Cell Host & Microbe
Volume 30, Issue 3, 9 March 2022, Pages 314-328.e11
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Article
Diverse events have transferred genes for edible seaweed digestion from marine to human gut bacteria

https://doi.org/10.1016/j.chom.2022.02.001Get rights and content
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Highlights

  • Human gut bacteria have acquired genetic upgrades enabling edible seaweed digestion

  • Bacteroides genes for agarose degradation reside on a large, mobilizable plasmids

  • Some human Firmicutes have also gained the ability to degrade seaweed polysaccharides

  • At least four separate events mobilized porphyran and/or agarose genes into gut bacteria

Summary

Humans harbor numerous species of colonic bacteria that digest fiber polysaccharides in commonly consumed terrestrial plants. More recently in history, regional populations have consumed edible macroalgae seaweeds containing unique polysaccharides. It remains unclear how extensively gut bacteria have adapted to digest these nutrients. Here, we show that the ability of gut bacteria to digest seaweed polysaccharides is more pervasive than previously appreciated. Enrichment-cultured Bacteroides harbor previously discovered genes for seaweed degradation, which have mobilized into several members of this genus. Additionally, other examples of marine bacteria-derived genes, and their mobile DNA elements, are involved in gut microbial degradation of seaweed polysaccharides, including genes in gut-resident Firmicutes. Collectively, these results uncover multiple separate events that have mobilized the genes encoding seaweed-degrading-enzymes into gut bacteria. This work further underscores the metabolic plasticity of the human gut microbiome and global exchange of genes in the context of dietary selective pressures.

Keywords

human gut microbiome
Bacteroides
lateral gene transfer
polysaccharide metabolism

Data and code availability

  • Genome sequence read data for all isolates can be accessed through the National Institutes of Health National Center for Biotechnology Institute (NCBI) database, NCBI Bioproject: PRJNA625151 (Biosample numbers SAMN14593814-45). All RNA-sequencing data can be accessed NCBI Gene Expression Omnibus (GEO) database: GSE149357 (samples GSM4498559-82). Mass spectrometry proteomics data have been deposited to the ProteomeXchange Consortium via the PRIDE (Perez-Riverol et al., 2019) partner repository, ProteomeXchange Consortium: PXD019149.

  • No new code was developed in this study.

  • Any additional information required to reanalyze the data reported in this paper is available from the lead contact upon request.

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11

These authors contributed equally

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Lead contact