Published August 11, 2020 | Version v1
Journal article Open

Microbial strategies for survival in the glass sponge Vazella pourtalesii

  • 1. GEOMAR Helmholtz Centre for Ocean Research Kiel, RD3 Marine Symbioses, Kiel, Germany
  • 2. Department of Fisheries and Oceans, Bedford Institute of Oceanography, Dartmouth, Nova Scotia, Canada
  • 3. Institute for Clinical Molecular Biology, Kiel University, Kiel, Germany
  • 4. Functional Morphology and Biomechanics, Institute of Zoology, Kiel University, Kiel, Germany
  • 5. GEOMAR Helmholtz Centre for Ocean Research Kiel, RD3 Marine Symbioses, Kiel, Germany; Kiel University, Kiel, Germany

Description

ABSTRACT. Few studies have explored the microbiomes of glass sponges (Hexactinellida). The present study seeks to elucidate the composition of the microbiota associated with the glass sponge Vazella pourtalesii and the functional strategies of the main symbionts. We combined microscopic approaches with metagenome-guided microbial genome reconstruction and amplicon community profiling toward this goal. Microscopic imaging revealed that the host and microbial cells appeared within dense biomass patches that are presumably syncytial tissue aggregates. Based on abundances in amplicon libraries and metagenomic data, SAR324 bacteria, Crenarchaeota, Patescibacteria, and Nanoarchaeota were identified as abundant members of the V. pourtalesii microbiome; thus, their genomic potentials were analyzed in detail. A general pattern emerged in that the V. pourtalesii symbionts had very small genome sizes, in the range of 0.5 to 2.2 Mb, and low GC contents, even below those of seawater relatives. Based on functional analyses of metagenome-assembled genomes (MAGs), we propose two major microbial strategies: the “givers", namely, Crenarchaeota and SAR324, heterotrophs and facultative anaerobes, produce and partly secrete all required amino acids and vitamins. The “takers,” Nanoarchaeota and Patescibacteria, are anaerobes with reduced genomes that tap into the microbial community for resources, e.g., lipids and DNA, likely using pilus-like structures. We posit that the existence of microbial cells in sponge syncytia together with the low-oxygen conditions in the seawater environment are factors that shape the unique compositional and functional properties of the microbial community associated with V. pourtalesii.

IMPORTANCE. We investigated the microbial community of V. pourtalesii that forms globally unique, monospecific sponge grounds under low-oxygen conditions on the Scotian Shelf, where it plays a key role in its vulnerable ecosystem. The microbial community was found to be concentrated within biomass patches and is dominated by small cells (<1 μm). MAG analyses showed consistently small genome sizes and low GC contents, which is unusual compared to known sponge symbionts. These properties, as well as the (facultatively) anaerobic metabolism and a high degree of interdependence between the dominant symbionts regarding amino acid and vitamin synthesis, are likely adaptations to the unique conditions within the syncytial tissue of their hexactinellid host and the low-oxygen environment.

Notes

ACKNOWLEDGEMENTS. The project "SponGES" received funding from the European Union's Horizon 2020 research and innovation program under grant agreement no. 679849. We thank our colleague Hans Tore Rapp for leading this great consortium for the last 4 years; you are dearly missed. Ship time and Canadian participation were enabled by Fisheries and Oceans Canada's (DFO) International Governance Strategy Science Program through project "Marine Biological Diversity Beyond Areas of National Jurisdiction (BBNJ): 3-Tiers of Diversity (Genes-Species-Communities)," led by E.K. (2017 to 2019). We acknowledge financial support by Land Schleswig-Holstein within the funding programme Open Access Publikations-fonds. We appreciated the onboard support of the crew and scientific party of the expedition MLB2017001. Fred Whoriskey provided the OTN mooring samples. Andrea Hethke, Ina Clefsen, and the CRC1182 Z3 team (Katja Cloppenborg-Schmidt, Malte Rühlemann, and John Baines) provided valuable support with the amplicon pipeline. Further, we thank the following people for microscopy-related support: Yu-Chen Wu, Marie Sieberns, Anke Bleyer, Cay Kruse, and Julia-Vanessa Böge. Martin Jahn provided advice for metabolic analyses. DATA DEPOSITION. Detailed sample metadata was deposited in the PANGAEA database (https://doi .pangaea.de/10.1594/PANGAEA.917599). Amplicon and metagenomic raw read data were deposited in the NCBI database under BioProject PRJNA613976. Individual accession numbers for assembled MAGs are listed in Table S1. Interpro annotation output is available on figshare at https://doi.org/10.6084/m9 .figshare.12280313. Copyright © 2020 Bayer et al.

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Funding

SponGES – Deep-sea Sponge Grounds Ecosystems of the North Atlantic: an integrated approach towards their preservation and sustainable exploitation 679849
European Commission