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传染性法氏囊病RT-PCR诊断方法研究
引用本文:荣俊,刘晓娜,程太平,杨待建.传染性法氏囊病RT-PCR诊断方法研究[J].中国预防兽医学报,2000(Z1).
作者姓名:荣俊  刘晓娜  程太平  杨待建
作者单位:湖北农学院动物科学系!荆州 434103
摘    要:本文在研究传染性法氏囊病病毒的A片断cDNA结构的基础上,用Primer  Design引物设计软件,在VP_5和VP_2的重叠基因区设计了一对引物,使用该引物对6种IBDV的标准毒株,10例自然发病病鸡组织标本,8例IBDV J_1C_7F_3种毒株攻毒病理法氏囊组织标本,进行了RT-PCR检测均得到了阳性的扩增结果。2种参考鸡病病毒和8例健康鸡的法氏囊组织在同样条件下进行扩增均为阴性结果。本法具有扩增方法简单,对各种病毒株的适应性广,特异性高,检测成本较低的特点。

关 键 词:IBDV  RT-PCR  诊断试剂

Diagnosis of IBDV with RT-PCR
RONG Jun,LIU Xiaona,CHENG Taiping,YANG Daijian.Diagnosis of IBDV with RT-PCR[J].Chinese Journal of Preventive Veterinary Medicine,2000(Z1).
Authors:RONG Jun  LIU Xiaona  CHENG Taiping  YANG Daijian
Abstract:After a carefully study on segment A of the cDNA of infectious bursal disease virus(IBDV), a pair of primers were designed with the Primer Design software.This primer pair is in the overlapping area of VP5 and VP2 where the sequence is highly homologous.6 stan- dard virus strains, 10 tissue specimen of natural diseased chickens and 8 pathology cloacial bursa specimen of IBDV J1C7F3 attacking test chickens had been amplified successfully with this pair of primers. 2 other comparison virus strains and 8 healthy chickens' cloacial bursa had given negative results. The system has the following features: it has wide spread adjustability to various kinds of virus; the specificity is high; the process is ease to oerate; and the test cost is low.
Keywords:IBDV  RT-PCR  Diagnosis reagent
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