CEPLAS, Institute for Plant Sciences, University of Cologne, Cologne, Germany.
IMPRS, Max Planck Institute for Plant Breeding Research, Cologne, Germany.
Plant J. 2021 May;106(3):733-752. doi: 10.1111/tpj.15195. Epub 2021 Apr 3.
The biotrophic pathogen Ustilago maydis causes smut disease on maize (Zea mays) and induces the formation of tumours on all aerial parts of the plant. Unlike in other biotrophic interactions, no gene-for-gene interactions have been identified in the maize-U. maydis pathosystem. Thus, maize resistance to U. maydis is considered a polygenic, quantitative trait. Here, we study the molecular mechanisms of quantitative disease resistance (QDR) in maize, and how U. maydis interferes with its components. Based on quantitative scoring of disease symptoms in 26 maize lines, we performed an RNA sequencing (RNA-Seq) analysis of six U. maydis-infected maize lines of highly distinct resistance levels. The different maize lines showed specific responses of diverse cellular processes to U. maydis infection. For U. maydis, our analysis identified 406 genes being differentially expressed between maize lines, of which 102 encode predicted effector proteins. Based on this analysis, we generated U. maydis CRISPR/Cas9 knock-out mutants for selected candidate effector sets. After infections of different maize lines with the fungal mutants, RNA-Seq analysis identified effectors with quantitative, maize line-specific virulence functions, and revealed auxin-related processes as a possible target for one of them. Thus, we show that both transcriptional activity and virulence function of fungal effector genes are modified according to the infected maize line, providing insights into the molecular mechanisms underlying QDR in the maize-U. maydis interaction.
生物致病病原体玉米黑粉菌会引起玉米(Zea mays)的黑粉病,并在植物的所有气生部分诱导肿瘤的形成。与其他生物相互作用不同,在玉米-玉米黑粉菌发病系统中尚未鉴定出基因对基因相互作用。因此,玉米对玉米黑粉菌的抗性被认为是多基因、数量性状。在这里,我们研究了玉米中数量抗性(QDR)的分子机制,以及玉米黑粉菌如何干扰其组成部分。基于 26 个玉米品系中疾病症状的定量评分,我们对六种具有高度不同抗性水平的玉米黑粉菌感染玉米品系进行了 RNA 测序(RNA-Seq)分析。不同的玉米品系对玉米黑粉菌感染表现出不同的细胞过程的特定反应。对于玉米黑粉菌,我们的分析鉴定了 406 个在玉米品系之间差异表达的基因,其中 102 个编码预测的效应蛋白。基于此分析,我们针对选定的候选效应物集生成了玉米黑粉菌 CRISPR/Cas9 敲除突变体。在用真菌突变体感染不同的玉米品系后,RNA-Seq 分析鉴定了具有定量、玉米品系特异性毒力功能的效应物,并揭示了生长素相关过程可能是其中一种的靶标。因此,我们表明真菌效应基因的转录活性和毒力功能都根据感染的玉米品系进行了修饰,为玉米-玉米黑粉菌相互作用中 QDR 的分子机制提供了新的见解。