Armbrecht Linda, Eisenhofer Raphael, Utge José, Sibert Elizabeth C, Rocha Fabio, Ward Ryan, Pierella Karlusich Juan José, Tirichine Leila, Norris Richard, Summers Mindi, Bowler Chris
Institute for Marine and Antarctic Studies (IMAS), Ecology & Biodiversity Centre, University of Tasmania, Battery Point, TAS, 7004, Australia.
Australian Centre for Ancient DNA, School of Biological Sciences, Faculty of Sciences, The University of Adelaide, Adelaide, SA, 5005, Australia.
ISME Commun. 2021 Nov 9;1(1):66. doi: 10.1038/s43705-021-00070-8.
Sedimentary ancient DNA (sedaDNA) analyses are increasingly used to reconstruct marine ecosystems. The majority of marine sedaDNA studies use a metabarcoding approach (extraction and analysis of specific DNA fragments of a defined length), targeting short taxonomic marker genes. Promising examples are 18S-V9 rRNA (121-130 base pairs, bp) and diat-rbcL (76 bp), targeting eukaryotes and diatoms, respectively. However, it remains unknown how 18S-V9 and diat-rbcL derived compositional profiles compare to metagenomic shotgun data, the preferred method for ancient DNA analyses as amplification biases are minimised. We extracted DNA from five Santa Barbara Basin sediment samples (up to ~11 000 years old) and applied both a metabarcoding (18S-V9 rRNA, diat-rbcL) and a metagenomic shotgun approach to (i) compare eukaryote, especially diatom, composition, and (ii) assess sequence length and database related biases. Eukaryote composition differed considerably between shotgun and metabarcoding data, which was related to differences in read lengths (112 and ~161 bp, respectively), and overamplification of short reads in metabarcoding data. Diatom composition was influenced by reference bias that was exacerbated in metabarcoding data and characterised by increased representation of Chaetoceros, Thalassiosira and Pseudo-nitzschia. Our results are relevant to sedaDNA studies aiming to accurately characterise paleo-ecosystems from either metabarcoding or metagenomic data.
沉积古DNA(sedaDNA)分析越来越多地用于重建海洋生态系统。大多数海洋sedaDNA研究采用元条形码方法(提取和分析特定长度的DNA片段),针对短分类标记基因。有前景的例子是18S-V9 rRNA(约121-130个碱基对,bp)和硅藻rbcL(76 bp),分别针对真核生物和硅藻。然而,18S-V9和硅藻rbcL衍生的组成谱与宏基因组鸟枪法数据相比如何仍不清楚,宏基因组鸟枪法数据是古DNA分析的首选方法,因为扩增偏差最小。我们从五个圣巴巴拉盆地沉积物样本(距今约11000年)中提取了DNA,并应用元条形码(18S-V9 rRNA、硅藻rbcL)和宏基因组鸟枪法方法来(i)比较真核生物,特别是硅藻的组成,以及(ii)评估序列长度和数据库相关偏差。鸟枪法和元条形码数据之间的真核生物组成差异很大,这与读取长度的差异(分别约为112和161 bp)以及元条形码数据中短读取的过度扩增有关。硅藻组成受参考偏差的影响,这种偏差在元条形码数据中加剧,其特征是角毛藻属、海链藻属和拟菱形藻属的代表性增加。我们的结果与旨在从元条形码或宏基因组数据中准确表征古生态系统的sedaDNA研究相关。