Rudi K, Skulberg O M, Skulberg R, Jakobsen K S
Division of General Genetics, Department of Biology, University of Oslo, 0315 Oslo, Norway.
Appl Environ Microbiol. 2000 Sep;66(9):4004-11. doi: 10.1128/AEM.66.9.4004-4011.2000.
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.
从蓝藻培养物中获得的小亚基rRNA基因(16S rDNA)的DNA序列信息,被用于研究自然栖息地中蓝藻的存在情况及其丰度。本研究选取了八个浮游生物群落,它们分别来自藻类生物量相对较低(中营养型)的湖泊以及相应生物量较高(富营养型)的湖泊。利用针对16S rDNA的寡核苷酸探针进行多重序列特异性标记,并将标记后的探针与点样在固体支持物上(DNA阵列)的各自互补序列进行杂交,从而对水样中的生物组成进行基因分析。建立了十个探针,以确定所选湖泊中可识别的蓝藻的相对丰度。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。在随后对自然蓝藻群落的分析中,为所研究的湖泊建立了可重复的丰度图谱。然后将基因分析的结果与通过标准水生生物学和水化学分析获得的信息进行比较。定性地说,在不同湖泊中发现(念珠藻属、微囊藻属和席藻属物种)的生物类群之间存在相对良好的相关性。定量数据的相关性水平较低。然而,这可能是由于样品处理技术的差异所致。这些比较得出的结论是,基因丰度图谱可为在自然栖息地中分离和定量遗传上不同的蓝藻群体提供基础。