Abstract
Planktonic Archaea have been detected in all the world's oceans and are found from surface waters to the deep sea. The two most common Archaea phyla are Thaumarchaeota and Euryarchaeota. Euryarchaeota are generally more common in surface waters, but very little is known about their ecology and their potential metabolisms. In this study, we explore the genomic ecology of the Marine Group II (MGII), the main marine planktonic Euryarchaeota, and test if it is composed of different ecologically relevant units. We re‐analyzed Tara Oceans metagenomes from the photic layer and the deep ocean by annotating sequences against a custom MGII database and by mapping gene co‐occurrences. Our data provide a global view of the distribution of Euryarchaeota, and more specifically of MGII subgroups, and reveal their association to a number of gene‐coding sequences. In particular, we show that MGII proteorhodopsins were detected in both the surface and the deep chlorophyll maximum layer and that different clusters of these light harvesting proteins were present. Our approach helped describing the set of genes found together with specific MGII subgroups. We could thus define genomic environments that could theoretically describe ecologically meaningful units and the ecological niche that they occupy.
Highlights
The pioneering works published Fuhrman, McCallum, and Davis (1992) and DeLong (1992) revealed the presence of aerobic and me‐ sophilic archaea in both costal surface waters and in the deep ocean
A recent study based on metagenome‐assembled genomes (MAGs) proposes Marine Group II (MGII) as an order‐level lineage that would be named Candidatus Poseidoniales (Rinke et al, 2018)
We focused on 135 Tara Oceans metagenomes corresponding to 63 stations that comprised 63 samples from the surface ocean (SRF), 42 from the deep chlorophyll maximum (DCM), and 30 from the mesopelagic zone (MES) (Table S1)
Summary
The pioneering works published Fuhrman, McCallum, and Davis (1992) and DeLong (1992) revealed the presence of aerobic and me‐ sophilic archaea in both costal surface waters and in the deep ocean. A MGIIa genome was assembled from surface ocean metagenomes (Iverson et al, 2012) and genomic fragments from a MGIIb with a low GC content was recently reconstructed from deep chlorophyll maximum samples and proposed as represen‐ tative for a new class called Thalassoarchaea (Martin‐Cuadrado et al, 2015). These observations draw the picture of a complex ecological structure within the MGIIa and MGIIb, and the question remains as whether the phylogenetic diversity observed within the clades cor‐ responds to the presence of different ecologically relevant taxa. We calculated patterns of co‐occurrences between 16S rRNA and functional genes to infer the genomic environment of MGII subgroups
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