A PCR assay for the quantification of growth of the oomycete pathogen Hyaloperonospora arabidopsidis in Arabidopsis thaliana

被引:20
作者
Anderson, Ryan G. [1 ]
McDowell, John M. [1 ]
机构
[1] Virginia Tech, Dept Plant Pathol Physiol & Weed Sci, Blacksburg, VA 24061 USA
基金
美国国家科学基金会;
关键词
Arabidopsis; Hyaloperonospora arabidopsidis; oomycete; real-time PCR; DOWNY MILDEW; PERONOSPORA-PARASITICA; RESISTANCE; EDS1; GENES; EXPRESSION; INFECTION;
D O I
10.1111/mpp.12247
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
The accurate quantification of disease severity is important for the assessment of host-pathogen interactions in laboratory or field settings. The interaction between Arabidopsis thaliana and its naturally occurring downy mildew pathogen, Hyaloperonospora arabidopsidis (Hpa), is a widely used reference pathosystem for plant-oomycete interactions. Current methods for the assessment of disease severity in the Arabidopsis-Hpa interaction rely on measurements at the terminal stage of pathogen development; namely, visual counts of spore-producing structures or the quantification of spore production with a haemocytometer. These assays are useful, but do not offer sensitivity for the robust quantification of small changes in virulence or the accurate quantification of pathogen growth prior to the reproductive stage. Here, we describe a quantitative real-time polymerase chain reaction (qPCR) assay for the monitoring of Hpa growth inplanta. The protocol is rapid, inexpensive and can robustly distinguish small changes in virulence. We used this assay to investigate the dynamics of early Hpa mycelial growth and to demonstrate the proof of concept that this assay could be used in screens for novel oomycete growth inhibitors.
引用
收藏
页码:893 / 898
页数:6
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