首页 | 本学科首页   官方微博 | 高级检索  
     检索      

PCR方法检测鸡减蛋综合征病毒
引用本文:王爱华,李全福,苏杰,孙继国.PCR方法检测鸡减蛋综合征病毒[J].河北农业大学学报,2006,29(4):88-91.
作者姓名:王爱华  李全福  苏杰  孙继国
作者单位:河北北方学院,动物医学系,河北,张家口,075000;河北农业大学,动科院,河北,保定,071001
摘    要:根据已报道的鸡减蛋综合征(Egg drop syndrome 1976 EDS-76)病毒DNA序列,设计合成了1对能扩增300 bp DNA片段的引物,建立了EDS-76病毒的聚合酶链式反应(PCR)诊断方法。该方法对EDS-76病毒标准株AV-127扩增结果为阳性;对鸡传染性支气管炎病毒(IBV)、鸡传染性法氏囊病病毒(IBDV)和鸡新城疫病毒(NDV)的扩增结果均为阴性。结果表明该方法特异且敏感,检测的最低病毒DNA含量达到2.5×10-2pg,PCR检测表明,从试验感染鸡的心脏中不能检测出病毒,肝脏和肾脏只有在感染后7~15 d检出,在试验感染后4~21 d的子宫、血液和4~17 d的脾中均能检测到病毒。

关 键 词:鸡减蛋综合征(EDS-76)病毒  聚合酶链式反应  检测
文章编号:1000-1573(2006)04-0088-04
收稿时间:2005-12-30
修稿时间:2005-12-30

Detection of egg drop syndrome 76 virus by PCR assay
WANG Ai-hua,LI Quan-fu,SU Jie,SUN Ji-guo.Detection of egg drop syndrome 76 virus by PCR assay[J].Journal of Agricultural University of Hebei,2006,29(4):88-91.
Authors:WANG Ai-hua  LI Quan-fu  SU Jie  SUN Ji-guo
Abstract:Polymerize chain reaction(PCR) assay was developed for detection of EDS-76 virus.A pair of primers was synthesized based on the DNA sequence of EDS-76 virus.An expectation of 300bp DNA fragment of EDS-76 virus was amplified by PCR using the primers.The PCR assay is an effective method used to diagnose EDS-76 virus.It could detect as little as 2.5×10~(-2)pg of purified DNA of EDS-76 virus.The crossing-reaction test and sensitive-reaction test indicated that PCR is sensitive and specific.The PCR test showed that the EDS-76 does not exist in the heart,but exists during 7~15 day post infection(DPI) in liver and kidney,4~21 DPI in uterus and blood and 4~17 DPI in spleen.
Keywords:egg drop syndromes virus  PCR  detection
本文献已被 CNKI 万方数据 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号