Institute for Limnology, Mondsee, Austria.
Mol Ecol. 2010 Mar;19 Suppl 1(Suppl 1):32-40. doi: 10.1111/j.1365-294X.2009.04478.x.
With the delivery of millions of sequence reads in a single experiment, next-generation sequencing (NGS) is currently revolutionizing surveys of microorganism diversity. In particular, when applied to Eukaryotes, we are still lacking a rigorous comparison of morphological and NGS-based diversity estimates. In this report, we studied the diversity and the seasonal community turnover of alveolates (Ciliophora and Dinophyceae) in an oligotrophic freshwater lake by SSU amplicon sequencing with NGS as well as by classical morphological analysis. We complemented the morphological analysis by single-cell PCR followed by Sanger sequencing to provide an unambiguous link to the NGS data. We show that NGS and morphological analyses generally capture frequency shifts of abundant taxa over our seasonal samples. The observed incongruencies are probably largely due to rDNA copy number variation among taxa and heterogeneity in the efficiency of cell lysis. Overall, NGS-based amplicon sequencing was superior in detecting rare species. We propose that in the absence of other nuclear markers less susceptible to copy number variation, rDNA-based diversity studies need to be adjusted for confounding effects of copy number variation.
随着单实验中数百万个序列读取的交付,下一代测序(NGS)正在彻底改变微生物多样性的调查。特别是,当应用于真核生物时,我们仍然缺乏对形态和基于 NGS 的多样性估计的严格比较。在本报告中,我们通过 NGS 进行了 SSU 扩增子测序以及经典形态分析,研究了贫营养淡水湖中类脂体(纤毛和甲藻)的多样性和季节性群落更替。我们通过单细胞 PCR 补充了形态分析,然后进行 Sanger 测序,为 NGS 数据提供了明确的链接。我们表明,NGS 和形态分析通常可以捕获丰富类群在季节性样本中的频率变化。观察到的不一致可能主要归因于 rDNA 拷贝数变异和细胞裂解效率的异质性。总体而言,基于 NGS 的扩增子测序在检测稀有物种方面具有优势。我们建议,在缺乏其他不易受拷贝数变异影响的核标记的情况下,基于 rDNA 的多样性研究需要针对拷贝数变异的混杂效应进行调整。