RWTH Aachen University, Institute for Biology I, Unit of Plant Molecular Cell Biology, Worringerweg 1, 52056 Aachen, Germany.
RWTH Aachen University, Institute for Biology III, Worringerweg 1, 52056 Aachen, Germany.
Mol Plant Microbe Interact. 2020 Aug;33(8):1008-1021. doi: 10.1094/MPMI-02-20-0035-TA. Epub 2020 Jun 29.
Powdery mildews are obligate biotrophic fungal pathogens causing important diseases of plants worldwide. Very little is known about the requirements for their pathogenicity at the molecular level. This is largely due to the inability to culture these organisms in vitro or to modify them genetically. Here, we describe a mutagenesis procedure based on ultraviolet (UV) irradiation to accumulate mutations in the haploid genome of the barley powdery mildew pathogen f. sp. . Exposure of f. sp. conidia to different durations of UV-C radiation (10 s to 12 min) resulted in a reduced number of macroscopically visible fungal colonies. f. sp. colony number was negatively correlated with exposure time and the total number of consecutive cycles of UV irradiation. Dark incubation following UV exposure further reduced fungal viability, implying that photoreactivation is an important component of DNA repair in f. sp. . After several rounds of UV mutagenesis, we selected two mutant isolates in addition to the parental f. sp. K1 isolate for whole-genome resequencing. By combining automated prediction of sequence variants and their manual validation, we identified unique UV-induced mutations in the genomes of the two isolates. Most of these mutations were in the up- or downstream regions of genes or in the intergenic space. Some of the variants detected in genes led to predicted missense mutations. As an additional insight, our bioinformatic analyses revealed a complex population structure within supposedly clonal f. sp. isolates.
白粉菌是专性活体营养真菌病原体,导致全球范围内的植物发生重要病害。对于它们在分子水平上的致病性的要求,人们知之甚少。这在很大程度上是由于无法在体外培养这些生物体或对其进行基因修饰。在这里,我们描述了一种基于紫外线(UV)照射的诱变程序,以在大麦白粉菌病原体 f. sp. 的单倍体基因组中积累突变。将 f. sp. 分生孢子暴露于不同时间的 UV-C 辐射(10 秒至 12 分钟)会导致肉眼可见的真菌菌落数量减少。f. sp. 菌落数量与暴露时间和连续 UV 照射的总循环数呈负相关。UV 照射后的暗培养进一步降低了真菌的活力,这意味着光复活是 f. sp. 中 DNA 修复的重要组成部分。经过几轮 UV 诱变,我们除了选择亲本 f. sp. K1 分离物之外,还选择了两个突变体分离物进行全基因组重测序。通过自动预测序列变体及其手动验证相结合,我们在两个分离物的基因组中鉴定出了独特的 UV 诱导突变。这些突变大多数位于基因的上下游区域或基因间空间。在检测到的一些基因变体导致了预测的错义突变。作为一个额外的见解,我们的生物信息学分析揭示了在假定的无性系 f. sp. 分离物中存在复杂的种群结构。