当前位置: 首页 > 文章 > 利用BrdU在CEF(TK~+)细胞中筛选TK~-重组鸡痘病毒 中国兽医学报 2001,21 (6) 543-545
Position: Home > Articles > Selection of TK~- Recombinant Fowlpox Virus in CEF Cell (TK~+) in the Presence of BrdU Chinese Journal of Veterinary Science 2001,21 (6) 543-545

利用BrdU在CEF(TK~+)细胞中筛选TK~-重组鸡痘病毒

作  者:
郭志儒;金宁一;方厚华;罗坤;夏志平;殷震
单  位:
解放军军需大学军事兽医研究所
关键词:
BrdU;鸡痘病毒;TK基因;重组病毒
摘  要:
将新城疫病毒 (NDV)四平株 HN基因 ,插入不含报告基因、以 TK为侧翼的鸡痘病毒表达载体 p UTA- 2中的复合启动子下游 ,获得重组表达质粒 p UTA- 2 HN。将重组表达质粒转染鸡痘病毒 (FPV)感染的鸡胚成纤维细胞 (CEF) ,培养、收获病毒后 ,用含 40 m g/ L 5 -溴 - 2 -脱氧尿嘧啶 (Brd U )的培养液 ,在 CEF(TK+)细胞中筛选培养 2代 ,然后用不含 Brd U的培养液进行病毒蚀斑纯化 ,成功筛选出表达 NDV HN蛋白的 TK-重组鸡痘病毒
译  名:
Selection of TK~- Recombinant Fowlpox Virus in CEF Cell (TK~+) in the Presence of BrdU
作  者:
GUO Zhi-ru, JIN Ning-yi, FANG Hou-hua, LUO Kun, XIA Zhi-ping, YIN Zhen (The Military Veterinary Institute, Quartermaster University of PLA, Changchun 130062, China)
关键词:
BrdU; fowlpox virus; TK gene; recombinant virus
摘  要:
A recombinant expression plasmid pUTA-2HN was constructed by inserting the HN gene of Newcastle disease virus(NDV) strain Siping, into the SmaⅠ site downstream of a hybrid poxvirus promoter which is flanked by the TK gene of fowlpox virus(FPV) strain 282E4. For production and selection recombinant fowlpox virus expressing the HN gene of NDV and without containing additional reporter gene, the constructed pUTA-2HN was firstly transfected into chicken embryo fibroblast(CEF) cells preinfected with FPV strain 282E4, then the viruses resulted from the transfection were selected for 2 passages by culturing in CEF cells with MEM medium containing 40 mg/L 5-bromo-2′deoxy-uridine(BrdU). The selected viruses were plaque-purified in CEF cells cultured with MEM media without BrdU. After Western blot analysis the lysate of CEF cells which were infected by the purified FPV, recombinant FPVs (rFPVs) expressing the HN protein were obtained. This indicated that rFPVs containing a foreign gene interrupted TK gene (TK -) could be selected in the CEF(TK +) cell in the presence of BrdU.

相似文章

计量
文章访问数: 10
HTML全文浏览量: 0
PDF下载量: 0

所属期刊

推荐期刊