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

水貂肠炎细小病毒PCR检测方法的建立和应用
引用本文:张海玲,闫喜军,柴秀丽,吴威,易立,罗国良,田洪宇,邵西群,王凤雪.水貂肠炎细小病毒PCR检测方法的建立和应用[J].特产研究,2007,29(2):1-3.
作者姓名:张海玲  闫喜军  柴秀丽  吴威  易立  罗国良  田洪宇  邵西群  王凤雪
作者单位:中国农业科学院特产研究所,吉林,吉林,132109
基金项目:科技部科研院所社会公益研究专项基金
摘    要:根据GenBank上已发表的水貂肠炎细小病毒基因序列,在其编码VP2结构蛋白基因的高度保守区内,设计合成1对特异性引物,建立水貂肠炎细小病毒PCR诊断方法。经过敏感性及特异性检测,该引物能与MEV标准株和地方分离株核酸发生特异性结合,扩增出一段长度为570bp的DNA片段,而与CDV、ADV等病毒的PCR反应均呈阴性。设计的该对引物可用于MEV的临床检测。

关 键 词:水貂病毒性肠炎  引物
文章编号:1001-4721(2007)02-0001-03
修稿时间:2007-04-29

Establishment and Application of PCR for Detection of Mink Enteritis Virus
ZHANG Hai-ling,YAN Xi-jun,CHAI Xiu-li,WU Wei,YI Li,LUO Guo-liang,TIAN Hong-yu,SHAO Xi-qun,WANG Feng-xue.Establishment and Application of PCR for Detection of Mink Enteritis Virus[J].Special Wild Economic Animal and Plant Research,2007,29(2):1-3.
Authors:ZHANG Hai-ling  YAN Xi-jun  CHAI Xiu-li  WU Wei  YI Li  LUO Guo-liang  TIAN Hong-yu  SHAO Xi-qun  WANG Feng-xue
Institution:Institue of Special Wild Economic Animal and Plant Science, CAAS. Jilin 132109, China
Abstract:Two primers were designed and synthesized according to the nucleocapasid gene sequence of mink enteritis virus from GenBank,and used to detect mink enteritis virus.Special products of 570bp size were amplified by these primers from MEV vaccine and suspected cases but not from CDV,CAV and ADV strains.The results indicated that the PCR assay of MEV was proved to be specific and sensitive.It is feasible method for rapid diagnosis of MEV.
Keywords:PCR
本文献已被 CNKI 维普 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