Real-time PCR assay to quantify Fusarium graminearum wild-type and recombinant mutant DNA in plant material

被引:19
作者
Dyer, Rex B. [1 ]
Kendra, David F. [1 ]
Brown, Daren W. [1 ]
机构
[1] USDA ARS, Natl Ctr Agr Utilizat Res, Washington, DC 20250 USA
关键词
Fusarium graminearian; fusarium head blight; plant pathogen; quantitative assay; real-time PCR; SYBR green; wheat scab;
D O I
10.1016/j.mimet.2006.05.011
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Fusarium graminearum (teleomorph, Gibberella zeae) is the predominant causal agent of Fusarium head blight (FHB) of wheat resulting in yearly losses through reduction in grain yield and quality and accumulation of fungal generated toxins in grain. Numerous fungal genes potentially involved in virulence have been identified and studies with deletion mutants to ascertain their role are in progress. Although wheat field trials with wild-type and mutant strains are critical to understand the role these genes may play in the disease process, the interpretation of field trial data is complicated by FHB generated by indigenous species of F graminearum. This report describes the development of a SYBR green-based real time PCR assay that quantifies the total F graminearum genomic DNA in a plant sample as well as the total F graminearum genomic DNA contributed from a strain containing a common fungal selectable marker used to create deletion mutants. We found our method more sensitive, reproducible and accurate than other similar recently described assays and comparable to the more expensive probe-based assays. This assay will allow investigators to correlate the amount of disease observed in wheat field trials to the E graminearum mutant strains being examined. Published by Elsevier B.V.
引用
收藏
页码:534 / 542
页数:9
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