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试验土壤中烟草青枯病菌的RT-qPCR检测分析

程承 李石力 刘颖 王瑢笙 丁伟 张永强

烟草科技2017,Vol.50Issue(1):12-16,5.
烟草科技2017,Vol.50Issue(1):12-16,5.DOI:10.16135/j.issn1002-0861.2015.0668

试验土壤中烟草青枯病菌的RT-qPCR检测分析

RT-qPCR detection and quantitative analysis of Ralstonia solanacearum in soil

程承 1李石力 1刘颖 1王瑢笙 1丁伟 1张永强1

作者信息

  • 1. 西南大学植物保护学院,重庆市北碚区天生路2号 400716
  • 折叠

摘要

Abstract

To effectively control tobacco bacterial wilt, real-time quantitative PCR (RT-qPCR) technique was developed and used to quantitatively detect Ralstonia solanacearum in soil. The results showed that the lowest concentration of Ralstonia solanacearum in soil detected by the developed system was 5 × 102 cfu/g. Comparing with conventional PCR detection, the sensitivity of RT-qPCR detection to Ralstonia solanacearum in soil increased by 10 times.

关键词

烟草/青枯病/土壤/青枯雷尔氏菌/RT-qPCR

Key words

Tobacco/Bacterial wilt/Soil/Ralstonia solanacearum/Real-time quantitative PCR

分类

农业科技

引用本文复制引用

程承,李石力,刘颖,王瑢笙,丁伟,张永强..试验土壤中烟草青枯病菌的RT-qPCR检测分析[J].烟草科技,2017,50(1):12-16,5.

基金项目

国家烟草专卖局重点科技项目“茄青枯病菌与烟草互作分子机制及其调控技术研究”(110201202002)。 ()

烟草科技

OA北大核心CSCDCSTPCD

1002-0861

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