Evidence map›Paper›PMID 38374154›Full record

ArticleMicrobiome2024

Particle-attached bacteria act as gatekeepers in the decomposition of complex phytoplankton polysaccharides.

Feng-Qing Wang, Daniel Bartosik, Chandni Sidhu, Robin Siebers, De-Chen Lu, Anke Trautwein-Schult, Dörte Becher, Bruno Huettel, Johannes Rick, Inga V Kirstein and 6 more

Open access · goldAbstract readVideo-Audio Media
In one paragraph

Article in Microbiome, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
27.5field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

33 citing papers in PubMed, 60 citations in OpenAlex.

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  18. Detergent-based separation of microbes from marine particles.Applied and environmental microbiology · 2025
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

16 authors at 6 institutions in 2 countries.

Feng-Qing WangMax Planck Institute for Marine Microbiology, Celsiusstraße 1, 28359, Bremen, Germany.
Daniel Bartosik *Institute of Pharmacy, University of Greifswald, Felix-Hausdorff-Straße 3, 17489, Greifswald, Germany.
Chandni Sidhu *Max Planck Institute for Marine Microbiology, Celsiusstraße 1, 28359, Bremen, Germany.
Robin SiebersInstitute of Microbiology, University of Greifswald, Felix-Hausdorff-Straße 8, 17489, Greifswald, Germany.
De-Chen LuMax Planck Institute for Marine Microbiology, Celsiusstraße 1, 28359, Bremen, Germany.
Anke Trautwein-SchultInstitute of Microbiology, University of Greifswald, Felix-Hausdorff-Straße 8, 17489, Greifswald, Germany.
Dörte BecherInstitute of Microbiology, University of Greifswald, Felix-Hausdorff-Straße 8, 17489, Greifswald, Germany.
Bruno HuettelMax Planck Genome Centre Cologne, Carl von Linné-Weg 10, 50829, Cologne, Germany.
Johannes RickAlfred Wegener Institute for Polar and Marine Research, Biologische Anstalt Helgoland, Helgoland, 27483, Germany.
Inga V KirsteinAlfred Wegener Institute for Polar and Marine Research, Biologische Anstalt Helgoland, Helgoland, 27483, Germany.
Karen H WiltshireAlfred Wegener Institute for Polar and Marine Research, Biologische Anstalt Helgoland, Helgoland, 27483, Germany.
Thomas SchwederInstitute of Pharmacy, University of Greifswald, Felix-Hausdorff-Straße 3, 17489, Greifswald, Germany.
Bernhard M FuchsMax Planck Institute for Marine Microbiology, Celsiusstraße 1, 28359, Bremen, Germany.
Mia M BengtssonInstitute of Microbiology, University of Greifswald, Felix-Hausdorff-Straße 8, 17489, Greifswald, Germany. mia.bengtsson@uni-greifswald.de.
Hanno TeelingMax Planck Institute for Marine Microbiology, Celsiusstraße 1, 28359, Bremen, Germany. hteeling@mpi-bremen.de.
Rudolf I AmannMax Planck Institute for Marine Microbiology, Celsiusstraße 1, 28359, Bremen, Germany. ramann@mpi-bremen.de.
Max Planck Institute for Marine Microbiology · DEUniversität Greifswald · DEAlfred-Wegener-Institut Helmholtz-Zentrum für Polar- und Meeresforschung · DEInstitute of Marine Biotechnology · DEMax Planck Institute for Plant Breeding Research · DEShandong University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMarine microalgae (phytoplankton) mediate almost half of the worldwide photosynthetic carbon dioxide fixation and therefore play a pivotal role in global carbon cycling, most prominently during massive phytoplankton blooms. Phytoplankton biomass consists of considerable proportions of polysaccharides, substantial parts of which are rapidly remineralized by heterotrophic bacteria. We analyzed the diversity, activity, and functional potential of such polysaccharide-degrading bacteria in different size fractions during a diverse spring phytoplankton bloom at Helgoland Roads (southern North Sea) at high temporal resolution using microscopic, physicochemical, biodiversity, metagenome, and metaproteome analyses.

resultsProminent active 0.2-3 µm free-living clades comprised Aurantivirga, "Formosa", Cd. Prosiliicoccus, NS4, NS5, Amylibacter, Planktomarina, SAR11 Ia, SAR92, and SAR86, whereas BD1-7, Stappiaceae, Nitrincolaceae, Methylophagaceae, Sulfitobacter, NS9, Polaribacter, Lentimonas, CL500-3, Algibacter, and Glaciecola dominated 3-10 µm and > 10 µm particles. Particle-attached bacteria were more diverse and exhibited more dynamic adaptive shifts over time in terms of taxonomic composition and repertoires of encoded polysaccharide-targeting enzymes. In total, 305 species-level metagenome-assembled genomes were obtained, including 152 particle-attached bacteria, 100 of which were novel for the sampling site with 76 representing new species. Compared to free-living bacteria, they featured on average larger metagenome-assembled genomes with higher proportions of polysaccharide utilization loci. The latter were predicted to target a broader spectrum of polysaccharide substrates, ranging from readily soluble, simple structured storage polysaccharides (e.g., laminarin, α-glucans) to less soluble, complex structural, or secreted polysaccharides (e.g., xylans, cellulose, pectins). In particular, the potential to target poorly soluble or complex polysaccharides was more widespread among abundant and active particle-attached bacteria.

conclusionsParticle-attached bacteria represented only 1% of all bloom-associated bacteria, yet our data suggest that many abundant active clades played a pivotal gatekeeping role in the solubilization and subsequent degradation of numerous important classes of algal glycans. The high diversity of polysaccharide niches among the most active particle-attached clades therefore is a determining factor for the proportion of algal polysaccharides that can be rapidly remineralized during generally short-lived phytoplankton bloom events. Video Abstract.

Indexed as

FlavobacteriaceaeMicroalgaeEutrophicationPhytoplanktonPolysaccharidesPolysaccharidesAlgal bloomAlgal polysaccharideBacterioplanktonBacteroidotaCarbohydrate-active enzymeCarbon budgetCarbon cycleFree-living bacteriaHelgoland Roads LTERMarine microbesParticle-attached bacteriaParticulate organic matterPolysaccharide utilization locus

Identifiers

PMID38374154
PMCPMC10877868
OpenAlexW4391969823

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.