鸡传染性法氏囊病病毒dsRNA的提纯与应用  被引量:8

Extraction of Double-stranded RNA of Infectious Bursal Disease Virus

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作  者:孙建和[1] 陆苹[1] 赵渝[1] 李晖[1] 

机构地区:[1]上海交通大学农学院生物技术研究所,上海201101

出  处:《华中农业大学学报》2002年第4期311-314,共4页Journal of Huazhong Agricultural University

基  金:上海市科学技术发展基金资助项目 (0 1JC14 0 3 4)

摘  要:用传染性法氏囊病病毒 (IBDV)攻击 4周龄的非免疫鸡 ,以超速离心法从感染鸡法氏囊组织中分离、纯化IBDV ,应用蛋白酶K消化和Trizol(异硫氰酸胍 -酚 -氯仿法 )处理 2种方法从纯化的IBDV中抽提dsRNA。通过低熔点琼脂糖割胶 -酚 -氯仿抽提可获得纯化的dsRNA ,研究发现应用蛋白酶K消化获得的纯化RNA产量高 ,用其作模板进行RT -PCR可扩增IBDV基因组全长cDNAA片段和B片段、VP2基因和VP2 - 4 - 3基因。week old chickens unaffected by infectious bursal disease virus (IBDV) were challenged with Shanghai strains of IBDV orally. The virion were purified through ultracentrifuge from affected bursa. A proteinase K digestion based approach and Trizol RNA extraction method were used to extract dsRNA of IBDV from purified virions. The yield of dsRNA extracted by proteinase K digestion based approach was higher than that of Trizol method. dsRNA extracted by proteinase K digestion was more suitable for the amplification of full length cDNA of IBDV by long and accurate PCR.

关 键 词:鸡传染性法氏囊病病毒 DSRNA 提纯 应用 

分 类 号:S852.659.4[农业科学—基础兽医学] S858.312.6[农业科学—兽医学]

 

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