4.6 Article

Was the Last Bacterial Common Ancestor a Monoderm after All?

Journal

GENES
Volume 13, Issue 2, Pages -

Publisher

MDPI
DOI: 10.3390/genes13020376

Keywords

bacterial evolution; cell-wall; outer membrane (OM); Bayesian inference (BI); phylogenomics; comparative genomics; ancestral traits

Funding

  1. Belgian Program on Interuniversity Poles of Attraction [P6/19]
  2. Walloon Region [1117545]
  3. University of Liege Credit de demarrage 2012 [SFRD-12/04]
  4. F.R.S.-FNRS Credit de recherche 2014 [CDR J.0080.15]
  5. FRIA (Fonds de la Recherche pour l'Industrie et l'Agriculture) fellowships (F.R.S.-FNRS, Brussels, Belgium)

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The nature of the last bacterial common ancestor and the characteristics of its cell wall are critical for understanding the evolution of life on Earth. Recent research suggests that all known bacteria may have evolved from a common ancestor with a monoderm cell wall structure, challenging the idea that the appearance of the outer membrane was a unique event.
The very nature of the last bacterial common ancestor (LBCA), in particular the characteristics of its cell wall, is a critical issue to understand the evolution of life on earth. Although knowledge of the relationships between bacterial phyla has made progress with the advent of phylogenomics, many questions remain, including on the appearance or disappearance of the outer membrane of diderm bacteria (also called Gram-negative bacteria). The phylogenetic transition between monoderm (Gram-positive bacteria) and diderm bacteria, and the associated peptidoglycan expansion or reduction, requires clarification. Herein, using a phylogenomic tree of cultivated and characterized bacteria as an evolutionary framework and a literature review of their cell-wall characteristics, we used Bayesian ancestral state reconstruction to infer the cell-wall architecture of the LBCA. With the same phylogenomic tree, we further revisited the evolution of the division and cell-wall synthesis (dcw) gene cluster using homology- and model-based methods. Finally, extensive similarity searches were carried out to determine the phylogenetic distribution of the genes involved with the biosynthesis of the outer membrane in diderm bacteria. Quite unexpectedly, our analyses suggest that all cultivated and characterized bacteria might have evolved from a common ancestor with a monoderm cell-wall architecture. If true, this would indicate that the appearance of the outer membrane was not a unique event and that selective forces have led to the repeated adoption of such an architecture. Due to the lack of phenotypic information, our methodology cannot be applied to all extant bacteria. Consequently, our conclusion might change once enough information is made available to allow the use of an even more diverse organism selection.

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