Institut de Ciències del Mar, CSIC, Barcelona, Spain.
PLoS One. 2009 Sep 29;4(9):e7143. doi: 10.1371/journal.pone.0007143.
Over the last decade, culture-independent surveys of marine picoeukaryotic diversity based on 18S ribosomal DNA clone libraries have unveiled numerous sequences of novel high-rank taxa. This newfound diversity has significantly altered our understanding of marine microbial food webs and the evolution of eukaryotes. However, the current picture of marine eukaryotic biodiversity may be significantly skewed by PCR amplification biases, occurrence of rDNA genes in multiple copies within a single cell, and the capacity of DNA to persist as extracellular material. In this study we performed an analysis of the metagenomic dataset from the Global Ocean Survey (GOS) expedition, seeking eukaryotic ribosomal signatures. This PCR-free approach revealed similar phylogenetic patterns to clone library surveys, suggesting that PCR steps do not impose major biases in the exploration of environmental DNA. The different cell size fractions within the GOS dataset, however, displayed a distinct picture. High protistan diversity in the <0.8 microm size fraction, in particular sequences from radiolarians and ciliates (and their absence in the 0.8-3 microm fraction), suggest that most of the DNA in this fraction comes from extracellular material from larger cells. In addition, we compared the phylogenetic patterns from rDNA and reverse transcribed rRNA 18S clone libraries from the same sample harvested in the Mediterranean Sea. The libraries revealed major differences, with taxa such as pelagophytes or picobiliphytes only detected in the 18S rRNA library. MAST (Marine Stramenopiles) appeared as potentially prominent grazers and we observed a significant decrease in the contribution of alveolate and radiolarian sequences, which overwhelmingly dominated rDNA libraries. The rRNA approach appears to be less affected by taxon-specific rDNA copy number and likely better depicts the biogeochemical significance of marine protists.
在过去的十年中,基于 18S 核糖体 DNA 克隆文库的海洋微型真核生物多样性的非培养调查揭示了许多新的高级分类群的序列。这种新发现的多样性极大地改变了我们对海洋微生物食物网和真核生物进化的理解。然而,目前的海洋真核生物多样性图景可能受到 PCR 扩增偏差、单个细胞内 rDNA 基因的多个拷贝的存在以及 DNA 作为细胞外物质持续存在的能力的显著影响。在这项研究中,我们对全球海洋调查(GOS)考察的宏基因组数据集进行了分析,寻找真核核糖体特征。这种无 PCR 方法揭示了与克隆文库调查相似的系统发育模式,表明 PCR 步骤不会对环境 DNA 的探索产生主要偏差。然而,GOS 数据集中的不同细胞大小分数显示出不同的模式。<0.8 微米大小分数中高度的原生生物多样性,特别是放射虫和纤毛虫的序列(而它们在 0.8-3 微米分数中不存在),表明该分数中的大部分 DNA 来自较大细胞的细胞外物质。此外,我们比较了从同一地中海样本中收获的 rDNA 和逆转录 rRNA 18S 克隆文库的系统发育模式。这些文库显示出重大差异,只有在 18S rRNA 文库中才能检测到 pelagophytes 或 picobiliphytes 等分类群。MAST(海洋鞭毛藻)似乎是潜在的重要捕食者,我们观察到肺泡和放射虫序列的贡献显著减少,它们在 rDNA 文库中占绝对优势。rRNA 方法似乎受分类群特异性 rDNA 拷贝数的影响较小,并且可能更好地描绘了海洋原生生物的生物地球化学意义。