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首页> 外文期刊>Biological Control: Theory and Application in Pest Management >Microsatellite markers to monitor a commercialized isolate of the entomopathogenic fungus Beauveria bassiana in different environments: technical validation and first applications.
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Microsatellite markers to monitor a commercialized isolate of the entomopathogenic fungus Beauveria bassiana in different environments: technical validation and first applications.

机译:微卫星标记,可在不同环境中监测昆虫致病性球孢白僵菌的商业分离株:技术验证和首次应用。

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摘要

Here, we report on the application of five previously developed microsatellite markers (simple sequence repeats, SSRs) to monitor an isolate of the entomopathogenic fungus Beauveria bassiana (Bals.) Vuill. in different environments. Discriminatory power of these SSR markers was assessed in two commercialized B. bassiana isolates as well as in 16 B. bassiana isolates from a world-wide collection, and three of the five SSR markers were estimated to allow a confident discrimination among the given isolates. Sensitivity thresholds of 0.1 pg DNA were subsequently determined for all SSR markers in case pure genomic fungal B. bassiana DNA was used as a template for PCR assays, but threshold levels varied depending on the environment (soil, plant) of the PCR assay. Furthermore, presence of a commercialized B. bassiana isolate was monitored via these SSR markers in three different types of potting substrates over a period of 14 weeks. With two SSR markers, strain-specific products were detected up to 14 weeks after application of B. bassiana to the substrate. Infectivity of B. bassiana conidia in the respective soil samples was confirmed by the Galleria baiting technique. Together these results indicate that molecular markers like SSRs specific for commercialized strains of entomopathogenic fungi are important tools to monitor a particular fungal strain in complex environmental samples such as bulk soil or plant DNA.
机译:在这里,我们报告五个以前开发的微卫星标记(简单的序列重复,SSR)的应用,以监测昆虫致病性真菌球孢白僵菌(巴尔)Vuill的分离。在不同的环境中。在两个商业化的球孢杆菌分离株以及全球范围内的16个球芽孢杆菌分离株中评估了这些SSR标记的鉴别力,据估计,五个SSR标记中的三个可以对给定的分离株进行可靠的区分。如果将纯基因组真菌球孢布鲁氏菌DNA用作PCR分析的模板,则随后针对所有SSR标记确定0.1 pg DNA的敏感性阈值,但阈值水平会因PCR分析的环境(土壤,植物)而异。此外,在14周的时间内,通过这些SSR标记在三种不同类型的盆栽基质中监测了商业化的球孢杆菌分离株的存在。使用两个SSR标记,在将球孢杆菌(B. bassiana)应用于底物后的14周内检测到菌株特异性产物。通过Galleria诱饵技术证实了球孢白僵菌分生孢子在各个土壤样品中的感染性。这些结果共同表明,对昆虫病原真菌商品化菌株具有特异性的分子标记(如SSR)是监测复杂环境样品(例如散装土壤或植物DNA)中特定真菌菌株的重要工具。

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