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

新疆阿拉尔垦区猪嗜血支原体PCR检测方法的建立
引用本文:赵爱云,何强,井波.新疆阿拉尔垦区猪嗜血支原体PCR检测方法的建立[J].安徽农业科学,2011,39(14):8619-8621.
作者姓名:赵爱云  何强  井波
作者单位:新疆生产建设兵团塔里木畜牧科技重点实验室塔里木大学动物科学学院;
基金项目:新疆生产建设兵团塔里木畜牧科技重点实验室开放课题项目(HS20902)
摘    要:目的]掌握阿拉尔垦区猪嗜血支原体的流行现状。方法]根据GenBank上发表的猪嗜血支原体16S rRNA基因组序列(U88565)设计1对特异性引物,对采自新疆阿拉尔垦区的样品进行PCR扩增,并将其产物克隆到pBR322载体后测序。结果]扩增出的片段为0.836 kb。同源性分析结果表明,该序列与猪嗜血支原体参考基因组序列同源性为99.47%,反映出我国分离株与国外株基因同源性较高。结论]建立了一种猪嗜血支原体PCR检测方法,该方法为猪嗜血支原体病的快速诊断及流行病学调查提供了新的手段,并为相关基因的表达及功能研究奠定了基础。

关 键 词:猪嗜血支原体  PCR  克隆

PCR Detection Method of Swine Mycoplasma haemophilus in Alar Area
ZHAO Ai-yun et al.PCR Detection Method of Swine Mycoplasma haemophilus in Alar Area[J].Journal of Anhui Agricultural Sciences,2011,39(14):8619-8621.
Authors:ZHAO Ai-yun
Institution:ZHAO Ai-yun et al(Key Laboratory of Animal Science and Technology of Tarim Basin,Xinjiang Production and Construction Corps,College of Animal Sciences,Tarim University,Alar,Xinjiang 843300)
Abstract:Objective] The current situation of the prevalence of swine mycoplasma haemophilus in the Alar area was mastered.Method] For the PCR amplification of the samples selected from the Alar area of Xinjiang 1 pair of specific primers was designed according to the genome sequence of 16S rRNA(U88565) of swine mycoplasma haemophilus published in GenBank and the products were sequenced after they were cloned into the pBR322 vector.Result] The amplified fragment was 0.836 kb.The analysis showed that the homology o...
Keywords:Swine mycoplasma haemophilus  PCR  Cloning  
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