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      Diversity and ecological footprint of Global Ocean RNA viruses

      1 , 2 , 3 , 1 , 2 , 3 , 1 , 3 , 1 , 2 , 3 , 1 , 3 , 1 , 2 , 1 , 2 , 3 , 1 , 3 , 4 , 1 , 2 , 3 , 5 , 6 , 6 , 7 , 5 , 6 , 5 , 5 , 6 , 5 , 5 , 6 , 5 , 6 , 6 , 8 , 6 , 7 , 6 , 9 , 6 , 8 , 10 , 11 , 12 , 5 , 6 , 13 , 6 , 7 , 1 , 2 , 3 , 4 , 14 , Tara Oceans Coordinators§
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      American Association for the Advancement of Science (AAAS)

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          Abstract

          DNA viruses are increasingly recognized as influencing marine microbes and microbe-mediated biogeochemical cycling. However, little is known about global marine RNA virus diversity, ecology, and ecosystem roles. In this study, we uncover patterns and predictors of marine RNA virus community- and “species”-level diversity and contextualize their ecological impacts from pole to pole. Our analyses revealed four ecological zones, latitudinal and depth diversity patterns, and environmental correlates for RNA viruses. Our findings only partially parallel those of cosampled plankton and show unexpectedly high polar ecological interactions. The influence of RNA viruses on ecosystems appears to be large, as predicted hosts are ecologically important. Moreover, the occurrence of auxiliary metabolic genes indicates that RNA viruses cause reprogramming of diverse host metabolisms, including photosynthesis and carbon cycling, and that RNA virus abundances predict ocean carbon export.

          Patterns and process in RNA viruses

          Viruses are suspected to be lynchpins in ecosystem function, but so far we can only guess at their significance. DNA viruses are increasingly being recognized as significant components of biogeochemical cycling in the oceans. Dominguez-Huerta et al . explored global patterns of marine RNA virus occurrence by extracting virus sequences from Tara Ocean samples. Host prediction analysis identified predominantly protist and fungal hosts plus a few invertebrates. Like double-stranded DNA viruses and their hosts, RNA viruses showed marked depth limitation but little latitudinal change. Auxiliary metabolic genes in the RNA virome indicated that several eukaryote plankton processes are affected by viruses. A group of 11 RNA viruses that significantly influence ocean carbon flux were identified. —CA

          Abstract

          Community- and “species”-level analyses elucidate ecological impacts and roles of marine RNA viruses.

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          VEGAN, a package of R functions for community ecology

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            Primary production of the biosphere: integrating terrestrial and oceanic components

            Integrating conceptually similar models of the growth of marine and terrestrial primary producers yielded an estimated global net primary production (NPP) of 104.9 petagrams of carbon per year, with roughly equal contributions from land and oceans. Approaches based on satellite indices of absorbed solar radiation indicate marked heterogeneity in NPP for both land and oceans, reflecting the influence of physical and ecological processes. The spatial and temporal distributions of ocean NPP are consistent with primary limitation by light, nutrients, and temperature. On land, water limitation imposes additional constraints. On land and ocean, progressive changes in NPP can result in altered carbon storage, although contrasts in mechanisms of carbon storage and rates of organic matter turnover result in a range of relations between carbon storage and changes in NPP.
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              Ocean plankton. Structure and function of the global ocean microbiome.

              Microbes are dominant drivers of biogeochemical processes, yet drawing a global picture of functional diversity, microbial community structure, and their ecological determinants remains a grand challenge. We analyzed 7.2 terabases of metagenomic data from 243 Tara Oceans samples from 68 locations in epipelagic and mesopelagic waters across the globe to generate an ocean microbial reference gene catalog with >40 million nonredundant, mostly novel sequences from viruses, prokaryotes, and picoeukaryotes. Using 139 prokaryote-enriched samples, containing >35,000 species, we show vertical stratification with epipelagic community composition mostly driven by temperature rather than other environmental factors or geography. We identify ocean microbial core functionality and reveal that >73% of its abundance is shared with the human gut microbiome despite the physicochemical differences between these two ecosystems.
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                Author and article information

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                Journal
                Science
                Science
                American Association for the Advancement of Science (AAAS)
                0036-8075
                1095-9203
                June 10 2022
                June 10 2022
                : 376
                : 6598
                : 1202-1208
                Affiliations
                [1 ]Department of Microbiology, The Ohio State University, Columbus, OH 43210, USA.
                [2 ]EMERGE Biology Integration Institute, The Ohio State University, Columbus, OH 43210, USA.
                [3 ]Center of Microbiome Science, The Ohio State University, Columbus, OH 43210, USA.
                [4 ]The Interdisciplinary Biophysics Graduate Program, The Ohio State University, Columbus, Ohio 43210, USA.
                [5 ]Génomique Métabolique, Genoscope, Institut François-Jacob, CEA, CNRS, Univ Evry, Université Paris-Saclay, 91000 Evry, France.
                [6 ]Research Federation for the Study of Global Ocean Systems Ecology and Evolution, FR2022/Tara Oceans GOSEE, 75016 Paris, France.
                [7 ]Nantes Université, École Centrale Nantes, CNRS, LS2N, UMR 6004, F-44000 Nantes, France.
                [8 ]Institut de Biologie de l’Ecole Normale Supérieure, Ecole Normale Supérieure, CNRS, INSERM, Université PSL, 75005 Paris, France.
                [9 ]Sorbonne Université, CNRS, Laboratoire d’Océanographie de Villefanche, LOV, F-06230 Villefranche-sur-mer, France.
                [10 ]Directors’ Research European Molecular Biology Laboratory, 69117 Heidelberg, Germany.
                [11 ]Integrated Research Facility at Fort Detrick, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Fort Detrick, Frederick, MD 21702, USA.
                [12 ]Institute for Chemical Research, Kyoto University, Kyoto 611-0011, Japan.
                [13 ]Département de Biochimie, Microbiologie et Bio-informatique, Université Laval, Québec, QC G1V 0A6, Canada.
                [14 ]Department of Civil, Environmental and Geodetic Engineering, The Ohio State University, Columbus, OH 43210, USA.
                Article
                10.1126/science.abn6358
                35679415
                e0eca6ac-042c-4cb6-8d88-bd468e0b3be5
                © 2022
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