Sap-direct RT-PCR for the rapid detection of coleus blumei viroids of the genus Coleviroid from natural host plants

被引:16
作者
Jiang, Dongmei [1 ,2 ]
Wu, Zujian [2 ]
Xie, Lianhui [2 ]
Sano, Teruo [3 ]
Li, Shifang [1 ]
机构
[1] Chinese Acad Agr Sci, Inst Plant Protect, State Key Lab Biol Plant Dis & Insect Pests, Beijing 100193, Peoples R China
[2] Fujian Agr & Forestry Univ, Inst Plant Virol, Fuzhou 350002, Fujian Province, Peoples R China
[3] Hirosaki Univ, Dept Plant Pathol, Fac Agr & Life Sci, Hirosaki, Aomori 0368561, Japan
基金
中国国家自然科学基金;
关键词
Sap; RT-PCR; Coleus; CbVd; Pipettor; SEQUENCE VARIANT; IN-VIVO; AMPLIFICATION; SEEDS;
D O I
10.1016/j.jviromet.2011.03.018
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A simple and fast sap-direct RT-PCR (reverse transcription-polymerase chain reaction) for the rapid detection of 3 viroids of the genus Coleviroid is presented. The templates for cDNA synthesis were obtained directly from the sap of coleus using a pipettor, a common tool in molecular biology laboratories, and 3 coleus blumei viroids (CbVds) were detected simultaneously using a pair of universal primers designed according to sequences in the central conserved region (CCR) of CbVds. RT-PCR results demonstrated that CbVd-1, CbVd-5, and CbVd-6 can be detected accurately in viroid-infected plants but not in viroid-free plants. The results of RT-PCR, dot-blot, sequencing, and batch-detection revealed that this method can be used to identify CbVds rapidly. The method also reduces cross-contamination among different samples to a minimum. It is considered that this rapid and simple technique is an effective method for the identification and cloning of CbVds. Crown Copyright (C) 2011 Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:123 / 127
页数:5
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