摘要:本课题研究了传染性法氏囊病(IBD)重组火鸡疱疹病毒的构建策略。以HVT FC126基因组的非必需区UL44-UL45为插入位点,构建带有大肠杆菌黄嘌吟-鸟嘌吟磷酸转移酶基因序列(gpt)标记的有HVT转移载体质粒pUAB-gpt。然后由人工合成Pec启动子,构建表达传染性法氏囊病毒(IBDV)VP2嵌合法氏囊素三肽(BS10)表达盒并克隆入pUAB-gpt,获得转移载体质粒pUAB-Pec-BS10-VP2-gpt。将该HVT转移载体与HVT DNA共转染鸡胚成纤文细胞(CEF),待出现病毒噬斑后,利用霉酚酸(MPA)阻断核酸代谢途径 ,经过筛选获得重组病毒rHVT-Pec-BS10-VP2。Western blotting分析,在53 kDa处出现一条特异蛋白条带。IBDV抗体夹心ELISA检测,重组病毒呈阳性反应,抗原效价达1.6×103。结果表明,IBD重组火鸡疱疹病毒构建成功。28051 毕业论文关键词:鸡传染性法氏囊病;VP2基因;法氏囊素三肽;重组火鸡疱疹病毒
Construction of recombinant Turkey Herpesvirus expressing infectious bursal disease virus VP2 and bursal cysteoid chimeric gene
Abstract: The construction of recombinant turkey herpesviruses of infectious bursal disease virus VP2 and bovine cysteine tripeptide chimeric gene was studied. Non essential region UL44-UL45 of HVT FC126 genome was selected as insertion sites. Using the selection marker Eco-gpt Xanthine-guanine phosphoribosyl transferase (gpt), plasmid pUAB-gpt were constructed. Then, BS10-VP2 expression cassette was constructed containing synthesised Pec promoters and then was cloned into the plasmid pUAB-gpt to obtain the transfer vector of turkey herpesvirus pUAB-Pec-BS10-vp2-gpt. Finall, transfer vector and total DNA of HVT infected cells were cotransfected into chicken embryo fibroblasts (CEFs). After six rounds of selection in medium containing mycophenolic acid, xanthine and hypoxanthine, recombinant virus rHVT-Pec-BS10-VP2 was obtained. Western blotting revealed that the calculated protein of approximately 53 kDa was expressed in the CEF cells. and recombinant virus was positive with antigen titer of 1.6×103 by IBDV sandwich ELISA. Recombinant IBD turkey herpesvirus is proved successful.
Key words: IBDV; VP2gene ;BS10; recombinant rHVT
目 录