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首页> 外文期刊>Journal of applied microbiology >Quantitative Fusarium spp. and Microdochium spp. PCR assays to evaluate seed treatments for the control of Fusarium seedling blight of wheat
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Quantitative Fusarium spp. and Microdochium spp. PCR assays to evaluate seed treatments for the control of Fusarium seedling blight of wheat

机译:定量镰刀菌属。和Microdochium spp。 PCR试验评估种子处理对小麦枯萎病的控制作用

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Aims: To develop sensitive quantitative PCR assays for the two groups of pathogens responsible for Fusarium seedling blight in wheat: Fusarium group (Fusarium culmorum and Fusarium graminearum) and Microdochium group (Microdochium nivale and Microdochium majus); and to use the assays to assess performance of fungicide seed treatments against each group. Methods and Results: Primers conserved between the species within each group were used to develop competitive PCR assays and used to quantify DNA of each group in wheat seed produced from inoculated field plots. Seed was used in seed treatment efficacy field experiments and the amount of DNA of each group was determined in emerged seedlings. The performance of treatments towards each group of pathogens was evaluated by comparison of the reduction in DNA in seedlings emerged from treated seed compared with untreated seed. Conclusions: DNA from the two groups of pathogens causing Fusarium seedling blight of wheat can be quantified separately using the competitive PCR assays. These assays show improved sensitivity compared with those previously reported for the individual species and allowed the quantification of pathogen DNA in seed and seedlings. Significant reductions in pathogen DNA were evident for each seed treatment. Significance and Impact of the Study: Quantification of DNA for each group allows the evaluation of seed treatment performance towards the two components of Fusarium seedling blight disease complex. The approach taken and the assays developed in this study will be of use for the study of other Fusarium disease complexes and their control. Based on the results reported here on the seedling stage of crop development, further studies that examine the control of seed-borne pathogens through fungicide seed treatments throughout the growing season are warranted.
机译:目的:开发针对小麦中枯萎病的两类病原体的敏感定量PCR分析方法:镰刀菌组(Fusarium culmorum和镰孢镰刀菌Fusarium graminearum)和微d组(Microdochium)(Microdochium nivale和Microdochium majus);并使用这些分析方法评估针对每组的杀菌剂种子处理的效果。方法和结果:使用每组物种之间保守的引物进行竞争性PCR分析,并用于定量从接种田地中产生的小麦种子中每组的DNA。种子用于种子处理功效田间试验,并测定出苗中每组的DNA量。通过比较从处理过的种子和未处理过的种子中萌发的幼苗中DNA的减少来评估针对每一种病原体的处理性能。结论:使用竞争性PCR分析可以分别定量引起小麦枯萎病的两组病原体的DNA。与以前报道的单个物种相比,这些分析显示出更高的灵敏度,并且可以定量种子和幼苗中的病原体DNA。每种种子处理均明显减少了病原体DNA。研究的意义和影响:每组DNA的定量分析可以评估针对镰刀苗枯萎病复合物两个成分的种子处理性能。本研究中采用的方法和开发的测定方法将用于研究其他镰刀菌病复合物及其控制。根据此处报告的关于作物生长的幼苗阶段的结果,有必要进行进一步研究,以研究在整个生长季节通过杀菌剂种子处理对种子传播病原体的控制。

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