Specific SCAR markers and multiplex real-time PCR for quantification of two Trichoderma biocontrol strains in environmental samples

被引:12
|
作者
Feng, Xin Mei [1 ]
Holmberg, Anna-Ida Johnsson [1 ]
Sundh, Ingvar [1 ]
Ricard, Thomas [2 ]
Melin, Petter [1 ]
机构
[1] Swedish Univ Agr Sci, Uppsala BioCtr, Dept Microbiol, S-75007 Uppsala, Sweden
[2] BINAB Bioinnovat AB, S-25467 Helsingborg, Sweden
关键词
Ascomycetes; Golf; Hypocrea parapilulifera; Hypocreales; Trichoderma atroviride; Trichoderma polysporum; PSEUDOMONAS-FLUORESCENS EPS62E; BIOLOGICAL-CONTROL AGENT; RHIZOCTONIA-SOLANI; QUANTITATIVE PCR; SELECTIVE MEDIUM; FIRE BLIGHT; SOIL; HARZIANUM; MECHANISMS; TECHNOLOGY;
D O I
10.1007/s10526-011-9365-7
中图分类号
Q96 [昆虫学];
学科分类号
摘要
Several strains from the genus Trichoderma (Ascomycetes, Hypocreales) are commercially used as biocontrol agents, e.g. in formulations containing the two Trichoderma strains IMI206039 (Hypocrea parapilulifera B.S. Lu, Druzhinina & Samuels) and IMI206040 (T. atroviride P. Karst). To quantify the presence of the two isolates after application, we developed primers for SCAR markers (Sequence-Characterised Amplified Region). In order to quantify both fungal strains simultaneously, we also designed fluorophore-labelled probes distinguishing the two strains, to be used in combination with the SCAR primers. In incubations of two different soils, artificially inoculated and maintained under controlled conditions, the quantification through amplification with the SCAR markers in qPCR and through colony-forming units from plate counting correlated well. Further tests of the markers on samples taken from a golf green treated with a product containing both strains indicated that the two biocontrol strains did not establish, either on the golf green or in the surrounding area.
引用
收藏
页码:903 / 913
页数:11
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