1 Wageningen UR, Droevendaalsesteeg 1, Biointeractions and Plant Health, 6708 PB, Wageningen, The Netherlands.
2 Dutch National Plant Protection Organization, National Reference Centre, Geertjesweg 15, 6706 EA, Wageningen, The Netherlands.
Phytopathology. 2019 Jun;109(6):1043-1052. doi: 10.1094/PHYTO-01-19-0024-R. Epub 2019 May 10.
The obligate biotrophic chytrid species is the causal agent of potato wart disease. Currently, 39 pathotypes have been described based on their interaction with a differential set of potato varieties. Wart resistance and pathotyping is performed using bioassays in which etiolated tuber sprouts are inoculated. Here, we describe an alternative method in which aboveground plant parts are inoculated. Susceptible plants produced typical wart symptoms in developing but not in fully expanded aboveground organs. Colonization of the host by was verified by screening for resting spores by microscopy and by molecular techniques using TaqMan polymerase chain reaction and RNAseq analysis. When applied to resistant plants, none of these symptoms were detectable. Recognition of pathotypes by differentially resistant potato varieties was identical in axillary buds and the tuber-based bioassays. This suggests that resistance genes are expressed in both etiolated "belowground" sprouts and green aboveground organs. RNAseq analysis demonstrated that the symptomatic aboveground materials contain less contaminants compared with resting spores extracted from tuber-based assays. This reduced microbial contamination in the aboveground bioassay could be an important advantage to study this obligate biotrophic plant-pathogen interaction. Because wart resistance is active in both below- and aboveground organs, the aboveground bioassay can potentially speed up screening for resistance in potato breeding programs because it omits the requirement for tuber formation. In addition, possibilities arise to express effectors in potato leaves through agroinfiltration, thereby providing additional phenotyping tools for research and breeding. Copyright © 2019 The Author(s). This is an open access article distributed under the CC BY 4.0 International license .
专性生物营养型的壶菌物种是马铃薯疣病的病原体。目前,根据其与马铃薯品种的差异互作,已描述了 39 种致病型。通过对黄化块茎芽接种的生物测定来进行疣病抗性和致病型鉴定。在这里,我们描述了一种替代方法,即接种地上部分。易感植物在发育中的但未完全展开的地上器官中产生典型的疣症状。通过显微镜检查和使用 TaqMan 聚合酶链反应和 RNAseq 分析的分子技术筛选休眠孢子,验证了宿主被 定殖。当应用于抗性植物时,这些症状都无法检测到。不同抗性马铃薯品种对 的识别在腋芽和基于块茎的生物测定中是相同的。这表明,在黄化的“地下”芽和绿色地上器官中都表达了 抗性基因。RNAseq 分析表明,与从基于块茎的测定中提取的休眠孢子相比,有症状的地上材料中含有较少的污染物。与基于块茎的生物测定相比,地上生物测定中减少的微生物污染可能是研究这种专性生物营养植物-病原体相互作用的一个重要优势。由于疣病抗性在地下和地上器官中都有活性,因此地上生物测定可以潜在地加快马铃薯抗病性筛选,因为它不需要块茎形成。此外,通过农杆菌浸润在马铃薯叶片中表达 效应子,为研究和育种提供了额外的表型工具,从而为研究和育种提供了更多可能性。版权所有©2019 作者。这是一个在 CC BY 4.0 国际许可下发布的开放获取文章。