Shi Zixue, Sun Jinfu, Guo Huancheng, Tu Changchun
College of Animal Science and Veterinary Medicine, Jilin University, 5333 XiAn Da Road, Changchun 130062, PR China.
Institute of Veterinary Sciences, Academy of Military Medical Sciences, 1068 Qinglong Road, Changchun 130062, PR China.
J Gen Virol. 2009 Jul;90(Pt 7):1670-1680. doi: 10.1099/vir.0.009415-0. Epub 2009 Mar 4.
Classical swine fever (CSF), caused by a virus of the same name (CSFV), is a highly contagious swine pyrexic disease featuring extensive haemorrhagic lesions and leukopenia, but little is known about the molecular mechanisms of its pathogenesis. To gain insight into the interaction between the virus and host cells, microarray analyses were performed to detect alterations in genomic expression of pig peripheral blood leukocytes (PBLs) following CSFV infection. Three healthy pigs were inoculated with a lethal dose of highly virulent CSFV strain Shimen. PBLs were isolated at the onset of typical clinical signs and total RNA was subjected to microarray analyses with Affymetrix Porcine Genome Array GeneChips. Of all 20,201 pig genes arrayed in the chip, 1745 showed altered expression (up- or downregulation) after infection. These were classified into eight functional groups, relating to cell proliferation (3.6%), immune response (2.1%), apoptosis (1.4%), kinase activity (1.4%), signal transduction (1.4%), transcription (0.7%), receptor activity (0.7%) and cytokines/chemokines (0.4%). The remaining 88.3% of genes had unknown functions. Alterations in genomic expression were confirmed by real-time RT-PCR of selected cellular genes and Western blotting of annexin 2, a cellular protein relating to virus infection. The observed expression changes of numerous genes involved in immune and inflammatory responses and in the apoptosis process indicate that CSFV has developed sophisticated mechanisms to cause leukopenia in infected pigs. These data provide a basis for exploring the molecular pathogenesis of CSFV infection through an understanding of the interaction between viral and cellular components.
经典猪瘟(CSF)由同名病毒(CSFV)引起,是一种高度传染性的猪发热性疾病,其特征为广泛的出血性病变和白细胞减少,但对其发病机制的分子机制知之甚少。为了深入了解病毒与宿主细胞之间的相互作用,进行了微阵列分析,以检测CSFV感染后猪外周血白细胞(PBL)基因组表达的变化。三只健康猪接种了致死剂量的高致病性CSFV石门株。在典型临床症状出现时分离PBL,并使用Affymetrix猪基因组阵列基因芯片对总RNA进行微阵列分析。芯片上排列的所有20201个猪基因中,1745个在感染后显示表达改变(上调或下调)。这些基因被分为八个功能组,与细胞增殖(3.6%)、免疫反应(2.1%)、细胞凋亡(1.4%)、激酶活性(1.4%)、信号转导(1.4%)、转录(0.7%)、受体活性(0.7%)以及细胞因子/趋化因子(0.4%)有关。其余88.3%的基因功能未知。通过对选定细胞基因的实时RT-PCR和与病毒感染相关的细胞蛋白膜联蛋白2的蛋白质印迹法,证实了基因组表达的变化。观察到的许多参与免疫和炎症反应以及细胞凋亡过程的基因表达变化表明,CSFV已经形成了复杂的机制,导致感染猪出现白细胞减少。这些数据为通过了解病毒和细胞成分之间的相互作用来探索CSFV感染的分子发病机制提供了基础。