Abstract
Recent genome-resolved metagenomic analyses of microbial communities from diverse environments have led to the discovery of many novel lineages that significantly expand the phylogenetic breadth of Archaea. Here, we report the genomic characterization of a new archaeal family based on five metagenome-assembled genomes retrieved from acid mine drainage sediments. Phylogenomic analyses placed these uncultivated archaea at the root of the candidate phylum Parvarchaeota, which expand this lesser-known phylum into two family levels. Genes involved in environmental adaptation and carbohydrate and protein utilization were identified in the ultra-small genomes (estimated size 0.53–0.76 Mb), indicating a survival strategy in this harsh environment (low pH and high heavy metal content). The detection of genes with homology to sulfocyanin suggested a potential involvement in iron cycling. Nevertheless, the absence of the ability to synthesize amino acids and nucleotides implies that these archaea may acquire these biomolecules from the environment or other community members. Applying evolutionary history analysis to Parvarchaeota suggested that members of the two families could broaden their niches by acquiring the potentials of utilizing different substrates. This study expands our knowledge of the diversity, metabolic capacity, and evolutionary history of the Parvarchaeota.
Highlights
Advances in sequencing technology and computational approaches have enabled the reconstruction of microbial genomes directly from the environment
We proposed that our metagenomicassembled genomes (MAGs) represent a novel family within Parvarchaeota and the name “Candidatus Acidifodinimicrobiaceae” fam. nov., and “Candidatus Acidifodinimicrobium mancum” gen. nov., sp. nov. with the genome serving as the type material deposited in GenBank under accession number GCA_015121965.1
The new Parvarchaeota MAGs recovered from the Acid mine drainage (AMD) sediments have expanded the phylogenetic diversity of this little known archaeal phylum
Summary
Advances in sequencing technology and computational approaches have enabled the reconstruction of microbial genomes directly from the environment. Such efforts have led to the discovery of major new lineages previously missing from the tree of life (Rinke et al, 2013; Baker et al, 2016; Baker et al, 2020). Extreme environments are pervasive landscapes on the planet. Recent genome-resolved metagenomics analyses of these low-diversity environments have retrieved near-complete or even closed genomes for these elusive taxa, resolving their metabolic functions and evolutionary histories and significantly expanding the archaeal phylogenetic tree (Dombrowski et al, 2018; Hug et al, 2016; Rinke et al, 2013; Baker et al, 2020).
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