检索规则说明:AND代表“并且”;OR代表“或者”;NOT代表“不包含”;(注意必须大写,运算符两边需空一格)
检 索 范 例 :范例一: (K=图书馆学 OR K=情报学) AND A=范并思 范例二:J=计算机应用与软件 AND (U=C++ OR U=Basic) NOT M=Visual
作 者:谭秋杉[1,2] 高利荣[1] 王晓杜[1] 蒋昭君[1] 沈蔷[1] 张先福[1,2]
机构地区:[1]浙江农林大学亚热带森林培育国家重点实验室培育基地,浙江临安311300 [2]浙江农林大学动物科技学院,浙江临安311300
出 处:《中国预防兽医学报》2014年第1期50-53,共4页Chinese Journal of Preventive Veterinary Medicine
基 金:国家自然科学基金(31372501);浙江省自然科学基金(LY13C180001)
摘 要:为建立一种快速诊断鸭疫里默氏杆菌(RA)病的方法,本研究根据NCBI登录的ATCC 11845菌株(CP003388.1)的16S rRNA基因保守序列设计引物,对标准株和疑似感染RA的病料样品进行检测,建立RA PCR检测方法。结果显示,6株RA标准株(包括1、2、10和11血清型)和2个疑似RA感染的病料样品,均能够扩增出698 bp的特异性片段,而鸭大肠杆菌和鸭沙门氏菌扩增均呈阴性。测序分析表明,疑似病料样品中扩增的片段与ATCC 11845菌株相应片段同源性达99.9%。PCR敏感性试验检测显示,其最小检出量为2.3×103cfu/mL;应用该法对10只RA病鸭的组织样品检测显示,脑组织检出率最高,其次为心血、肝脏和脾,而肠和肌肉呈阴性。同时,PCR法对RA的检出率比细菌分离鉴定法高11.7%。本研究建立的基于16S rRNA基因序列的PCR检测方法,能够检测主要流行于浙江地区的4种血清型RA,具有特异、灵敏和快速的优点。To establish a rapid diagnostic approach of Riemerella anatipestifer disease, the PCR assay was developed for detection of R.anatipestifer with a pair of primers designed according to the conserved region of 16S rRNA sequence of R.anatipestifer ATCC 11845 strain (Acc. No: CP003388.1) in NCBI. The results indicated that a 698 bp specific DNA fragment was able to be amplified from both standard R.anatipestifer strains (including serotype of 1, 2, 10 and 11) and clinical samples with a detection limit of 2.3x103 cfu/mL, but unable to be amplified from E.coli and Salmonella isolates. In addition, Different tissues collected from R.anatipestifer infected ducks were tested by the PCR assay, the results showed that the highest R.anatipestifer detection rate was from cerebral tissue, followed by heart blood, then liver and the spleen, but not detected from intestine and muscle. While, compared with bacterial isolation method, detection rate by PCR assay was 11.7% higher. These results indicated that the PCR assay based on 16S rRNA gene is specific, sensitive and rapid for detection of different serotype R.anatipestifer infection in ducks.
分 类 号:S852.61[农业科学—基础兽医学]
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在链接到云南高校图书馆文献保障联盟下载...
云南高校图书馆联盟文献共享服务平台 版权所有©
您的IP:216.73.216.3