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作 者:陈玉明[1] 张礼洲[1] 任宪刚[1] 高立[1] 秦立廷[1] 高玉龙[1] 王永强[1] 高宏雷[1] 王笑梅[1] 祁小乐[1]
机构地区:[1]中国农业科学院哈尔滨兽医研究所,兽医生物技术国家重点实验室,禽传染病研究室,黑龙江哈尔滨150001
出 处:《中国畜牧兽医》2014年第1期30-34,共5页China Animal Husbandry & Veterinary Medicine
基 金:国家重点实验室基本科研业务费(SKLVBP201303);现代农业产业技术体系建设专项基金(nycytx-42-G3-01)
摘 要:传染性法氏囊病病毒(infectious bursal disease virus,IBDV)毒株Gx(超强毒株)、F9(中等毒力毒株)、Gt(弱毒株)遗传背景高度相似,但生物学性状差异显著。为研究不同毒力毒株与宿主细胞相互作用的分子细节,本研究将IBDV Gx、F9、Gt毒株的衣壳蛋白VP2基因克隆入pGBKT7载体,分别构建了诱饵载体pGBGxVP2、pGBF9VP2和pGBGtVP2。经Matchmaker Gold Yeast Two-hybrid System验证,结果显示所构建的3个诱饵载体均无自激活作用,对酵母细胞无毒性作用。本研究为利用酵母双杂交系统深入研究IBDV与宿主相互作用奠定了基础。The infectious bursal disease virus (IBDV) strains,Gx (very virulent strain), F9 (intermediate strain) and Gt (attenuated strain) had highly similar genetic background, but their biological characteristics were significantly different. To investigate molecular details of the interaction between various IBDV and their host cells, the genes of VP2 capsid protein of Gx, F9 and Gt were cloned into vector pGBKT7, and the recombinant bait vectors pGBGxVP2, pGBF9VP2 and pGBGtVP2 were constructed. Then the self-activation and toxicity of the bait vectors were tested using the Matchmaker Gold Yeast Two-hybrid System. The results showed that three bait vectors all had no self-activations and toxicities to yeast cells. This research benefited to further investigate the interaction between IBDV and its host cell using the yeast two-hybrid system.
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