Trout C L, Ristaino J B, Madritch M, Wangsomboondee T
Department of Plant Pathology, North Caro-lina State University, Raleigh 27695.
Plant Dis. 1997 Sep;81(9):1042-1048. doi: 10.1094/PDIS.1997.81.9.1042.
Late blight caused by the oomycete pathogen Phytophthora infestans is a devastating disease of potato and tomato worldwide. A rapid and accurate method for specific detection of P. infestans is necessary for determination of late blight in infected fruit, leaves, and tubers. Ribosomal DNA (rDNA) from four isolates of P. infestans representing the four genotypes US1, US6, US7, and US8 was amplified using polymerase chain reaction (PCR) and the universal primers internal transcribed spacer (ITS) 4 and ITS5. PCR products were sequenced using an automated sequencer. Sequences were aligned with published sequences from 5 other Phytophthora species, and a region specific to P. infestans was used to construct a PCR primer (PINF). Over 140 isolates representing 14 species of Phytophthora and at least 13 other genera of fungi and bacteria were used to screen the PINF primer. PCR amplification with primers PINF and ITS5 results in amplification of an approximately 600 base pair product with only isolates of P. infestans from potato and tomato, as well as isolates of P. mirabilis and P. cactorum. P. mirabilis and P. cactorum are not pathogens of potato; however, P. cactorum is a pathogen of tomato. P. infestans and P. cactorum were differentiated by restriction digests of the amplified product. The PINF primer was used with a rapid NaOH lysis technique for direct PCR of P. infestans from infected tomato and potato field samples. The PINF primer will provide a valuable tool for detection of P. infestans in potatoes and tomatoes.
由卵菌病原体致病疫霉引起的晚疫病是全球马铃薯和番茄的毁灭性病害。对于检测受感染果实、叶片和块茎中的晚疫病而言,一种快速准确的致病疫霉特异性检测方法必不可少。使用聚合酶链反应(PCR)和通用引物内转录间隔区(ITS)4和ITS5对代表美国1、美国6、美国7和美国8这四种基因型的四个致病疫霉分离株的核糖体DNA(rDNA)进行扩增。PCR产物使用自动测序仪进行测序。将序列与来自其他5种疫霉属物种的已发表序列进行比对,并使用致病疫霉特有的一个区域构建PCR引物(PINF)。使用代表14种疫霉属物种以及至少13个其他真菌和细菌属的140多个分离株来筛选PINF引物。使用引物PINF和ITS5进行PCR扩增时,仅来自马铃薯和番茄的致病疫霉分离株以及奇异疫霉和恶疫霉分离株会扩增出一个约600碱基对的产物。奇异疫霉和恶疫霉不是马铃薯的病原体;然而,恶疫霉是番茄的病原体。通过对扩增产物进行限制性酶切消化来区分致病疫霉和恶疫霉。PINF引物与快速NaOH裂解技术一起用于对来自受感染番茄和马铃薯田间样本的致病疫霉进行直接PCR。PINF引物将为检测马铃薯和番茄中的致病疫霉提供一个有价值的工具。