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

鸡毒支原体PCR检测方法的建立
引用本文:秦璐璐.鸡毒支原体PCR检测方法的建立[J].动物医学进展,2009,30(2).
作者姓名:秦璐璐
作者单位:安徽农业大学动物科技学院,安徽合肥,230036
摘    要:根据已发表的鸡毒支原体种特异性序列fMG-2设计1对引物,建立检测鸡毒支原体的PCR方法.该法对鸡毒支原体能特异性扩增726 bp的目的片段,而对其他禽病原DNA模板的扩增结果为阴性.建立的PCR方法对鸡毒支原体的最少检出量为3 Pg.用建立的PCR方法对临床采集的样品进行检测,同时对相应的样品进行细菌分离,结果临床样品PCR的阳性检出率为20.5%,细菌分离培养的阳性率为0.9%,表明PCR的敏感性高于细菌分离鉴定.

关 键 词:鸡毒支原体  聚合酶链反应  检测  分离鉴定

Establishment of PCR for Detection of Mycoplasma gallisepticum
QIN Lu-lu.Establishment of PCR for Detection of Mycoplasma gallisepticum[J].Progress In Veterinary Medicine,2009,30(2).
Authors:QIN Lu-lu
Institution:College of Animal Sicence and Technologe;Anhui Agriculture University;Hefei;Anhui;230036;China
Abstract:A pair of primers was designed based on fMG-2 sequences of avian Mycoplasma.The primers selectively amplified a 726 bp product from Mycoplasma gallisepticum(MG),but did not amplify the DNA or RNA of other bacteria or viruses.The detection threshold of PCR for MG was 3 pg.The samples detected by PCR,and isolation and identification.Using PCR,20.5% of field samples was positively detected,it was higher than that of isolation and identification.The results indicated that this technique is a useful screening as...
Keywords:Mycoplasma gallisepticum  PCR  detection  isolation and identification  
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