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

应用聚合酶链反应检测鉴别火鸡支原体方法的建立
引用本文:谢芝勋,邓显文,谢志勤.应用聚合酶链反应检测鉴别火鸡支原体方法的建立[J].中国预防兽医学报,2000,22(3):215-217.
作者姓名:谢芝勋  邓显文  谢志勤
作者单位:广西兽医研究所,南宁
基金项目:广西留学回国人员基金,国家非教育系统留学回国人员择优项目资助
摘    要:根据基因库中火鸡支原体(MM)16S rRNA基因序列(Genebank U04649),设计了一对跨幅为850bp的引物,用这对引物对4禽侏火鸡支原体标准菌株和6种其它禽病病原体进行PCR扩增,结果4禽株鸡支原体菌株均得到片段大小与预期设计相一致的850bp的PCR扩增产物,而其它6种禽病病原体(包括MG、MS和MI)的扩增结果则均为阴性,该PCR能检出100fg的火鸡支原体的DNA模板。

关 键 词:火鸡支原体  聚合酶链反应  检测  鉴别  16S  rRNA
修稿时间:1999-11-25

Detection and Identification of Mycoplasma Meleagridis by Polymerase Chain Reaction
XIE Zhixun,DENG Xianweng,XIE Zhiqin,PANG Yaoshang,LIU Jiabo.Detection and Identification of Mycoplasma Meleagridis by Polymerase Chain Reaction[J].Chinese Journal of Preventive Veterinary Medicine,2000,22(3):215-217.
Authors:XIE Zhixun  DENG Xianweng  XIE Zhiqin  PANG Yaoshang  LIU Jiabo
Abstract:A set of primers,XZ19、XZ20 were designed accord ing to the&127;sequence of 16s rRNA gene of Mycoplasma Meleagridis (MM) from Genebank U04649. A MM specific 850-base pair DNA product was amplified by thes e&127;primers from four MM reference strains,but not from six other avian pathogenic virus and bacteria (including MG、MS and MM). As little as 100fg of&127;MM DNA was detected using gel electrophroesis.
Keywords:Mycoplasma Meleagridis  Polymerase Chain Reaction  Detection
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