Nicolas Parisot, Simonetta Gribaldo, Guillaume Borrel, Pierre Peyret, Kasie Raymann, Eric Peyretaillade, Nadia Gaci, William Tottey, Jean-François Brugère, Hugh M. B. Harris, Olivier Bardot, Paul W. O'Toole, Conception, Ingénierie et Développement de l'Aliment et du Médicament (CIDAM), Université d'Auvergne - Clermont-Ferrand I (UdA), School of Microbiology and Alimentary Pharmabiotic Centre, University College Cork (UCC), Laboratoire Microorganismes : Génome et Environnement (LMGE), Université Blaise Pascal - Clermont-Ferrand 2 (UBP)-Université d'Auvergne - Clermont-Ferrand I (UdA)-Centre National de la Recherche Scientifique (CNRS), Génétique, Reproduction et Développement (GReD), Institut National de la Santé et de la Recherche Médicale (INSERM)-Université Clermont Auvergne [2017-2020] (UCA [2017-2020])-Centre National de la Recherche Scientifique (CNRS), Biologie Moléculaire du Gène chez les Extrêmophiles (BMGE), Institut Pasteur [Paris] (IP), Cellule Pasteur UPMC, Université Pierre et Marie Curie - Paris 6 (UPMC)-Institut Pasteur [Paris] (IP), This work was supported by three PhD. Scholarship supports, one from the 'Direction Générale de l'Armement' (DGA) to N.P., one from the French 'Ministère de l'Enseignement Supérieur et de la Recherche' to N.G. and one of the European Union (UE) and the Auvergne Council to W.T. (FEDER). P.W.O.T. was supported by Science Foundation Ireland through a Principal Investigator award, by a CSET award to the Alimentary Pharmabiotic Centre, and by an FHRI award to the ELDERMET project by the Dept. Agriculture, Fisheries and Marine of the Government of Ireland. SG is supported by the Investissement d'Avenir grant 'Ancestrome' (ANR-10- BINF-01-01). KR is a scholar from the Pasteur - Paris University (PPU) International PhD program and receives a stipend from the Paul W. Zuccaire Foundation. JFB thanks the 'centre hospitalier Paul Ardier' in Issoire, especially Dr Mansoor, Dr Denozi and their staff for their valuable help, and Agnès Mihajlovski for her help in initiating this project., ANR-10-BINF-0001,ANCESTROME,Approche de phylogénie intégrative pour la reconstruction de génomes ancestraux(2010), Université Blaise Pascal - Clermont-Ferrand 2 (UBP)-Centre National de la Recherche Scientifique (CNRS)-Université d'Auvergne - Clermont-Ferrand I (UdA), Centre National de la Recherche Scientifique (CNRS)-Université Clermont Auvergne [2017-2020] (UCA [2017-2020])-Institut National de la Santé et de la Recherche Médicale (INSERM), Institut Pasteur [Paris], Institut Pasteur [Paris]-Université Pierre et Marie Curie - Paris 6 (UPMC), BMC, Ed., and Bio-informatique - Approche de phylogénie intégrative pour la reconstruction de génomes ancestraux - - ANCESTROME2010 - ANR-10-BINF-0001 - BINF - VALID
Background A seventh order of methanogens, the Methanomassiliicoccales, has been identified in diverse anaerobic environments including the gastrointestinal tracts (GIT) of humans and other animals and may contribute significantly to methane emission and global warming. Methanomassiliicoccales are phylogenetically distant from all other orders of methanogens and belong to a large evolutionary branch composed by lineages of non-methanogenic archaea such as Thermoplasmatales, the Deep Hydrothermal Vent Euryarchaeota-2 (DHVE-2, Aciduliprofundum boonei) and the Marine Group-II (MG-II). To better understand this new order and its relationship to other archaea, we manually curated and extensively compared the genome sequences of three Methanomassiliicoccales representatives derived from human GIT microbiota, “Candidatus Methanomethylophilus alvus", “Candidatus Methanomassiliicoccus intestinalis” and Methanomassiliicoccus luminyensis. Results Comparative analyses revealed atypical features, such as the scattering of the ribosomal RNA genes in the genome and the absence of eukaryotic-like histone gene otherwise present in most of Euryarchaeota genomes. Previously identified in Thermoplasmatales genomes, these features are presently extended to several completely sequenced genomes of this large evolutionary branch, including MG-II and DHVE2. The three Methanomassiliicoccales genomes share a unique composition of genes involved in energy conservation suggesting an original combination of two main energy conservation processes previously described in other methanogens. They also display substantial differences with each other, such as their codon usage, the nature and origin of their CRISPRs systems and the genes possibly involved in particular environmental adaptations. The genome of M. luminyensis encodes several features to thrive in soil and sediment conditions suggesting its larger environmental distribution than GIT. Conversely, “Ca. M. alvus” and “Ca. M. intestinalis” do not present these features and could be more restricted and specialized on GIT. Prediction of the amber codon usage, either as a termination signal of translation or coding for pyrrolysine revealed contrasted patterns among the three genomes and suggests a different handling of the Pyl-encoding capacity. Conclusions This study represents the first insights into the genomic organization and metabolic traits of the seventh order of methanogens. It suggests contrasted evolutionary history among the three analyzed Methanomassiliicoccales representatives and provides information on conserved characteristics among the overall methanogens and among Thermoplasmata. Electronic supplementary material The online version of this article (doi:10.1186/1471-2164-15-679) contains supplementary material, which is available to authorized users.