Department of Cell and Systems Biology, University of Toronto, Ontario, Canada.
Centre for the Analysis of Genome Evolution & Function, University of Toronto, Ontario, Canada.
Mol Plant Microbe Interact. 2020 Mar;33(3):394-401. doi: 10.1094/MPMI-10-19-0295-TA. Epub 2020 Jan 23.
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, nondestructive seedling pathology assay, and apply it to identify effector-triggered immunity (ETI) responses against 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 in . 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.
了解生物多样性如何影响植物-微生物相互作用变得越来越重要,特别是在病原体效应子库和植物免疫系统的成分方面。尽管技术进步极大地提高了我们检查分子序列和相互作用的能力,但很少有进展能够促进高通量、体内病理学筛选。在这里,我们提出了一种高通量、基于微孔板的、非破坏性的幼苗病理学测定方法,并将其应用于鉴定针对 III 型分泌效应子的效应子触发免疫(ETI)反应。该测定在 48 孔微孔板格式中进行喷雾接种,以半自动方式定量记录疾病症状,从而大大减少了时间和成本。该测定仅需要对常见实验室器皿进行微小修改,并且不使用专有软件。我们通过重现由 在 中诱导的已知 ETI 反应验证了该测定。我们还证明,我们可以定量区分来自同一微孔板中生长的各种植物基因型的反应。最后,我们表明,我们测定方法的结果可用于进行全基因组关联研究,以鉴定宿主免疫基因,重现用成熟植物独立获得的结果。