Pierella Karlusich Juan José, Pelletier Eric, Zinger Lucie, Lombard Fabien, Zingone Adriana, Colin Sébastien, Gasol Josep M, Dorrell Richard G, Henry Nicolas, Scalco Eleonora, Acinas Silvia G, Wincker Patrick, de Vargas Colomban, Bowler Chris
Institut de Biologie de l'ENS (IBENS), Département de Biologie, École normale supérieure, CNRS, INSERM, Université PSL, Paris, France.
CNRS Research Federation for the study of Global Ocean Systems Ecology and Evolution, FR2022/Tara Oceans GOSEE, Paris, France.
Mol Ecol Resour. 2023 Jan;23(1):16-40. doi: 10.1111/1755-0998.13592. Epub 2022 Feb 16.
Phytoplankton account for >45% of global primary production, and have an enormous impact on aquatic food webs and on the entire Earth System. Their members are found among prokaryotes (cyanobacteria) and multiple eukaryotic lineages containing chloroplasts. Genetic surveys of phytoplankton communities generally consist of PCR amplification of bacterial (16S), nuclear (18S) and/or chloroplastic (16S) rRNA marker genes from DNA extracted from environmental samples. However, our appreciation of phytoplankton abundance or biomass is limited by PCR-amplification biases, rRNA gene copy number variations across taxa, and the fact that rRNA genes do not provide insights into metabolic traits such as photosynthesis. Here, we targeted the photosynthetic gene psbO from metagenomes to circumvent these limitations: the method is PCR-free, and the gene is universally and exclusively present in photosynthetic prokaryotes and eukaryotes, mainly in one copy per genome. We applied and validated this new strategy with the size-fractionated marine samples collected by Tara Oceans, and showed improved correlations with flow cytometry and microscopy than when based on rRNA genes. Furthermore, we revealed unexpected features of the ecology of these ecosystems, such as the high abundance of picocyanobacterial aggregates and symbionts in the ocean, and the decrease in relative abundance of phototrophs towards the larger size classes of marine dinoflagellates. To facilitate the incorporation of psbO in molecular-based surveys, we compiled a curated database of >18,000 unique sequences. Overall, psbO appears to be a promising new gene marker for molecular-based evaluations of entire phytoplankton communities.
浮游植物占全球初级生产的45%以上,对水生食物网和整个地球系统有着巨大影响。其成员包括原核生物(蓝细菌)以及多个含有叶绿体的真核生物谱系。浮游植物群落的基因调查通常包括从环境样本中提取的DNA对细菌(16S)、核(18S)和/或叶绿体(16S)rRNA标记基因进行PCR扩增。然而,我们对浮游植物丰度或生物量的认识受到PCR扩增偏差、不同分类群rRNA基因拷贝数变异以及rRNA基因无法提供光合作用等代谢特征信息的限制。在此,我们针对宏基因组中的光合基因psbO来规避这些限制:该方法无需PCR,且该基因普遍且仅存在于光合原核生物和真核生物中,每个基因组主要有一个拷贝。我们用塔拉海洋项目收集的大小分级海洋样本应用并验证了这一新策略,结果表明与基于rRNA基因的方法相比,该策略与流式细胞术和显微镜观察的相关性更好。此外,我们揭示了这些生态系统生态学的一些意外特征,例如海洋中微微型蓝细菌聚集体和共生体丰度很高,以及光合生物在较大尺寸的海洋甲藻中的相对丰度下降。为便于在基于分子的调查中纳入psbO,我们编制了一个包含超过18000个独特序列的精选数据库。总体而言,psbO似乎是用于基于分子的整个浮游植物群落评估的一个很有前景的新基因标记。