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奶牛乳腺炎大肠杆菌PCR的检测
引用本文:任可,刘月焕,王凤龙,步卫东,林健,王金玲,杨龙峰. 奶牛乳腺炎大肠杆菌PCR的检测[J]. 内蒙古农业大学学报(自然科学版), 2006, 27(4): 58-61
作者姓名:任可  刘月焕  王凤龙  步卫东  林健  王金玲  杨龙峰
作者单位:1. 内蒙古农业大学动物科学与医学学院,呼和浩特,010018
2. 北京市农林科学院畜牧所,北京,100097
3. 中国农业大学,北京,100094
摘    要:通过对内蒙古呼和浩特地区分离3株奶牛乳腺炎大肠杆菌16S-23S rRNA间隔区的PCR检测、基因测序和序列比较分析,结果表明:分离菌株12C与参考菌株的同源率为99.9%,DG-25A和DG-23A与参考菌株的同源率为98.9%,3株分离菌株的同源性高。应用PCR检测奶牛乳腺炎大肠杆菌的方法简便、快速、特异,该方法也可广泛用于乳房炎其他病原菌的检测。

关 键 词:奶牛乳房炎  大肠杆菌  16S-23SrRNA间隔区  PCR
文章编号:1009-3575(2006)04-0058-04
收稿时间:2006-09-07
修稿时间:2006-09-07

IDENTIFICATION OF ESCHERICHIA COLI OF COW MASTITIS USING PCR
REN Ke,LIU Yue-huan,WANG Feng-long,BU Wei-dong,LIN Jian,WANG Jin-ling,YANG Long-feng. IDENTIFICATION OF ESCHERICHIA COLI OF COW MASTITIS USING PCR[J]. Journal of Inner Mongolia Agricultural University(Natural Science Edition), 2006, 27(4): 58-61
Authors:REN Ke  LIU Yue-huan  WANG Feng-long  BU Wei-dong  LIN Jian  WANG Jin-ling  YANG Long-feng
Affiliation:1. Inner Mongolia Agricultural University,Huhhot 010018, China; 2. Institute of Animal Husbandry and Veterinary Science, Beijing Academy of Agriculture and Forestry Science,Bering 100097 China; 3. China Agriculture University ,Beijing 100094 , China
Abstract:Three isolates obtained from Huhhot region in Inner Mongolia were investigated by PCR,sequences and analyses with oligonucleotide primers designed according to species-specific parts of the 16S-23S rRNA spacer region of the species.The results showed that the sequence homology was 99.9% between isolate 12C and reference strain and it was 98.9% between strain DG25A,DG23A and reference strain.There was higher homology within three isolates.The PCR amplification of speciesspecific sequences of Escherichia coli in the study offers a rapid,specific and sensitivity method to diagnose the mastitis.
Keywords:Polymerase chain reaction(PCR)  mastitis  Escherichia coli  16S23S rRNA spacer regions
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