SCAR-based real time PCR to identify a biocontrol strain (T1) of Trichoderma atroviride and study its population dynamics in soils

被引:49
作者
Cordier, Christelle
Edel-Hermann, Veronique
Martin-Laurent, Fabrice
Blal, Bachar
Steinberg, Christian
Alabouvette, Claude
机构
[1] Agrauxine, F-29561 Quimper 09, France
[2] Univ Bourgogne, INRA, CMSE, UMR Microbiol & Geochim Sols, F-21065 Dijon, France
[3] Serv Sequencage & Genotypage, F-21065 Dijon, France
关键词
population dynamics; real-time PCR; SCAR; soils; Trichoderma;
D O I
10.1016/j.mimet.2006.06.006
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Strains of Trichoderma spp. are known for their antagonistic properties against plant pathogens, some are already on the market, others are under development. In order to launch a strain on the market its perfect identification at the species and strain levels is needed. The aim of this study is to (i) design a SCAR marker for specific identification of strain T1 of Trichoderma atroviride and (ii) monitor population dynamics of this strain in soil by real time PCR. A primer pair targeting a 141-bp fragment enabled specific detection of this strain without cross detection of autochthonous populations of Trichoderma in several field soils. In two soils, population dynamics assessed by real time PCR and the soil plate technique gave similar results. The molecular tools developed in this study satisfy the requirement for specific identification of the biocontrol strain and for detection and quantification of T. atroviride T1 population in complex environments. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:60 / 68
页数:9
相关论文
共 35 条
[1]  
Abbasi PA, 1999, APPL ENVIRON MICROB, V65, P5421
[2]   RHIZOSPHERE COMPETENCE OF BENOMYL-TOLERANT MUTANTS OF TRICHODERMA SPP [J].
AHMAD, JS ;
BAKER, R .
CANADIAN JOURNAL OF MICROBIOLOGY, 1988, 34 (05) :694-696
[3]   Cotransformation of Trichoderma harzianum with β-glucuronidase and green fluorescent protein genes provides a useful tool for monitoring fungal growth and activity in natural soils [J].
Bae, YS ;
Knudsen, GR .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2000, 66 (02) :810-815
[4]   A duplex-PCR bioassay to detect a Trichoderma virens biocontrol isolate in non-sterile soil [J].
Dodd, SL ;
Hill, RA ;
Stewart, A .
SOIL BIOLOGY & BIOCHEMISTRY, 2004, 36 (12) :1955-1965
[5]   Terminal restriction fragment length polymorphism analysis of ribosomal RNA genes to assess changes in fungal community structure in soils [J].
Edel-Hermann, W ;
Dreumont, C ;
Pérez-Piqueres, A ;
Steinberg, C .
FEMS MICROBIOLOGY ECOLOGY, 2004, 47 (03) :397-404
[6]   Biological control of foliar pathogens by means of Trichoderma harzianum and potential modes of action [J].
Elad, Y .
CROP PROTECTION, 2000, 19 (8-10) :709-714
[7]   Direct quantification of fungal DNA from soil substrate using real-time PCR [J].
Filion, M ;
St-Arnaud, M ;
Jabaji-Hare, SH .
JOURNAL OF MICROBIOLOGICAL METHODS, 2003, 53 (01) :67-76
[8]  
GOLDMAN GH, 1998, BASIC BIOL TAXONOMY, V1, P209
[9]   A TOOL FOR MONITORING TRICHODERMA-HARZIANUM .2. THE USE OF A GUS TRANSFORMANT FOR ECOLOGICAL-STUDIES IN THE RHIZOSPHERE [J].
GREEN, H ;
JENSEN, DF .
PHYTOPATHOLOGY, 1995, 85 (11) :1436-1440
[10]   Trichoderma species -: Opportunistic, avirulent plant symbionts [J].
Harman, GE ;
Howell, CR ;
Viterbo, A ;
Chet, I ;
Lorito, M .
NATURE REVIEWS MICROBIOLOGY, 2004, 2 (01) :43-56