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作 者:殷相平[1,2] 李志勇[2] 李江涛[2] 李宝玉[2] 兰喜[2] 杨彬[2] 李学瑞[2] 柳纪省[2]
机构地区:[1]甘肃农业大学动物医学院,甘肃兰州730070 [2]中国农业科学院兰州兽医研究所家畜疫病病原生物学国家重点实验室农业部畜禽病毒学重点开放实验室农业部草食动物疫病重点开放实验室,甘肃兰州730046
出 处:《甘肃农业大学学报》2009年第4期19-24,共6页Journal of Gansu Agricultural University
基 金:国家高技术研究发展计划863项目(2006AA10A204);甘肃省科技攻关(2GS0S2-A41-006-02)
摘 要:对狂犬病毒G+N双基因复制缺陷型腺病毒穿梭载体进行转染,以获得融合表过狂犬病毒糖蛋白和核蛋白重组腺病毒,并对其进行生物学特性和免疫学研究.结果表明:将含有狂犬病毒G+N的重组穿梭质粒pAdTrack-CMV/G+N与腺病毒骨架载体pAdEasy-1在大肠杆菌细胞内同源重组,可获得带有目的基因的重组腺病毒载体pAd/G+N,经PacI酶切后转染HEK-293细胞,可获得带有目的基因的重组腺病毒.重组腺病毒在HEK-293细胞中连续传代15代次后,在细胞内的病变时间缩短为20 h以内.经测定,重组腺病毒对HEK-293细胞的TCID50为10-8.0.mL-1,用RT-PCR法可检测到狂犬病毒糖蛋白和核蛋白基因片段;重组腺病毒经口服免疫小白鼠,对狂犬病毒CVS毒株的免疫保护率可达80%.The recombinant adenovirus vector containing the rabies virus (RV) glycoprotein (G) and nucleoprotein (N) was obtained by homologous recorrbination between the recombinant shuttle plasmid pAdTrack-CMV/G+N and pAdEasy vector in E. coli cells, which was designated as pAd/G+N. A recombinant adenovirus containing G and N genes were obtained by transfecting the Pac I digested products of pAd/G+N to HEK-293 cells. The glycoprotein and nucleoprotein genes fragments of rabies virus could be detected in the recombinant adenovirus by RT-PCR. The infection time of the recombinant adenovirus was reduced to less than 20 hours after the virus was the TCID50 of recombinant adenovirus to HEK passaged in HEK-293 cells for 15 generations. Meanwhile, 293 cells reached about 10^-8 · mL^-1. 30 mice were randomly allocated into different groups and orally vaccinated with the recombinant adenovirus. All mice were challenged with rabies virus (CVS strains) in brain at 21 days post vaccination. The protection rate reached 80 % at 10 days post challenge.
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