Liu J L, Li Y Z, Nan Z B
College of Pastoral Agriculture Science and Technology, Lanzhou University, State Key Laboratory of Grassland Agro-ecosystems, Lanzhou, China; College of Biological Sciences and Engineering, Beifang University of Nationalities, Yinchuan, China.
Lett Appl Microbiol. 2015 Apr;60(4):372-8. doi: 10.1111/lam.12381. Epub 2015 Feb 15.
Embellisia astragali is an important seedborne pathogenic fungus responsible for yellow stunt and root rot of standing milk vetch (Astragalus adsurgens). The current detection methods that are based on culture and morphological identification are time-consuming, laborious and not always reliable. A PCR-based diagnostic method was developed with the species-specific primer pairs AatpF and AatpR designed from the sequence of the plasma membrane ATPase gene of E. astragali. The specificity of the primers was verified by PCR analysis of DNA from three strains of E. astragali and 19 isolates of nontarget fungi from other genera. A single 135-bp amplicon was detected only from E. astragali isolates, and no cross-reactions were observed with any other tested isolates. The detection limit of this new method was 5 pg of template DNA. The specific primers enabled the detection of E. astragali from the seed of standing milk vetch. This species-specific PCR method provides quick, simple, powerful and reliable detection of E. astragali.
PCR-based detection is fast, convenient, precise and sensitive compared to the traditional methods of pathogen detection. This study develops the first PCR method for the detection of Embellisia astragali in standing milk vetch seeds. The species-specific primer set designed from the plasma membrane ATPase gene of E. astragali can detect the pathogen. This assay could be applied in the standing milk vetch seed industry.
黄芪埃里格孢是一种重要的种传致病真菌,可导致直立黄芪黄化矮缩和根腐病。目前基于培养和形态学鉴定的检测方法耗时、费力且并非总是可靠。利用从黄芪埃里格孢质膜ATP酶基因序列设计的物种特异性引物对AatpF和AatpR,开发了一种基于PCR的诊断方法。通过对来自三株黄芪埃里格孢菌株和19株来自其他属的非靶标真菌分离物的DNA进行PCR分析,验证了引物的特异性。仅从黄芪埃里格孢分离物中检测到一个135 bp的单一扩增子,与任何其他测试分离物均未观察到交叉反应。这种新方法的检测限为5 pg模板DNA。特异性引物能够从直立黄芪种子中检测出黄芪埃里格孢。这种物种特异性PCR方法为黄芪埃里格孢提供了快速、简单、强大且可靠的检测。
与传统的病原体检测方法相比,基于PCR的检测快速、方便、精确且灵敏。本研究开发了第一种用于检测直立黄芪种子中黄芪埃里格孢的PCR方法。从黄芪埃里格孢质膜ATP酶基因设计的物种特异性引物组能够检测该病原体。该检测方法可应用于直立黄芪种子产业。