Insights into archaeal evolution and symbiosis from the genomes of a nanoarchaeon and its inferred crenarchaeal host from Obsidian Pool, Yellowstone National Park

Mircea Podar, Kira S. Makarova, David E. Graham, Yuri I. Wolf, Eugene V. Koonin, Anna Louise Reysenbach

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88 Scopus citations

Abstract

Background: A single cultured marine organism, Nanoarchaeum equitans, represents the Nanoarchaeota branch of symbiotic Archaea, with a highly reduced genome and unusual features such as multiple split genes.Results: The first terrestrial hyperthermophilic member of the Nanoarchaeota was collected from Obsidian Pool, a thermal feature in Yellowstone National Park, separated by single cell isolation, and sequenced together with its putative host, a Sulfolobales archaeon. Both the new Nanoarchaeota (Nst1) and N. equitans lack most biosynthetic capabilities, and phylogenetic analysis of ribosomal RNA and protein sequences indicates that the two form a deep-branching archaeal lineage. However, the Nst1 genome is more than 20% larger, and encodes a complete gluconeogenesis pathway as well as the full complement of archaeal flagellum proteins. With a larger genome, a smaller repertoire of split protein encoding genes and no split non-contiguous tRNAs, Nst1 appears to have experienced less severe genome reduction than N. equitans. These findings imply that, rather than representing ancestral characters, the extremely compact genomes and multiple split genes of Nanoarchaeota are derived characters associated with their symbiotic or parasitic lifestyle. The inferred host of Nst1 is potentially autotrophic, with a streamlined genome and simplified central and energetic metabolism as compared to other Sulfolobales.Conclusions: Comparison of the N. equitans and Nst1 genomes suggests that the marine and terrestrial lineages of Nanoarchaeota share a common ancestor that was already a symbiont of another archaeon. The two distinct Nanoarchaeota-host genomic data sets offer novel insights into the evolution of archaeal symbiosis and parasitism, enabling further studies of the cellular and molecular mechanisms of these relationships.Reviewers: This article was reviewed by Patrick Forterre, Bettina Siebers (nominated by Michael Galperin) and Purification Lopez-Garcia.

Original languageEnglish
Article number9
JournalBiology Direct
Volume8
Issue number1
DOIs
StatePublished - Apr 22 2013

Funding

This research was supported by grants from the National Science Foundation (DEB1134877, ALR, MP), from the U.S. Department of Energy, Office of Biological and Environmental Research (DE-SC0006654, MP) and by the Laboratory Directed Research and Development Program of Oak Ridge National Laboratory (ORNL)(MP and DEG). ORNL is managed by UT-Battelle, LLC, for the U.S. Department of Energy under contract DE-AC05-00OR22725. KSM, YF and EVK are supported by the Intramural Research Program of the National Institutes of Health, National Library of Medicine. We thank Steven Allman for flow cytometry cell sorting, members of the MP and ALR labs for technical and bioinformatics support, Kostas Mavrommatis (Joint Genome Institute) for help with kmer frequency analysis, John Spouge (NCBI) for advice on estimation of genome size and Bettina Siebers for suggestions on the metabolic reconstructions. Special thanks go to the Yellowstone National Park Service for coordinating and allowing sampling under permit YELL-2008 -SCI-5714 and to Prof. Karl O. Stetter for advice and his enthusiastic support of Nanoarchaeota research.

FundersFunder number
National Science FoundationDEB1134877
National Institutes of Health
U.S. Department of Energy
Directorate for Biological Sciences1134877
U.S. National Library of MedicineZIALM000073
Biological and Environmental ResearchDE-SC0006654
Oak Ridge National LaboratoryDE-AC05-00OR22725

    Keywords

    • Archaea evolution
    • Hyperthermophiles
    • Single cell genomics
    • Split genes
    • Symbiosis

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