4.5 Article

Marsarchaeota are an aerobic archaeal lineage abundant in geothermal iron oxide microbial mats

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NATURE MICROBIOLOGY
卷 3, 期 6, 页码 732-740

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NATURE PORTFOLIO
DOI: 10.1038/s41564-018-0163-1

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  1. DOE Pacific Northwest National Laboratory [112443, 254840]
  2. DOE Joint Genome Institute Community Sequencing Program [CSP 787081, CSP 701]
  3. National Science Foundation Integrative Graduate Education and Research Traineeship Program [NSF DGE 0654336]
  4. Montana Agricultural Experiment Station
  5. Genomic Science Program, Office of Biological and Environmental Research, US DOE [DOE-AC02-05CH11231]
  6. MSU's Information Technology Center

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The discovery of archaeal lineages is critical to our understanding of the universal tree of life and evolutionary history of the Earth. Geochemically diverse thermal environments in Yellowstone National Park provide unprecedented opportunities for studying archaea in habitats that may represent analogues of early Earth. Here, we report the discovery and characterization of a phylum-level archaeal lineage proposed and herein referred to as the 'Marsarchaeota', after the red planet. The Marsarchaeota contains at least two major subgroups prevalent in acidic, microaerobic geothermal Fe(III) oxide microbial mats across a temperature range from similar to 50-80 degrees C. Metagenomics, single-cell sequencing, enrichment culturing and in situ transcriptional analyses reveal their biogeochemical role as facultative aerobic chemoorganotrophs that may also mediate the reduction of Fe(III). Phylogenomic analyses of replicate assemblies corresponding to two groups of Marsarchaeota indicate that they branch between the Crenarchaeota and all other major archaeal lineages. Transcriptomic analyses of several Fe(III) oxide mat communities reveal that these organisms were actively transcribing two different terminal oxidase complexes in situ and genes comprising an F-420-dependent butanal catabolism. The broad distribution of Marsarchaeota in geothermal, microaerobic Fe(III) oxide mats suggests that similar habitat types probably played an important role in the evolution of archaea.

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