Department of Plant Pathology and MOA Key Lab of Pest Monitoring and Green Management, College of Plant Protection, China Agricultural University, 100193, Beijing, China.
United States Department of Agriculture-Agricultural Research Service, San Joaquin Valley Agricultural Sciences Center, Parlier, CA 93648.
Plant Dis. 2018 Aug;102(8):1527-1533. doi: 10.1094/PDIS-10-17-1662-RE. Epub 2018 Jun 25.
Brown rot is a severe disease affecting stone and pome fruit. This disease was recently confirmed to be caused by the following six closely related species: Monilinia fructicola, M. laxa, M. fructigena, Monilia polystroma, M. mumecola, and M. yunnanensis. Because of differences in geographic distributions, some of these species are important quarantine pathogens in certain countries. In this study, we developed TaqMan real-time polymerase chain reaction (PCR) assays to detect and identify the six species. Primer pairs and probes were designed for Monilinia fructicola, M. fructigena, M. laxa, and Monilia polystroma based on sequence differences in the laccase-2 genes. Additionally, based on sequence differences in the elongation factor genes, primer pairs and probes were designed for Monilia mumecola and M. yunnanensis. The real-time PCR assays were able to specifically identify the target pathogens, with detection limits of 10 to 100 fg of DNA, which is equivalent to one to seven conidia. The assays were also able to detect the target pathogens in a mixed DNA sample comprising all six Monilinia spp. and related species. The real-time PCR assays accurately detected target fungi from infected apple fruit. Furthermore, the identification results were consistent with those of traditional morphological methods.
桃褐腐病是一种严重影响核果和梨果的病害。最近证实,该病害是由以下 6 个密切相关的种引起的:桃褐腐病菌、M. laxa、M. fructigena、M. polystroma、M. mumecola 和 M. yunnanensis。由于地理分布的差异,这些物种中的一些在某些国家是重要的检疫性病原菌。在本研究中,我们开发了 TaqMan 实时聚合酶链反应(PCR)检测方法,用于检测和鉴定这 6 个种。基于漆酶-2 基因序列差异,为桃褐腐病菌、M. fructigena、M. laxa 和 M. polystroma 设计了引物对和探针。此外,基于延伸因子基因的序列差异,为 M. mumecola 和 M. yunnanensis 设计了引物对和探针。实时 PCR 检测方法能够特异性识别目标病原菌,检测限为 10 至 100 fg DNA,相当于 1 至 7 个分生孢子。该检测方法还能够在包含所有 6 种 Monilinia spp. 和相关种的混合 DNA 样本中检测到目标病原菌。实时 PCR 检测方法能够准确地从感染的苹果果实中检测到目标真菌。此外,鉴定结果与传统形态学方法一致。