A High-Throughput, Seedling Screen for Plant Immunity

被引:6
|
作者
Martel, Alexandre [1 ]
Lo, Timothy [1 ]
Desveaux, Darrell [1 ,2 ]
Guttman, David S. [1 ,2 ]
机构
[1] Univ Toronto, Dept Cell & Syst Biol, Toronto, ON, Canada
[2] Univ Toronto, Ctr Anal Genome Evolut & Funct, Toronto, ON, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
Arabidopsis thaliana; avirulence factors; effectors; effector-triggered immunity (ETI); Pseudomonas syringae; resistance genes; screen; seedling; type III secreted effector (T3SE); type-3; secretion; GENOME-WIDE ASSOCIATION; PSEUDOMONAS-SYRINGAE; ARABIDOPSIS-THALIANA; EFFECTOR PROTEINS; RESISTANCE GENE; BACTERIAL; RECOGNITION; MUTATIONS; FAMILY; RPS2;
D O I
10.1094/MPMI-10-19-0295-TA
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
An understanding of how biological diversity affects plant-microbe interactions is becoming increasingly important, particularly with respect to components of the pathogen effector arsenal and the plant immune system. Although technological improvements have greatly advanced our ability to examine molecular sequences and interactions, relatively few advances have been made that facilitate high-throughput, in vivo pathology screens. Here, we present a high-throughput, microplate-based, non-destructive seedling pathology assay, and apply it to identify Arabidopsis thaliana effector-triggered immunity (ETI) responses against Pseudomonas syringae type III secreted effectors. The assay was carried out in a 48-well microplate format with spray inoculation, and disease symptoms were quantitatively recorded in a semiautomated manner, thereby greatly reducing both time and costs. The assay requires only slight modifications of common labware and uses no proprietary software. We validated the assay by recapitulating known ETI responses induced by P. syringae in Arabidopsis. We also demonstrated that we can quantitatively differentiate responses from a diversity of plant genotypes grown in the same microplate. Finally, we showed that the results obtained from our assay can be used to perform genome-wide association studies to identify host immunity genes, recapitulating results that have been independently obtained with mature plants.
引用
收藏
页码:394 / 401
页数:8
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