Max Planck Institute for Terrestrial Microbiology, Karl von Frisch Str., D-35043 Marburg, Germany.
New Phytol. 2011 Jan;189(2):471-83. doi: 10.1111/j.1469-8137.2010.03474.x. Epub 2010 Oct 11.
Infection of maize (Zea mays) plants with the corn smut fungus Ustilago maydis leads to the formation of large tumors on the stem, leaves and inflorescences. In this biotrophic interaction, plant defense responses are actively suppressed by the pathogen, and previous transcriptome analyses of infected maize plants showed massive and stage-specific changes in host gene expression during disease progression. To identify maize genes that are functionally involved in the interaction with U. maydis, we adapted a virus-induced gene silencing (VIGS) system based on the brome mosaic virus (BMV) for maize. Conditions were established that allowed successful U. maydis infection of BMV-preinfected maize plants. This set-up enabled quantification of VIGS and its impact on U. maydis infection using a quantitative real-time PCR (qRT-PCR)-based readout. In proof-of-principle experiments, an U. maydis-induced terpene synthase was shown to negatively regulate disease development while a protein involved in cell death inhibition was required for full virulence of U. maydis. The results suggest that this system is a versatile tool for the rapid identification of maize genes that determine compatibility with U. maydis.
玉米(Zea mays)植株感染玉蜀黍黑粉菌(Ustilago maydis)会导致其茎、叶和花序上形成大肿瘤。在这种生物共生关系中,病原体积极抑制植物防御反应,先前对感染玉米植株的转录组分析表明,在疾病进展过程中,宿主基因表达发生了大规模的、特定阶段的变化。为了鉴定与 U. maydis 互作的玉米功能基因,我们基于糜子黄花叶病毒(BMV)为玉米开发了一种病毒诱导的基因沉默(VIGS)系统。建立了使 BMV 预先感染的玉米植株成功感染 U. maydis 的条件。该方案允许使用基于定量实时 PCR(qRT-PCR)的读数来定量 VIGS 及其对 U. maydis 感染的影响。在原理验证实验中,证明了一种 U. maydis 诱导的萜烯合酶负调控疾病发展,而参与细胞死亡抑制的蛋白质是 U. maydis 完全毒力所必需的。结果表明,该系统是一种快速鉴定决定与 U. maydis 相容性的玉米基因的通用工具。