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首页> 外文期刊>Virus Research: An International Journal of Molecular and Cellular Virology >Global transcriptional profiles in peripheral blood mononuclear cell during classical swine fever virus infection.
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Global transcriptional profiles in peripheral blood mononuclear cell during classical swine fever virus infection.

机译:猪瘟病毒感染过程中外周血单核细胞的整体转录谱。

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摘要

Classical swine fever virus (CSFV) is an etiologic agent that causes a highly contagious disease in pigs. Laying a foundation to solve problems in its pathogenic mechanism, microarray analysis was performed to detect the gene transcriptional profiles in peripheral blood mononuclear cells (PBMC) following infection with a Chinese highly virulent CSFV strain Shimen. Three susceptible pigs were inoculated intramuscularly with a lethal dose (1.0x10(6) TCID(50)) of CSFV. Pigs showed classical CSF signs, depletion of lymphocytes and monocytes consistent with CSFV infection, and the CSFV genome was also confirmed in the PBMC. The PBMC were isolated at 1, 3, 6 and 9 days post-inoculation (dpi). Total RNA were extracted and subjected to microarray analysis. Data showed that expression of 847 genes wherein 467 genes were known function and the remaining 380 genes were unknown function, and 541 up- and 306 down-regulation, altered after infection. There were 54, 181, 438 and 354 up- and 61, 120, 218 and 145 down-regulated genes presented on 1, 3, 6 and 9dpi, respectively. These genes were involved in immune response (14.5%), apoptosis (3.3%), signal transduction (7.6%), transcription (4.4%), metabolism (11%), transport (3.9%), development (6.8%) and cell cycle (3.7%). Results demonstrated its usefulness in exploring the pathogenic mechanisms of CSFV.
机译:古典猪瘟病毒(CSFV)是引起猪高度传染性疾病的病原体。为解决其致病机制中的问题奠定基础,进行了微阵列分析,以检测中国高毒力CSFV株石门病毒感染后外周血单核细胞(PBMC)的基因转录谱。用致死剂量(1.0x10(6)TCID(50))的CSFV肌肉注射三只易感猪。猪表现出经典的CSF体征,与CSFV感染一致的淋巴细胞和单核细胞耗竭,并且在PBMC中也证实了CSFV基因组。在接种后1、3、6和9天(dpi)分离PBMC。提取总RNA并进行微阵列分析。数据显示,感染后847个基因的表达发生了变化,其中467个基因为已知功能,其余380个基因为未知功能,并且541个上调和306个下调。分别以1、3、6和9dpi呈现54、181、438和354个上调基因以及61、120、218和145个下调基因。这些基因参与免疫应答(14.5%),细胞凋亡(3.3%),信号转导(7.6%),转录(4.4%),新陈代谢(11%),运输(3.9%),发育(6.8%)和细胞周期(3.7%)。结果证明了其在探索CSFV的致病机制中的有用性。

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