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Development and use of new sensitive molecular tools for diagnosis and detection of Melampsora rusts on cultivated poplar

机译:新的敏感分子工具的开发和使用,用于诊断和检测栽培杨树上的Melampsora铁锈

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Poplar rusts due to Melampsora larici-populina (Mlp), M.allii-populina (Map) and M.medusae f. sp. deltoidae (Mmd) are the most serious disease in Europe on cultivated poplars, that is, Populusxeuramericana and P.xinteramericana hybrids. These pathogenic species can be identified by the observation of morphological characteristics of urediniospores but this method is not appropriate for high-throughput analysis and cannot be used on other spore stages, such as aeciospores or teliospores, that are morphologically similar. The aim of this study was to develop a rapid and sensitive molecular method based on PCR amplification that was able to specifically detect these species on various hosts for routine analysis. Three primer pairs ITS-MLP-F/ITS-MLP-R, ITS-MAP-F/ITS-MAP-R and ITS-MMD-F/ITS-MMD-R were designed within the internal transcribed spacer (ITS) sequences of ribosomal DNA to target Mlp, Map and Mmd, respectively, and their specificity were confirmed on a wide range of isolates and species. ITS-MLP-F/ITS-MLP-R and ITS-MAP-F/ITS-MAP-R primers proved to be highly specific to Mlp and Map, respectively, whereas ITS-MMD-F/ITS-MMD-R cross-reacted with DNA from M.larici-tremulae and M.pinitorqua. However, these species are not pathogenic on cultivated poplars that all belong to sections Aigeiros and Tacamahaca of the genus Populus. Specific Mmd primers proved to be very sensitive as a positive signal could be obtained with DNA extracts from 6 target urediniospores mixed with 800000 urediniospores of Mlp. An internal amplification control (IAC) was included to discriminate false negative results due to the potential presence of inhibitory compounds in DNA extracts. ITS-MMD-F/ITS-MMD-R primers are therefore efficient for the detection of the quarantine pathogen Mmd on samples collected on poplar or larch and are fit for use in official tests. This new PCR assay has been used in routine for ten years, and Mmd has hitherto never been detected in commercial poplar nurseries in France.RI Frey, Pascal/F-9212-2013; Husson, Claude/C-6113-2012OI Husson, Claude/0000-0002-9148-9926
机译:杨树锈病是由于Melampsora larici-populina(Mlp),M.allii-populina(Map)和M.medusae f。 sp。 deltoidae(Mmd)是欧洲栽培杨树上最严重的疾病,即Populusxeuramericana和P.xinteramericana杂种。这些病原体可以通过观察雷公子孢子的形态特征来识别,但是这种方法不适用于高通量分析,并且不能用于形态相似的其他孢子阶段,例如异孢子或孢子。这项研究的目的是开发一种基于PCR扩增的快速灵敏的分子方法,该方法能够在各种宿主上特异性检测这些物种以进行常规分析。在内部转录间隔区(ITS)序列中设计了三个引物对ITS-MLP-F / ITS-MLP-R,ITS-MAP-F / ITS-MAP-R和ITS-MMD-F / ITS-MMD-R分别针对Mlp,Map和Mmd的核糖体DNA及其特异性在多种分离物和物种中得到证实。 ITS-MLP-F / ITS-MLP-R和ITS-MAP-F / ITS-MAP-R引物分别对Mlp和Map具有高度特异性,而ITS-MMD-F / ITS-MMD-R交叉引物与M.larici-tremulae和M.pinitorqua的DNA反应。然而,这些物种对全部属于杨属的Aigeiros和Tacamahaca的栽培杨树没有致病性。事实证明,特定的Mmd引物非常敏感,因为可以从6个目标ursiosiospores的DNA提取物中混合800000的Mlp ursiosiospores获得阳性信号。由于DNA提取物中可能存在抑制性化合物,因此还包括一个内部扩增对照(IAC)以区分假阴性结果。因此,ITS-MMD-F / ITS-MMD-R引物可有效检测杨树​​或落叶松采集的样本上的检疫病原体Mmd,适合用于正式测试。这项新的PCR检测方法已在常规方法中使用了十年,迄今为止,在法国的商业杨树苗圃中从未发现过Mmd。RIFrey,Pascal / F-9212-2013;克劳德·休森/ C-6113-2012OI克劳德·休森/ 0000-0002-9148-9926

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