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:徐丽晶[1,2] 赵丽丽[2] 刘海燕[2] 王怡平 陈洪岩[1,2] XU Li-jing1,2, ZHAO Li-li2, LIU Hai-yan2, WANG Yi-ping2, CHEN Hong-yan1,2(1. College of Life Science, Northeast Agricultural University, Harbin 150030, China; 2. State Key Laboratory of Veterinary Biotechnology/Heilongjiang Provincial Key Laboratory of Laboratory Animal and Comparative Medicine/Harbin Veterinary Research Institute, Chinese A cademy of Agricultural Sciences ,Harbin 150069, Chin)
机构地区:[1]东北农业大学生命科学学院,黑龙江哈尔滨150030 [2]中国农业科学院哈尔滨兽医研究所,兽医生物技术国家重点实验室,黑龙江省实验动物与比较医学重点实验室,黑龙江哈尔滨150069
出 处:《中国兽医科学》2018年第4期456-463,共8页Chinese Veterinary Science
基 金:黑龙江省自然科学基金重点项目(ZD2016006);中央级公益性科研院所基本科研业务费专项(Y2016PT41);中央级公益性科研院所基本科研业务费专项(工作编号1610302016013和1610302017013)
摘 要:为了建立一种能同时检测I型鸭肝炎病毒(duck hepatitis virustype I,DHV—I)和鸭瘟病毒(duckplague virus,DPV)的检测方法,根据GrenBank中DHV-I和DPV的基因保守序列.设计合成两对特异性引物,扩增得到DHV—I和DPV片段,大小分别为399bp和232bp。据此建立了双重PCR检测方法,并将反应条件进行了优化。结果显示,该方法特异性强,能同时扩增出DHV—I和DPV目的条带,而对其他常见的水禽病病原的扩增结果均为阴性。该方法灵敏度高,最低能检出5.3PgI型鸭肝炎病毒和2.7pg鸭瘟病毒的RNA或DNA。采用该方法对在江苏省徐州地区所采集的166份鸭肛拭子进行检测,DHV—I阳性率为1.2%:DPV阳性率为26%。同时。利用该方法对建立的DHV—I和DPV雏鸭感染模型的肝组织和肝组织接种的鸭胚尿囊液进行检测,结果均为阳性.与常规PCR和RT—PCR检测结果一致。上述结果表明。本研究建立的一步法二重RT—PCR方法可以用于DHV—I和DPV快速准确的诊断。In order to establish a method for simultaneous detection of duck hepatitis virus type I (DHV-I)and duck plague virus(DPV),the one-step duplex PCR was established with 2 pairs of specific primers which were designed based on the conserved sequences of DHV- I and DPV, of which one was used for specifically amplification of a 399 bp fragment of DHV-I,and the other for amplification of a 232 bp fragment of DPV. The reaction conditions of the annealing temperature and the primer concentration were optimized. The one-step duplex PCR assay is specific and was able to simultaneously detect DHV- I and DPV and there were not specifically amplified for other common pathogenic for waterfowl diseases. Tem- plates of DHV- I and DPV were detected 5.3pg and 2. Tpg at a minimum which were proved to have high sensi- tivity. Furthermore,the established assay was used to detect the 166 clinical samples of duck anus swabs from Xuzhou,Jiangsu province. The results showed that the positive rates of DHV- I and DPV were 1.2% and 26%. Meanwhile, duck embryo allantoic fluid and liver tissues of DHV- I and DPV in duckling infection models were detected by this method and the results were positive in accord with that of the conventional PCR and RT-PCR results. The above-mentioned results indicated that the one-step duplex RT-PCR assay could be used for rapid and accurate diagnosis of DHV- I and DPV,simultaneously.
关 键 词:I型鸭肝炎病毒 鸭瘟病毒 一步法二重RT—PCR
分 类 号:S852.659.1[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:216.73.216.36