生物技术通报 ›› 2014, Vol. 0 ›› Issue (1): 147-150.

• 研究报告 • 上一篇    下一篇

香菇dsRNA 病毒LeV 的RT-PCR 检测

郭杰1,2,吴小平1   

  1. 1. 福建农林大学生命科学学院,福州 350002
    2. 三门峡农业科学研究院,三门峡 472000
  • 收稿日期:2013-09-23 出版日期:2014-01-23 发布日期:2014-01-23
  • 作者简介:郭杰,男,助理农艺师,硕士,研究方向: 食用菌病害;E-mail: gjfywx_2008@163.com
  • 基金资助:
    福建省科技厅自然科学基金项目(2013J01080)

RT-PCR Detection of dsRNA Virus LeV in Lentinula edodes

Guo Jie1,2, Wu Xiaoping1   

  1. 1. College of Life Science,Fujian Agriculture and Forestry University,Fuzhou 350002;
    2. Institute of SanMenxia Agriculture Science,Sanmenxia 472000
  • Received:2013-09-23 Published:2014-01-23 Online:2014-01-23

摘要: 香菇病毒HKB(Lentinula edodes mycovirus HKB,LeV)是一种具有潜隐性特点的真菌病毒,广泛存在于香菇菌株中。#br#为了快速、准确地检测出LeV,根据LeV 病毒基因组序列(AB.429556.2)的信息,设计合成一对引物,对25 个香菇菌株进行RTPCR#br#检测,在20 个香菇菌株中分别扩增出LeV 病毒基因组特有的条带,在5 个香菇菌株中未能扩增出条带。通过对25 个香菇菌#br#株进行dsRNA 提取检测,结果也表明不存在扩增片段的菌株提取不到dsRNA,存在扩增片段的菌株能够提取得到dsRNA。因此建#br#立的RT-PCR 方法可以快速检测到香菇dsRNA 病毒LeV,能够对香菇的质量检测提供技术支持。

关键词: dsRNA, 真菌病毒, RT-PCR, 香菇

Abstract: Lentinula edodes mycovirus HKB(LeV)is a fungal virus with the potential symptoms and exists widely in Lentinula edodes strains. In order to detect LeV from abundant strains rapidly and accurately, a pair of primers were designed according to the sequence of LeV (AB.429556.2)and amplified by RT-PCR method. In a total of 25 strains, 20 strains were positive for LeV and 5 strains were negative. The result of dsRNA extraction also showed dsRNA were obtained in the positive strains and the negative strains were not. In conclusion, the study proved that RT-PCR is a rapid and sensitive method for detection of LeV in Lentinula edodes strains and can attribute to the control of strains quality.

Key words: dsRNA, Mycovirus, RT-PCR, Lentinula edodes