Microbial community assembly and evolution in subseafloor sediment

Bacterial and archaeal communities inhabiting the subsurface seabed live under strong energy limitation and have growth rates that are orders of magnitude slower than laboratory-grown cultures. It is not understood how subsurface microbial communities are assembled and whether populations undergo ad...

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Detalhes bibliográficos
Principais autores: Starnawski, Piotr, Bataillon, Thomas, Ettema, Thijs J. G., Jochum, Lara M., Schreiber, Lars, Chen, Xihan, Lever, Mark A., Jørgensen, Bo B., Kjeldsen, Kasper U., Polz, Martin F, Schramm, Andreas
Outros Autores: Massachusetts Institute of Technology. Department of Civil and Environmental Engineering
Formato: Artigo
Publicado em: National Academy of Sciences (U.S.) 2017
Acesso em linha:http://hdl.handle.net/1721.1/112220
https://orcid.org/0000-0001-9296-3733
Descrição
Resumo:Bacterial and archaeal communities inhabiting the subsurface seabed live under strong energy limitation and have growth rates that are orders of magnitude slower than laboratory-grown cultures. It is not understood how subsurface microbial communities are assembled and whether populations undergo adaptive evolution or accumulate mutations as a result of impaired DNA repair under such energy-limited conditions. Here we use amplicon sequencing to explore changes of microbial communities during burial and isolation from the surface to the > 5,000-y-old subsurface of marine sediment and identify a small core set of mostly uncultured bacteria and archaea that is present throughout the sediment column. These persisting populations constitute a small fraction of the entire community at the surface but become predominant in the subsurface. We followed patterns of genome diversity with depth in four dominant lineages of the persisting populations by mapping metagenomic sequence reads onto single-cell genomes. Nucleotide sequence diversity was uniformly low and did not change with age and depth of the sediment. Likewise, therewas no detectable change inmutation rates and efficacy of selection. Our results indicate that subsurface microbial communities predominantly assemble by selective survival of taxa able to persist under extreme energy limitation.