12
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      In marine Bacteroidetes the bulk of glycan degradation during algae blooms is mediated by few clades using a restricted set of genes

      research-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          We investigated Bacteroidetes during spring algae blooms in the southern North Sea in 2010–2012 using a time series of 38 deeply sequenced metagenomes. Initial partitioning yielded 6455 bins, from which we extracted 3101 metagenome-assembled genomes (MAGs) including 1286 Bacteroidetes MAGs covering ~120 mostly uncultivated species. We identified 13 dominant, recurrent Bacteroidetes clades carrying a restricted set of conserved polysaccharide utilization loci (PULs) that likely mediate the bulk of bacteroidetal algal polysaccharide degradation. The majority of PULs were predicted to target the diatom storage polysaccharide laminarin, alpha-glucans, alpha-mannose-rich substrates, and sulfated xylans. Metaproteomics at 14 selected points in time revealed expression of SusC-like proteins from PULs targeting all of these substrates. Analyses of abundant key players and their PUL repertoires over time furthermore suggested that fewer and simpler polysaccharides dominated early bloom stages, and that more complex polysaccharides became available as blooms progressed.

          Related collections

          Most cited references46

          • Record: found
          • Abstract: not found
          • Article: not found

          Primary Production of the Biosphere: Integrating Terrestrial and Oceanic Components

          C Field (1998)
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            The evolution of cooperation within the gut microbiota

            Cooperative phenotypes are considered central to the functioning of microbial communities in many contexts, including communication via quorum sensing, biofilm formation, antibiotic resistance, and pathogenesis 1-5 . The human intestine houses a dense and diverse microbial community critical to health 1,2,4-9 , yet we know little about cooperation within this important ecosystem. Here we experimentally test for evolved cooperation within the Bacteroidales, the dominant Gram-negative bacteria of the human intestine. We show that during growth on certain dietary polysaccharides, the model member Bacteroides thetaiotaomicron exhibits only limited cooperation. Although this organism digests these polysaccharides extracellularly, mutants lacking this ability are outcompeted. In contrast, we discovered a dedicated cross-feeding enzyme system in the prominent gut symbiont Bacteroides ovatus, which digests polysaccharide at a cost to itself but at a benefit to another species. Using in vitro systems and gnotobiotic mouse colonization models, we find that extracellular digestion of inulin increases the fitness of B.ovatus due to reciprocal benefits when it feeds other gut species such as Bacteroides vulgatus. This is a rare example of naturally-evolved cooperation between microbial species. Our study reveals both the complexity and importance of cooperative phenotypes within the mammalian intestinal microbiota.
              Bookmark
              • Record: found
              • Abstract: not found
              • Article: not found

              The ecology of Cytophaga-Flavobacteria in aquatic environments.

                Bookmark

                Author and article information

                Contributors
                +49 421 2028 930 , ramann@mpi-bremen.de
                +49 421 2028 976 , hteeling@mpi-bremen.de
                Journal
                ISME J
                ISME J
                The ISME Journal
                Nature Publishing Group UK (London )
                1751-7362
                1751-7370
                17 July 2019
                17 July 2019
                November 2019
                : 13
                : 11
                : 2800-2816
                Affiliations
                [1 ]ISNI 0000 0004 0491 3210, GRID grid.419529.2, Max Planck Institute for Marine Microbiology, ; Celsiusstraße 1, 28359 Bremen, Germany
                [2 ]ISNI 0000 0004 0449 479X, GRID grid.451309.a, DOE Joint Genome Institute, ; 2800 Mitchell Drive, Walnut Creek, CA 94598 USA
                [3 ]GRID grid.5603.0, Institute for Microbiology, University Greifswald, ; Felix-Hausdorff-Straße 8, 17489 Greifswald, Germany
                [4 ]GRID grid.5603.0, Pharmaceutical Biotechnology, Institute of Pharmacy, University Greifswald, ; Felix-Hausdorff-Straße 3, 17487 Greifswald, Germany
                [5 ]GRID grid.482724.f, Institute of Marine Biotechnology, ; Walther-Rathenau-Straße 49a, 17489 Greifswald, Germany
                Author information
                http://orcid.org/0000-0001-7579-8414
                http://orcid.org/0000-0002-9630-5735
                http://orcid.org/0000-0002-7213-3596
                Article
                476
                10.1038/s41396-019-0476-y
                6794258
                31316134
                c05b43c6-9a75-48ff-8229-7ef8ce22ecb3
                © The Author(s) 2019

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 11 April 2019
                : 1 July 2019
                : 4 July 2019
                Funding
                Funded by: FundRef https://doi.org/10.13039/501100001659, Deutsche Forschungsgemeinschaft (German Research Foundation);
                Award ID: TE 813/2-1
                Award ID: BE 3869/4-1
                Award ID: SCHW 595/10-1
                Award ID: AM 73/9-1
                Award Recipient :
                Categories
                Article
                Custom metadata
                © The Author(s), under exclusive licence to International Society for Microbial Ecology 2019

                Microbiology & Virology
                microbial ecology,proteomics,biodiversity,metagenomics
                Microbiology & Virology
                microbial ecology, proteomics, biodiversity, metagenomics

                Comments

                Comment on this article