybridization. After confirmation by Southern blot, genes that were differentially expressed in the HP-PRRSV-infected and uninfected PAMs were sequenced and annotated. Genes that were upregulated mainly in HP-PRRSV-infected PAM cells were related to immunity and cell signaling. Among the differentially expressed genes, Mx1 and HSP70 protein expression was confirmed by western blotting, and IL-8 expression was confirmed by ELISA. In PAM cells isolated from HP-PRRSV-infected piglets, the differential expression of 21 genes, including IL-16, TGF-beta type 1 receptor, epidermal growth factor, MHC-I SLA, Toll-like receptor, hepatoma-derived growth factor, FTH1, and MHC-II SLA-DRB1, was confirmed by real-time PCR. To our knowledge, this is the first study to demonstrate differential gene expression between HP-PRRSV-infected and uninfected PAMs in vivo. The results indicate that HP-PRRSV infection excessively stimulates genes involved in the innate immune response, including proinflammatory cytokines and chemokines.
机译:自从2006年出现高致病性猪繁殖与呼吸综合征病毒(HP-PRRSV)变种以来,它已在中国和其他东南亚国家/地区造成超过2000万头猪死亡,使其成为目前存在的最具破坏性的猪病原体。为了表征细胞对HP-PRRSV感染的反应,通过抑制消减杂交分析了猪肺泡巨噬细胞(PAM)细胞(PRRSV的主要靶细胞)的基因表达谱,分析了HP-PRRSV感染和未感染的PAM。在通过Southern印迹确认后,对在HP-PRRSV感染和未感染的PAM中差异表达的基因进行测序和注释。主要在HP-PRRSV感染的PAM细胞中上调的基因与免疫力和细胞信号转导有关。在差异表达的基因中,通过western印迹证实了Mx1和HSP70蛋白的表达,并且通过ELISA证实了IL-8的表达。在从HP-PRRSV感染的仔猪中分离出的PAM细胞中,IL-16,TGF-β1型受体,表皮生长因子,MHC-I SLA,Toll样受体,肝癌衍生的生长因子等21种基因的差异表达实时PCR证实了FTH1和MHC-II SLA-DRB1。据我们所知,这是首次证明体内感染HP-PRRSV的PAM与未感染的PAM之间存在差异基因表达的研究。结果表明,HP-PRRSV感染过度刺激了与先天免疫反应有关的基因,包括促炎细胞因子和趋化因子。

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