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本文引用的文献

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The role of ciliated protozoa in pelagic freshwater ecosystems.纤毛原生动物在远洋淡水生态系统中的作用。
Microb Ecol. 1989 Mar;17(2):111-36. doi: 10.1007/BF02011847.
2
Bacterivory and herbivory: Key roles of phagotrophic protists in pelagic food webs.噬菌作用和食草作用:浮游生物食物网中吞噬性原生动物的关键作用。
Microb Ecol. 1994 Sep;28(2):223-35. doi: 10.1007/BF00166812.
3
Multiple alignment of DNA sequences with MAFFT.使用MAFFT对DNA序列进行多重比对。
Methods Mol Biol. 2009;537:39-64. doi: 10.1007/978-1-59745-251-9_3.
4
Environmental rRNA inventories miss over half of protistan diversity.环境rRNA清单遗漏了超过一半的原生生物多样性。
BMC Microbiol. 2008 Dec 16;8:222. doi: 10.1186/1471-2180-8-222.
5
Protists are microbes too: a perspective.原生生物也是微生物:一种观点。
ISME J. 2009 Jan;3(1):4-12. doi: 10.1038/ismej.2008.101. Epub 2008 Nov 13.
6
Improved methodology for identification of protists and microalgae from plankton samples preserved in Lugol's iodine solution: combining microscopic analysis with single-cell PCR.改进的从保存在卢戈氏碘液中的浮游生物样本中鉴定原生生物和微藻的方法:将显微镜分析与单细胞PCR相结合。
Appl Environ Microbiol. 2008 Apr;74(8):2505-10. doi: 10.1128/AEM.01803-07. Epub 2008 Feb 22.
7
Evidence for geographic isolation and signs of endemism within a protistan morphospecies.原生生物形态物种内地理隔离的证据及特有现象的迹象。
Appl Environ Microbiol. 2006 Aug;72(8):5159-64. doi: 10.1128/AEM.00601-06.
8
Microeukaryote community patterns along an O2/H2S gradient in a supersulfidic anoxic fjord (Framvaren, Norway).超硫化缺氧峡湾(挪威弗拉姆瓦伦)中沿氧气/硫化氢梯度的微型真核生物群落模式。
Appl Environ Microbiol. 2006 May;72(5):3626-36. doi: 10.1128/AEM.72.5.3626-3636.2006.
9
A multiple PCR-primer approach to access the microeukaryotic diversity in environmental samples.一种用于获取环境样本中微型真核生物多样性的多重PCR引物方法。
Protist. 2006 Feb;157(1):31-43. doi: 10.1016/j.protis.2005.10.004. Epub 2006 Jan 23.
10
Mapping of picoeucaryotes in marine ecosystems with quantitative PCR of the 18S rRNA gene.利用18S rRNA基因定量PCR技术对海洋生态系统中的微微型真核生物进行测绘。
FEMS Microbiol Ecol. 2005 Mar 1;52(1):79-92. doi: 10.1016/j.femsec.2004.10.006. Epub 2004 Dec 22.

多样性的隐秘世界:下一代测序技术在真核微生物分子多样性调查中的潜力和局限性。

Diversity in a hidden world: potential and limitation of next-generation sequencing for surveys of molecular diversity of eukaryotic microorganisms.

机构信息

Institute for Limnology, Mondsee, Austria.

出版信息

Mol Ecol. 2010 Mar;19 Suppl 1(Suppl 1):32-40. doi: 10.1111/j.1365-294X.2009.04478.x.

DOI:10.1111/j.1365-294X.2009.04478.x
PMID:20331768
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2953707/
Abstract

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.

摘要

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。