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传染性法氏囊病病毒的PCR引物设计与Internet检索分析
引用本文:荣俊,余龙江.传染性法氏囊病病毒的PCR引物设计与Internet检索分析[J].湖北农学院学报,2000,20(1):49-52.
作者姓名:荣俊  余龙江
作者单位:华中理工大学生命科学院湖北武汉 430074
基金项目:湖北省教育厅科研项目,,
摘    要:研究了传染性法氏囊病病毒(IBDV)A片断的cDNA的结构,并使用PrimerDesign引物设计软件,在VP5和VP2的重叠基因区设计了一对引物,各种IBDV毒株在此部位有非常高的同源性,在对引物进行Internet检索中得到了证实。经过对4种IBDV的疫苗标准毒株,1种野毒株,1例病鸡标本试检测,验证引物设计符合要求,具有良好的适应性和较高的灵敏度。

关 键 词:  IBDV  PCR  引物设计  Internet检索  早期诊断
文章编号:1004-3888(2000)01-0049-04
修稿时间:1999年9月18日

Design of Infectious Bursal Disease Virus PCR Primer and Interne t Retrieval
RONG Jun,YU Long jiang.Design of Infectious Bursal Disease Virus PCR Primer and Interne t Retrieval[J].Journal of Hubei Agricultural College,2000,20(1):49-52.
Authors:RONG Jun  YU Long jiang
Abstract:Based on the study of segment A of the infectious bursal disease virus(IBDV) cDNA, a pair of primers was designed with the PrimerDesign software. This pair of primers is in the overlapping area of VP 5 and VP 2 where the sequence is highly homologous, which was verified when searching them in the Internet. Four standard virus strains, one wild strain and one IBDV strain from the cloacal bursa of diseased chicken had been amplified successfully with the primers. Two other viruses, which could result in other disease of chicken and one healthy chicken's cloacal bursa had given negative results. This proved that the primers accord with the demand of the amplification of IBDV,and have good adjustability and high sensitivity.
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