Real-time PCR for detection and quantification of fungal and oomycete tomato pathogens in plant and soil samples

被引:175
作者
Lievens, Bart
Brouwer, Margreet
Vanachter, Alfons C. R. C.
Cammue, Bruno P. A.
Thomma, Bart P. H. J.
机构
[1] Univ Wageningen & Res Ctr, Phytopathol Lab, NL-6709 PD Wageningen, Netherlands
[2] Katholieke Univ Leuven, CMPG, B-3001 Heverlee, Belgium
[3] Scientia Terrae Res Inst, B-2860 St Katelijne Waver, Belgium
关键词
Fusarium solani; internal transcribed spacer (ITS); Pythium ultimum; Rhizoctonia solani; SYBR Green I; Verticillium;
D O I
10.1016/j.plantsci.2006.03.009
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Although new, rapid detection and identification technologies are becoming available more and more for various plant pathogens, pathogen quantification remains one of the main challenges in the disease management of many crops. Currently, real-time polymerase chain reaction (PCR) is the most straightforward technique to quantify pathogen presence. This manuscript describes the use of real-time PCR to quantitatively assess the presence of a number of economically important fungal and oomycete tomato pathogens in biological samples. We demonstrate that pathogen DNA can be accurately quantified over at least four orders of magnitude. Additionally, we demonstrate the feasibility of the technique to quantify pathogen biomass in complex biological samples. (c) 2006 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:155 / 165
页数:11
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