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锦鲤疱疹病毒TaqMan荧光定量PCR快速检测方法的建立及应用

孟庆峰 吕文雪 单晓枫 陈东升 王伟利 钱爱东

吉林农业大学学报2012,Vol.34Issue(3):339-342,354,5.
吉林农业大学学报2012,Vol.34Issue(3):339-342,354,5.

锦鲤疱疹病毒TaqMan荧光定量PCR快速检测方法的建立及应用

Establishment and Application of the TaqMan Real-Time PCR Detection Assay for Koi Herpesvirus

孟庆峰 1吕文雪 2单晓枫 1陈东升 1王伟利 3钱爱东2

作者信息

  • 1. 吉林农业大学动物科技学院,长春130118
  • 2. 吉林出入境检验检疫局,长春130062
  • 3. 东丰县畜牧总站,东丰136300
  • 折叠

摘要

Abstract

To establish a rapid and effective quarantine method of the Kio Hepesvinis disease, a set of primers and TaqMan probe for Fluorescent Quantitation PCR were designed to detect the conservative sequence of Kio Hepesvirus Sph genes. The cell cultures were detected by using the established quantitative PCR assay, and the results were compared with those of the routine PCR. The quantitative PCR sensitivity was higher than that of the routine PCR. The quantity of KHV DNA was 1.6×102 copies/μL. A reliable diagnostic result can be obtained just within 4 h. The assay proved to be a rapid, sensitive, specific and repetitive method for rapid detection of Kio Hepesvirus from fish in quarantine.

关键词

锦鲤疱疹病毒/荧光定量PCR/检测

Key words

koi herpesvirus/flurogenic quantitative polymerase chain reaction/detection

分类

农业科技

引用本文复制引用

孟庆峰,吕文雪,单晓枫,陈东升,王伟利,钱爱东..锦鲤疱疹病毒TaqMan荧光定量PCR快速检测方法的建立及应用[J].吉林农业大学学报,2012,34(3):339-342,354,5.

基金项目

吉林省科技发展计划项目(20080218) (20080218)