Comprehensive phylogenomics of Methylobacterium reveals four evolutionary distinct groups and underappreciated phyllosphere diversity.
Jean‐Baptiste LeducqiD, David SneddoniD, Malia A SantosiD, Domitille Condrain-Morel, Geneviève Bourret, Norma Cecilia Martinez-GomeziD, Jessica A. LeeiD, James A. FosteriD, Sergey M. StolyariD, B. Jesse ShapiroiD, Steven W. KembeliD, Jack M. SullivaniD, Christopher J. MarxiD
Abstract
Methylobacterium is a group of methylotrophic microbes associated with soil, fresh water, and particularly the phyllosphere, the aerial part of plants that has been well-studied in terms of physiology but whose evolutionary history and taxonomy are unclear. Recent work has suggested that Methylobacterium is much more diverse than thought previously, questioning its status as an ecologically and phylogenetically coherent taxonomic genus. However, taxonomic and evolutionary studies of Methylobacterium have mostly been restricted to model species, often isolated from habitats other than the phyllosphere, and have yet to utilize comprehensive phylogenomic methods to examine gene trees, gene content, or synteny. By analyzing 189 Methylobacterium genomes from a wide range of habitats, including the phyllosphere, we inferred a robust phylogenetic tree while explicitly accounting for the impact of horizontal gene transfers. We showed that Methylobacterium contains four evolutionary distinct groups of bacteria (namely A, B, C, D), characterized by different genome size, GC content, gene content and genome architecture, revealing the dynamic nature of Methylobacterium genomes. In addition of recovering 59 described species, we identified 45 candidate species, mostly phyllosphere-associated, stressing the significance of plants as a reservoir of Methylobacterium diversity. We inferred an ancient transition from a free-living lifestyle to association with plant roots in Methylobacteriaceae ancestor, followed by phyllosphere association of three of the major groups (A, B, D), which early branching in Methylobacterium history was heavily obscured by HGT. Together, our work lays the foundations for a thorough redefinition of Methylobacterium taxonomy, beginning with the abandon of Methylorubrum.
02 /Specification & Classification
Click any tag to browse matching papers- Citations
- 35
- FWCI
- 2.37
- Field percentile
- top 9%
- Organism
- Assay
- Research Focus
- Approach
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Metapangenomics reveals host-driven adaptations of Methylobacterium to the phyllosphere
Jocelyn Lauzon, Jean‐Baptiste Leducq, Steven W. Kembel·bioRxiv·Jul 30, 2026
- A phylogenomic and metagenomic meta-analysis of bacterial diversity in the phyllosphere lifts a veil on Hyphomicrobiales dark matter
Jean‐Baptiste Leducq, Louis-Philippe St-Amand, … Steven W. Kembel·Systematic and Applied MicrobiologyPeer-reviewed·Feb 10, 2026
- Life on leaves left a lasting mark on the Methylobacterium core genome
Jean-Baptiste Leducq, David Sneddon, … Christopher J Marx·bioRxiv·Nov 4, 2026
- Fine-scale adaptations to environmental variation and growth strategies drive phyllosphere Methylobacterium diversity.
J.-B. Leducq, E. Seyer-Lamontagne, … S. W. Kembel·bioRxiv·Jun 4, 2021
- Uncovering hidden phylo- and ecogenomic diversity of the widespread methanotrophic genus Methylobacter
Magdalena Wutkowska, Justus Amuche Nweze, … Anne Daebeler·FEMS Microbiology EcologyPeer-reviewed·Dec 12, 2025
- Richness and composition of phyllosphere Methylobacterium communities cause variation in Arabidopsis thaliana growth
Jocelyn Lauzon, Jérémie Pelletier, … Steven W. Kembel·bioRxiv·Aug 30, 2024