Convergent evolution of intestinal lineages in the phylum Methanobacteriota

BACKGROUND: Representatives of the phylum Methanobacteriota occur in various anoxic environments, but only members of the genera Methanosphaera and Methanobrevibacter exclusively colonize the digestive tract of animals. Recent phylogenomic analyses revealed that the genus Methanobrevibacter, which harbors the majority of the intestinal species, is severely underclassified and represents a family-level taxon, "Methanobrevibacteraceae", that evolved entirely in the digestive tract of animals. RESULTS: produced by the hydrogenosomes of their anaerobic hosts. CONCLUSIONS: Our results reveal that the transition of free-living Methanobacteriota to a host-associated lifestyle involves the same genomic changes that were previously recognized in gut bacteria and bacterial endosymbionts of protists, reflecting resemblances between the two prokaryotic domains that are caused by evolutionary convergence in similar environments.

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Publication Details

Journal
Microbiome
Published
2026-05-02
DOI
https://doi.org/10.1186/s40168-026-02434-5
Primary Topic
Anaerobic Digestion and Biogas Production
Type
article
Field-Weighted Citation Impact
0.00

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article

Convergent evolution of intestinal lineages in the phylum Methanobacteriota

Sebastian Cristian Treitli, Undine S. Mies, E. A. Protasov, Andreas Brune et al.
Microbiome
Anaerobic Digestion and Biogas Production
article

Convergent evolution of intestinal lineages in the phylum Methanobacteriota

Sebastian Cristian Treitli, Undine S. Mies, E. A. Protasov, Andreas Brune, Katja Platt, Cathrin Spröer, Boyke Bunk
article en

Abstract

BACKGROUND: Representatives of the phylum Methanobacteriota occur in various anoxic environments, but only members of the genera Methanosphaera and Methanobrevibacter exclusively colonize the digestive tract of animals. Recent phylogenomic analyses revealed that the genus Methanobrevibacter, which harbors the majority of the intestinal species, is severely underclassified and represents a family-level taxon, "Methanobrevibacteraceae", that evolved entirely in the digestive tract of animals. RESULTS: produced by the hydrogenosomes of their anaerobic hosts. CONCLUSIONS: Our results reveal that the transition of free-living Methanobacteriota to a host-associated lifestyle involves the same genomic changes that were previously recognized in gut bacteria and bacterial endosymbionts of protists, reflecting resemblances between the two prokaryotic domains that are caused by evolutionary convergence in similar environments.

MicrobiomeVol. 14(1)
Max Planck Institute for Terrestrial Microbiology (DE), Leibniz Institute DSMZ – German Collection of Microorganisms and Cell Cultures (DE)
Max-Planck-Institut für Terrestrische Mikrobiologie
Openalex Percentile: Top 13%
Anaerobic Digestion and Biogas Production
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