基于ITS的宏阵列与ITS群落探针的杂交用于真菌和真菌样原生生物复杂群落的表征

Antonio D. Izzo , Mark Mazzola
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引用次数: 13

摘要

表征环境中真菌群落结构和动态的能力不断受到必须面对的高水平多样性的挑战。目前正在开发用于这种分析研究的大规模寡核苷酸阵列;但是,执行这种方法通常需要大量的时间和财政资源。为了满足对真菌群落分析和广泛诊断的更容易获得的工具的需求,我们评估了反向点印迹方法的潜在效用,该方法利用macroarray靶点和探针,每个靶点和探针由整个真菌ITS1-5.8S-ITS2基因区域的PCR产物组成。用于生成阵列靶标的样品包括可培养和不可培养的真菌以及代表一系列生态功能的真菌样原生生物。使用单种探针在Pythium属内进行的测试表明,当ITS DNA序列相似性差异大于5 - 10%时,通常可以区分分类谱系。一个已知组成的人工构建的群落探针成功地检测了阵列中包含的10个谱系中的8个,在95个目标中只有一个明显的假阳性。该方法也成功地应用于环境样品。利用该阵列识别了当地果园土壤中的分类群,并与先前研究中记录的分类群相匹配。该阵列还鉴定出了与Leptodontium、Cadophora、Zalerion和Geomyces有亲缘关系的近缘分类群。通过克隆和DNA测序进一步证实了这些分类群的存在。少数谱系具有低熔点的DNA靶标,除非在损害特异性的条件下,否则在阵列上无法检测到。基于膜的ITS宏阵列与群落ITS探针相结合,具有足够的能力在复杂样品中检测多属水平的真菌谱系,在真菌群落研究中具有广泛的应用前景。
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Hybridization of an ITS-based macroarray with ITS community probes for characterization of complex communities of fungi and fungal-like protists

The ability to characterize fungal community structure and dynamics in the environment is constantly challenged by the high levels of diversity that must be confronted. Large-scale oligonucleotide arrays for use in such analytical studies are currently under development; however, the implementation of this approach generally requires substantial time and financial resources. To address the need for a more accessible tool for fungal community profiling and broad diagnostics, we evaluated the potential utility of a reverse dot blot approach utilizing macroarray targets and probes that each consisted of a PCR product of the entire fungal ITS1–5.8S–ITS2 gene region. Samples used to generate the array targets included both culturable and non-culturable fungi and fungal-like protists representing a range of ecological functions. Tests performed using single-species probes within the genus Pythium demonstrated that taxonomic lineages could generally be distinguished when ITS DNA sequence similarity differed by greater than 5–10 %. An artificially constructed community probe of known composition successfully detected eight of the 10 lineages contained on the array with only one clear false positive in 95 targets. The approach was also successfully applied to environmental samples. Taxa resident in the soil of a local orchard were identified using the array and matched those documented in previous studies. Closely related taxa from a previously uncharacterized and geographically distant orchard soil were also identified by the array and had affinities to Leptodontium, Cadophora, Zalerion, and Geomyces. These taxa were further confirmed to be present in the sample by cloning and DNA sequencing. A minority of lineages had DNA targets with low melting temperatures which were not detected on the arrays except under conditions that compromised specificity. Membrane-based ITS macroarrays coupled with community ITS probes possessed sufficient power to detect multiple genus-level lineages of fungi in complex samples and should have broad applications in the study of fungal communities.

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