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Application of Sequence-Specific Labeled 16S rRNA Gene Oligonucleotide Probes for Genetic Profiling of Cyanobacterial Abundance and Diversity by Array Hybridization

机译:序列特异性标记的16S rRNA基因寡核苷酸探针在阵列杂交蓝藻丰度和多样性遗传分析中的应用

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摘要

DNA sequence information for the small-subunit rRNA gene (16S rDNA) obtained from cyanobacterial cultures was used to investigate the presence of cyanobacteria and their abundance in natural habitats. Eight planktonic communities developing in lakes characterized by relatively low algal biomass (mesotrophic) and in lakes with correspondingly high biomass (eutrophic) were selected for the study. The organismal compositions of the water samples were analyzed genetically, using multiplex sequence-specific labeling of oligonucleotide probes targeted to 16S rDNA and subsequent hybridization of the labeled probes to their respective complements spotted onto a solid support (DNA array). Ten probes were established to determine the relative abundances of the discernible cyanobacteria encountered in the selected lakes. The probes were generally specific for their targets, as determined through analyses of clone cultures. Reproducible abundance profiles were established for the lakes investigated in the subsequent analyses of natural cyanobacterial communities. The results from the genetic analyses were then compared with information obtained from standard hydrobiological and hydrochemical analyses. Qualitatively, there were relatively good correlations among the groups of organisms (Nostoc, Microcystis, and Planktothrix species) found in the different lakes. The levels of correlation were lower for the quantitative data. This may, however, be due to differences in sample processing technique. The conclusions from these comparisons are that the genetic abundance profiles may provide a foundation for separating and quantifying genetically distinct groups of cyanobacteria in their natural habitats.
机译:从蓝细菌培养物中获得的小亚基rRNA基因(16S rDNA)的DNA序列信息用于研究蓝细菌的存在及其在自然栖息地中的丰度。选择在藻类生物量相对较低的湖泊(中营养)和生物量相对较高的湖泊(富营养化)的八个浮游生物群落中进行研究。使用多重序列特异性标记的寡核苷酸探针靶向16S rDNA,然后将标记的探针与固相支持物(DNA阵列)上的各自互补序列杂交,对水样的生物成分进行了遗传分析。建立了十个探针以确定在选定的湖泊中遇到的可辨别的蓝细菌的相对丰度。通过对克隆培养物的分析确定,这些探针通常对其靶标具有特异性。在随后的天然蓝细菌群落分析中,为所调查的湖泊建立了可再现的丰度分布图。然后将遗传分析的结果与标准水生生物学和水化学分析获得的信息进行比较。定性地,在不同湖泊中发现的生物群(Nostoc,Microcystis和Planktothrix物种)之间具有相对良好的相关性。定量数据的相关程度较低。但是,这可能是由于样品处理技术的差异所致。从这些比较得出的结论是,遗传丰度图谱可为分离和量化其自然栖息地中蓝细菌的遗传不同群体提供基础。

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