Business unit Biointeractions and Plant Health, Plant Research International, PO Box 69, 6700 AB Wageningen, The Netherlands.
Phytopathology. 2009 Dec;99(12):1377-86. doi: 10.1094/PHYTO-99-12-1377.
ABSTRACT Isolates of Stemphylium vesicarium causing brown spot of pear can be distinguished from nonpathogenic isolates of S. vesicarium from pear or from other hosts on the basis of distinctive amplified fragment length polymorphism fingerprinting profiles. DNA fragments specific for isolates pathogenic to pear were identified and a quantitative polymerase chain reaction (PCR) was developed on the sequence from one of these specific DNA loci. This TaqMan PCR has a high sensitivity with a dynamic range for reliable quantification between 1 ng and 100 fg of DNA. The method detected pear-pathogenic isolates of S. vesicarium originating from four different European countries and various regions within those countries. No cross-reaction was found with either the nonpathogenic isolates of S. vesicarium tested or isolates belonging to other Stemphylium spp. or related fungi. The pathogen was detected on leaves with brown-spot symptoms originating from six different locations in The Netherlands, Italy, and Spain. Pear-pathogenic S. vesicarium populations were monitored on crop residues in two Dutch orchards between October 2007 and October 2008. Brown spot had been observed at both orchards at the end of the growing season of 2007. In one location, pear-pathogenic S. vesicarium was detected only sporadically on crop residues and no brown-spot symptoms were observed on fruit in 2008. At the other location, a pathogenic population was found on fallen pear leaves and on other crop residues but this population decreased during winter. From the beginning of the growing season in 2008 onward, the pathogen population could not be detected and the disease incidence was only 0.6%. The TaqMan PCR will allow more detailed studies on epidemiology of brown spot and on the effect of disease control measures.
摘要 引起梨褐斑病的茎点霉(Stemphylium vesicarium)分离物可以根据独特的扩增片段长度多态性指纹图谱,与来自梨或其他宿主的非致病性茎点霉(S. vesicarium)分离物区分开来。鉴定出了针对梨致病菌的 DNA 片段,并针对这些特定 DNA 位点之一的序列开发了一种定量聚合酶链反应(PCR)。该 TaqMan PCR 具有很高的灵敏度,可靠定量的动态范围为 1 ng 至 100 fg DNA。该方法检测到来自四个不同欧洲国家和这些国家内不同地区的具有致病性的梨茎点霉(S. vesicarium)分离物。与测试的非致病性茎点霉(S. vesicarium)分离物或属于其他茎点霉属(Stemphylium spp.)或相关真菌的分离物均未发生交叉反应。该病原体在来自荷兰、意大利和西班牙的六个不同地点的具有褐斑病症状的叶片上被检测到。在 2007 年 10 月至 2008 年 10 月期间,在两个荷兰果园中监测了作物残体上的梨致病菌种群。在 2007 年生长季节结束时,两个果园均观察到褐斑病。在一个地点,仅在作物残体上偶然检测到梨致病菌茎点霉(S. vesicarium),并且 2008 年未在果实上观察到褐斑病症状。在另一个地点,在掉落的梨叶和其他作物残体上发现了一个致病菌种群,但该种群在冬季减少。从 2008 年开始的生长季节开始,无法检测到病原体种群,发病率仅为 0.6%。TaqMan PCR 将允许对褐斑病的流行病学以及对疾病控制措施的影响进行更详细的研究。