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作 者:吕英姿[1] 曹永长[1] 陈峰[1] 毕英佐[1]
机构地区:[1]华南农业大学动物科学学院,广东广州510642
出 处:《华南农业大学学报》2002年第2期70-73,共4页Journal of South China Agricultural University
基 金:国家自然科学基金资助项目 (39870 5 5 0 ) ;广东省自然科学基金资助项目 (96 0 4 4 9)
摘 要:在体外分别构建了 3种重组表达质粒 :含传染性囊病病毒GZ911株VP2基因的pGVP2、含HK4 6株VP2基因的pHVP2以及含HK4 6株 5’ -端序列 (包括非编码区、VP5和VP2基因 )的pHVP2 +5 .用不同的重组质粒转染原代鸡胚成纤维细胞 (CEF) ,在转染后 0、14、38h ,收集对照组和转染组细胞 ,用酶联免疫吸附试验检测CEF中降解DNA量 .结果 ,在 14和 38h ,各组细胞中测得的Dλ 值均为转染pHVP2 +5组最大 ,其次为转染pHVP2、pGVP2的组 ,并都大于其他对照组 ,表明 2个IBDV毒株的VP2蛋白在CEF中表达后都能诱导CEF发生凋亡 ,但不同毒株的VP2蛋白诱导CEF凋亡的能力不同 ;Three recombinant plasmids,pGVP2 and pHVP2 containing VP2 gene of IBDV strain GZ911 and HK 46 respectively, and pHVP2+5 containing 5' terminal sequence including 5' non coding region,VP5 gene and VP2 gene, were cloned. These three plasmids were used to transfect chicken embryo fibroblasts(CEF). At 0,14,38 h post transfection, cells in different groups were collected and the amount of DNA fragments was measured with enzyme linked immunosorbent assay(ELISA). At 14 and 38 h posttransfection, cells transfected with pHVP2+5 produced the highest D λ , cells transfected with pHVP2 produced intermediate D λ , and pGVP2 produced the lowest D λ . All of which were higher than control groups. These results showed that VP2 of two IBDV strains was able to induce apoptosis when expressed in CEF, but the VP2 of different strains varied in the capacity to induce apoptosis. The apoptosis in CEF induced by VP2 was enhanced by VP5.
关 键 词:传染性囊病病毒 VP2蛋白 VP5蛋白 细胞凋亡 鸡胚成纤维细胞 致病机理
分 类 号:S858.315.3[农业科学—临床兽医学]
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