Zahn Marc, Teuber Felix, Bollig Katharina, Horst Walter Johannes
Institute for Plant Nutrition, Faculty of Natural Sciences, Leibniz University Hannover, 30419 Hannover, Germany.
Plant Dis. 2011 Apr;95(4):394-400. doi: 10.1094/PDIS-07-10-0487.
Black leaf mold (BLM), caused by Pseudocercospora fuligena, is a major plant growth- and yield-limiting factor for tomato production in the humid tropics. A library of 90 introgession lines (ILs), the BLM-resistant donor Solanum habrochaites, and the BLM-susceptible recurrent S. lycopersicum parent (RP) were visually phenotyped under natural infection conditions in a nethouse in central Thailand. ILs showing no and severe BLM symptoms were among the phenotypes. Because visually classifying different phenotypes of BLM symptoms can lead to erroneous results due to the similarity of BLM symptoms to other abiotic and biotic problems, a SYBR Green-based quantitative polymerase chain reaction (qPCR) assay for fungal DNA was developed. Correlation of the results from visual phenotyping of plants grown in Thailand under natural infection conditions with qPCR test-based quantities of the tomato leaf fungal DNA content, while significant, explained only 39% of the relationship across the library population. Based on this phenotyping in Thailand, selected ILs were artificially infected in a growth chamber in Germany with a P. fuligena isolate from Thailand. The results of the natural infection could be verified for the selected ILs in the growth-chamber experiment. A close correlation (R = 0.87) existed between the visual disease rating and fungal DNA content in leaves in the latter experiment. Three lines without visual symptoms and very low amounts of P. fuligena-specific rDNA shared an overlapping introgression on chromosome one that may be associated with BLM resistance.
由番茄假尾孢菌引起的黑叶霉病(BLM)是潮湿热带地区番茄生产中限制植株生长和产量的主要因素。在泰国中部的一个网室自然感染条件下,对90个渗入系(ILs)文库、抗BLM的供体野生番茄以及感BLM的轮回亲本栽培番茄(RP)进行了表型观察。观察到的表型包括无BLM症状和有严重BLM症状的渗入系。由于BLM症状与其他非生物和生物问题相似,通过视觉对BLM症状的不同表型进行分类可能会导致错误结果,因此开发了一种基于SYBR Green的真菌DNA定量聚合酶链反应(qPCR)检测方法。在泰国自然感染条件下种植的植株的视觉表型分析结果与基于qPCR检测的番茄叶片真菌DNA含量之间的相关性虽然显著,但在整个文库群体中仅解释了39%的关系。基于在泰国的这种表型分析,从文库中挑选出的渗入系在德国的生长室中用来自泰国的番茄假尾孢菌分离株进行人工感染。在生长室实验中,所选渗入系的自然感染结果得到了验证。在后一个实验中,视觉病害评级与叶片中的真菌DNA含量之间存在密切相关性(R = 0.87)。三个无视觉症状且番茄假尾孢菌特异性rDNA含量极低的株系在1号染色体上有一个重叠的渗入片段,该片段可能与BLM抗性有关。