Evidence map›Paper›PMID 27654921›Full record

ArticleNature2016

Ecogenomics and potential biogeochemical impacts of globally abundant ocean viruses.

Simon Roux, Jennifer R Brum, Bas E Dutilh, Shinichi Sunagawa, Melissa B Duhaime, Alexander Loy, Bonnie T Poulos, Natalie Solonenko, Elena Lara, Julie Poulain and 15 more

Abstract read
PubMed Publisher
In one paragraph

Article in Nature, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 448 papers.

0numbers the graph read from it
0cells of the map it votes in
448citing papers in PubMed
–field-weighted citation impact
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

448 citing papers in PubMed.

  1. Article
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  15. V- and VNature communications · 2026
    Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. Article

388 more citing papers are in PubMed but not listed here.

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

25 authors.

Simon RouxDepartment of Microbiology, The Ohio State University, Columbus, Ohio 43210, USA.
Jennifer R BrumDepartment of Microbiology, The Ohio State University, Columbus, Ohio 43210, USA.
Bas E DutilhTheoretical Biology and Bioinformatics, Utrecht University, 3584 CH Utrecht, The Netherlands.
Shinichi SunagawaStructural and Computational Biology, European Molecular Biology Laboratory, 69117 Heidelberg, Germany.
Melissa B DuhaimeDepartment of Ecology and Evolutionary Biology, University of Michigan, Ann Arbor, Michigan 48109, USA.
Alexander LoyDivision of Microbial Ecology, Department of Microbiology and Ecosystem Science, Research Network Chemistry Meets Microbiology, University of Vienna, A-1090 Vienna, Austria.
Bonnie T PoulosDepartment of Ecology and Evolutionary Biology, University of Arizona, Tucson, Arizona 85721, USA.
Natalie SolonenkoDepartment of Microbiology, The Ohio State University, Columbus, Ohio 43210, USA.
Elena LaraDepartment of Marine Biology and Oceanography, Institut de Ciències del Mar (ICM), CSIC Barcelona E0800, Spain.
Julie PoulainCEA - Institut de Génomique, GENOSCOPE, 91057 Evry, France.
Stéphane PesantPANGAEA, Data Publisher for Earth and Environmental Science, University of Bremen, 28359 Bremen, Germany.
Stefanie Kandels-LewisStructural and Computational Biology, European Molecular Biology Laboratory, 69117 Heidelberg, Germany.
Céline DimierCNRS, UMR 7144, EPEP, Station Biologique de Roscoff, 29680 Roscoff, France.
Marc PicheralCNRS, UMR 7093, Laboratoire d'océanographie de Villefranche, Observatoire Océanologique, 06230 Villefranche-sur-mer, France.
Sarah SearsonCNRS, UMR 7093, Laboratoire d'océanographie de Villefranche, Observatoire Océanologique, 06230 Villefranche-sur-mer, France.
Corinne CruaudCEA - Institut de Génomique, GENOSCOPE, 91057 Evry, France.
Adriana AlbertiCEA - Institut de Génomique, GENOSCOPE, 91057 Evry, France.
Carlos M DuarteMediterranean Institute of Advanced Studies, CSIC-UiB, 21-07190 Esporles, Mallorca, Spain.
Josep M GasolDepartment of Marine Biology and Oceanography, Institut de Ciències del Mar (ICM), CSIC Barcelona E0800, Spain.
Dolors VaquéDepartment of Marine Biology and Oceanography, Institut de Ciències del Mar (ICM), CSIC Barcelona E0800, Spain.
Tara Oceans Coordinators
Peer BorkStructural and Computational Biology, European Molecular Biology Laboratory, 69117 Heidelberg, Germany.
Silvia G AcinasDepartment of Marine Biology and Oceanography, Institut de Ciències del Mar (ICM), CSIC Barcelona E0800, Spain.
Patrick WinckerCEA - Institut de Génomique, GENOSCOPE, 91057 Evry, France.
Matthew B SullivanDepartment of Microbiology, The Ohio State University, Columbus, Ohio 43210, USA.

Funding

Austrian Science Fund FWF P 25111
6 · The paper itself

Abstract

Ocean microbes drive biogeochemical cycling on a global scale. However, this cycling is constrained by viruses that affect community composition, metabolic activity, and evolutionary trajectories. Owing to challenges with the sampling and cultivation of viruses, genome-level viral diversity remains poorly described and grossly understudied, with less than 1% of observed surface-ocean viruses known. Here we assemble complete genomes and large genomic fragments from both surface- and deep-ocean viruses sampled during the Tara Oceans and Malaspina research expeditions, and analyse the resulting 'global ocean virome' dataset to present a global map of abundant, double-stranded DNA viruses complete with genomic and ecological contexts. A total of 15,222 epipelagic and mesopelagic viral populations were identified, comprising 867 viral clusters (defined as approximately genus-level groups). This roughly triples the number of known ocean viral populations and doubles the number of candidate bacterial and archaeal virus genera, providing a near-complete sampling of epipelagic communities at both the population and viral-cluster level. We found that 38 of the 867 viral clusters were locally or globally abundant, together accounting for nearly half of the viral populations in any global ocean virome sample. While two-thirds of these clusters represent newly described viruses lacking any cultivated representative, most could be computationally linked to dominant, ecologically relevant microbial hosts. Moreover, we identified 243 viral-encoded auxiliary metabolic genes, of which only 95 were previously known. Deeper analyses of four of these auxiliary metabolic genes (dsrC, soxYZ, P-II (also known as glnB) and amoC) revealed that abundant viruses may directly manipulate sulfur and nitrogen cycling throughout the epipelagic ocean. This viral catalog and functional analyses provide a necessary foundation for the meaningful integration of viruses into ecosystem models where they act as key players in nutrient cycling and trophic networks.

Indexed as

EcosystemGenome, ViralMetagenomicsDatasets as TopicDNA, ViralEcologyExpeditionsGenes, ViralGeographic MappingMetagenomeNitrogen CycleOceans and SeasSeawaterSulfurVirusesDNA, ViralSulfur

Identifiers

PMID27654921

What OpenQuestion holds

Textmetadata
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 OpenQuestion graph.