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Detection and characterization of fungal infections of Ammophila arenaria (marram grass) roots by denaturing gradient gel electrophoresis of specifically amplified 18s rDNA.

机译:通过变性梯度凝胶电泳对特异扩增的18s rDNA进行变性检测和鉴定沙门氏菌(marram grass)根的真菌感染。

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摘要

Marram grass (Ammophila arenaria L.), a sand-stabilizing plant species in coastal dune areas, is affected by a specific pathosystem thought to include both plant-pathogenic fungi and nematodes. To study the fungal component of this pathosystem, we developed a method for the cultivation-independent detection and characterization of fungi infecting plant roots based on denaturing gradient gel electrophoresis (DGGE) of specifically amplified DNA fragments coding for 18S rRNA (rDNA). A nested PCR strategy was employed to amplify a 569-bp region of the 18S rRNA gene, with the addition of a 36-bp GC clamp, from fungal isolates, from roots of test plants infected in the laboratory, and from field samples of marram grass roots from both healthy and degenerating stands from coastal dunes in The Netherlands. PCR products from fungal isolates were subjected to DGGE to examine the variation seen both between different fungal taxa and within a single species. DGGE of the 18S rDNA fragments could resolve species differences from fungi used in this study yet was unable to discriminate between strains of a single species. The 18S rRNA genes from 20 isolates of fungal species previously recovered from A. arenaria roots were cloned and partially sequenced to aid in the interpretation of DGGE data. DGGE patterns recovered from laboratory plants showed that this technique could reliably identify known plant-infecting fungi. Amplification products from field A. arenaria roots also were analyzed by DGGE, and the major bands were excised, reamplified, sequenced, and subjected to phylogenetic analysis. Some recovered 18S rDNA sequences allowed for phylogenetic placement to the genus level, whereas other sequences were not closely related to known fungal 18S rDNA sequences. The molecular data presented here reveal fungal diversity not detected in previous culture-based surveys.
机译:沿海沙丘地区的沙草植物-沙兰草(Ammophila arenaria L.)受一种特殊的病理系统影响,该系统被认为既包括植物病原真菌,也包括线虫。为了研究此病理系统的真菌成分,我们开发了一种方法,该方法基于变性梯度凝胶电泳(DGGE)特异性扩增的编码18S rRNA(rDNA)的DNA片段,独立于培养物检测和表征真菌感染植物的根。采用巢式PCR策略扩增18S rRNA基因的569-bp区域,并从真菌分离物,实验室感染的试验植物的根和马拉姆的野外样品中添加36-bp的GC钳来自荷兰沿海沙丘的健康和退化林分的草根。对来自真菌分离物的PCR产物进行DGGE处理,以检查在不同真菌类群之间以及单个物种内所见的变异。 18S rDNA片段的DGGE可以解决本研究中使用的真菌的物种差异,但无法区分单个物种的菌株。克隆了20种先前从沙曲霉根中回收的真菌物种分离株的18S rRNA基因,并对其进行了部分测序,以帮助解释DGGE数据。从实验室植物中回收的DGGE模式表明,该技术可以可靠地鉴定出已知的感染植物的真菌。还用DGGE分析了来自野豌豆根的扩增产物,并对主要条带进行了切割,扩增,测序并进行了系统发育分析。一些恢复的18S rDNA序列允许系统发育到属水平,而其他序列与已知的真菌18S rDNA序列并不紧密相关。此处提供的分子数据揭示了在以前的基于培养的调查中未发现的真菌多样性。

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