布鲁菌S2疫苗株的核酸探针检测方法的建立  

Establishment of Nucleic Acid Probes for Detecting Brucella Vaccine Strain S2

作　　者：张岩[1] 李建[1] 宫利娜 高航飞[1] 李旭东[1] 安维雪 申之义[1] 

机构地区：[1]内蒙古农业大学兽医学院农业部动物疾病临床诊疗技术重点实验室,内蒙古呼和浩特010018

出　　处：《动物医学进展》2015年第8期51-54,共4页Progress In Veterinary Medicine

摘　　要：为了鉴别布鲁菌疫苗免疫和自然感染,建立鉴别布鲁菌S2疫苗株与其他菌株的斑点杂交法。针对布鲁菌基因序列保守区S2疫苗株与其他菌株的差异设计探针,同时根据差异部分设计引物进行PCR扩增;PCR产物经过回收、纯化、变性后固定在NC膜上,与探针杂交、显色。结果显示,PCR引物能够对S2疫苗株扩增出约330bp的核酸片段,对其他布鲁菌扩增出约360bp的核酸片段;探针只能和S2疫苗株的PCR产物杂交,最低检测到10pg DNA,能够在10h内鉴别出布鲁菌S2疫苗株。To Explore the dot blot hybridization for discrimination of Brucella live vaccine strain S2 from field strains,according to the difference of geneme between B.suis vaccine strain S2 and other strains in NCBI,specific primers and probes were designed and labeled by DIG high prime.PCR products were recov-ered,purified,denatured and fixed to the NC membrane,then hybridized with the probe labeled by DIG high prime and detected.330 bp fragment could be amplified from strains of vaccine strain S2,and 360 bp from other Brucella strains.The probe was specific and no cross hybridization with other Brucella strains. 10 pg DNA of Brucella live vaccine strain S2 could be discriminated in 10 h by the dot blot hybridization.

关 键 词：布鲁菌 检测技术 斑点杂交 

分 类 号：S855.12[农业科学—临床兽医学]