Romero M P, Wise K A
Department of Botany and Plant Pathology, Purdue University, West Lafayette, IN 47907.
Plant Dis. 2015 Jun;99(6):761-769. doi: 10.1094/PDIS-09-14-0917-RE. Epub 2015 Jun 11.
The causal agents of Diplodia ear rot are two species of the Stenocarpella genus, S. macrospora and S. maydis. In addition to ears, both pathogens can infect leaves and stalks, and both are present in most corn-production regions around the world. It is difficult to visually distinguish between the two pathogens based on plant symptoms and fungal signs. To facilitate accurate and rapid pathogen identification, polymerase chain reaction (PCR) assays were developed for identification of each species. Species-specific primers of 18 to 20 nucleotides in length were designed, targeting a portion of the internal transcribed spacer (ITS) region of the fungal genome for conventional and real-time PCR assays. The conventional PCR method successfully amplified a single 1.7-kb and 800-bp fragment for each S. maydis and S. macrospora isolate, respectively. The real-time method was performed using SYBR green dye, and detection of each specific target pathogen was successfully obtained. In total, 82 S. maydis and 15 S. macrospora isolates were tested to evaluate the reproducibility of these primers. Both methods provide a rapid and specific tool for the detection of Stenocarpella spp.
Diplodia穗腐病的病原菌是 Stenocarpella 属的两个物种,即大孢 Stenocarpella macrospora 和玉蜀黍 Stenocarpella maydis。除了玉米穗外,这两种病原菌都能感染叶片和茎秆,且在世界上大多数玉米产区都有存在。基于植物症状和真菌特征,很难从视觉上区分这两种病原菌。为了便于准确快速地鉴定病原菌,已开发出聚合酶链反应(PCR)检测方法来鉴定每个物种。设计了长度为18至20个核苷酸的物种特异性引物,靶向真菌基因组内部转录间隔区(ITS)的一部分用于常规PCR和实时PCR检测。常规PCR方法分别成功地为每个玉蜀黍 Stenocarpella maydis 和大孢 Stenocarpella macrospora 分离株扩增出一个1.7 kb和800 bp的片段。实时PCR方法使用SYBR绿染料进行,成功检测到了每个特定的目标病原菌。总共对82个玉蜀黍 Stenocarpella maydis 和15个大孢 Stenocarpella macrospora 分离株进行了测试,以评估这些引物的重复性。这两种方法都为 Stenocarpella 属病原菌的检测提供了一种快速且特异的工具。