Murdoch University, Heath Science, Murdoch, WA 6150, Australia.
Mol Plant Pathol. 2012 Aug;13(6):531-45. doi: 10.1111/j.1364-3703.2011.00770.x. Epub 2011 Dec 6.
The wheat pathogen Stagonospora nodorum, causal organism of the wheat disease Stagonospora nodorum blotch, has emerged as a model for the Dothideomycetes, a large fungal taxon that includes many important plant pathogens. The initial annotation of the genome assembly included 16,586 nuclear gene models. These gene models were used to design a microarray that has been interrogated with labelled transcripts from six cDNA samples: four from infected wheat plants at time points spanning early infection to sporulation, and two time points taken from growth in artificial media. Positive signals of expression were obtained for 12,281 genes. This represents strong corroborative evidence of the validity of these gene models. Significantly differential expression between the various time points was observed. When infected samples were compared with axenic cultures, 2882 genes were expressed at a higher level in planta and 3630 were expressed more highly in vitro. Similar numbers were differentially expressed between different developmental stages. The earliest time points in planta were particularly enriched in differentially expressed genes. A disproportionate number of the early expressed gene products were predicted to be secreted, but otherwise had no obvious sequence homology to functionally characterized genes. These genes are candidate necrotrophic effectors. We have focused attention on genes for carbohydrate metabolism and the specific biosynthetic pathways active during growth in planta. The analysis points to a very dynamic adjustment of metabolism during infection. Functional analysis of a gene in the coenzyme A biosynthetic pathway showed that the enzyme was dispensable for growth, indicating that a precursor is supplied by the plant.
小麦条锈病菌(Stagonospora nodorum)是引起小麦条锈病的病原菌,它已成为一种模式生物,用于研究子囊菌门(Dothideomycetes),这是一个包含许多重要植物病原菌的真菌大类群。最初对基因组组装的注释包括 16586 个核基因模型。这些基因模型被用来设计微阵列,并用来自六个 cDNA 样本的标记转录本进行检测:四个样本来自感染小麦的时间点,涵盖了早期感染到孢子形成,另外两个时间点取自人工培养基中的生长。12281 个基因的表达得到了阳性信号。这为这些基因模型的有效性提供了强有力的佐证。在不同时间点观察到了显著的差异表达。当将感染样本与无菌培养物进行比较时,2882 个基因在植物体内表达水平更高,3630 个基因在体外表达水平更高。在不同发育阶段也观察到了类似数量的差异表达。植物体内的早期时间点尤其富含差异表达基因。早期表达的基因产物中有相当数量被预测为分泌蛋白,但与功能表征基因没有明显的序列同源性。这些基因是候选的坏死性效应子。我们关注了碳水化合物代谢和在植物体内生长过程中活跃的特定生物合成途径的基因。分析表明,在感染过程中,代谢发生了非常动态的调整。对辅酶 A 生物合成途径中的一个基因的功能分析表明,该酶的生长是可有可无的,这表明植物提供了前体物质。