首页 | 本学科首页   官方微博 | 高级检索  
     

传染性支气管炎病毒实时荧光PCR检测方法的建立
引用本文:杜雄伟,李叶,张雪.传染性支气管炎病毒实时荧光PCR检测方法的建立[J].食品科学,2012,33(24):219-221.
作者姓名:杜雄伟  李叶  张雪
作者单位:西南大学化学化工学院,发光与实时分析教育部重点实验室,重庆 400715
基金项目:中央高校基本科研业务费专项(DC12010304)
摘    要:建立特异、敏感、快速的传染性支气管炎病毒(IBV)实时荧光定量PCR检测方法。针对IBV基因序列保守区域设计一对特异性引物和一条特异性的探针,建立实时荧光定量PCR检测方法,并进行特异性、敏感性、重复性检测。结果表明所建立的IBV实时荧光定量PCR检测方法,引物和探针特异性良好,组间组内重复性良好,检出IBV DNA最小拷贝数为5拷贝。因此,本研究建立IBV特异、敏感、快速的实时荧光PCR检测方法,为IBV的诊断奠定基础。

关 键 词:传染性支气管炎病毒  实时荧光PCR  
收稿时间:2011-12-23

Development of a Real-Time Fluorescent RT-PCR Assay for Detection of Infectious Bronchitis Virus
DU Xiong-wei,LI Ye,ZHANG Xue.Development of a Real-Time Fluorescent RT-PCR Assay for Detection of Infectious Bronchitis Virus[J].Food Science,2012,33(24):219-221.
Authors:DU Xiong-wei  LI Ye  ZHANG Xue
Affiliation:Key Laboratory on Luminescence and Real-Time Analysis, Ministry of Education,College of Chemistry and Chemical Engineering, Southwest University, Chongqing 400715, China
Abstract:A real-time PCR method was developed for the specific, sensitive and rapid detection of infectious bronchitis virus (IBV). A pair of specific primers and a specific probe were designed according to the IBV gene conserved sequence. The specificity, sensitivity and repeatability of this method were analyzed. This method was shown to have good specificity and repeatability and the minimum detection of IBV DNA copy number was 5. This RT-PCR assay showed high IBV specificity, sensitivity and time-saving and thus could provide a helpful tool for the prognosis of IBV.
Keywords:infectious bronchitis virus (IBV)  fluorescent RT-PCR  
本文献已被 CNKI 等数据库收录!
点击此处可从《食品科学》浏览原始摘要信息
点击此处可从《食品科学》下载全文
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