Marine Viruses 2016

© 2018 by the authors; CC BY-NC-ND license

evolution; trade-off; cost of resistance; Phycodnavirus; Prasinovirus; environmental change; virus-host interactions; marine viral ecology; Ostreococcus tauri; Emiliania huxleyi; CO₂; ocean acidification; climate change; Coccolithovirus; EhV; Prymnesium parvum; haptophyte; algal bloom; algal virus; Megaviridae; NCLDV; virus–host interactions; marine virus ecology; virus-driven evolution; giant viruses; nucleocytoplasmic large DNA viruses (NCLDVs); Mimiviridae; microbiome; viruses; prokaryote; eukaryote; NGS; diversity; phylotypes; eDNA; meDNA; Piscine orthoreovirus; PRV; non-structural protein; µNS; µ1; expression kinetics; proteolytic cleavage; pathogenesis; blood cells; Atlantic Salmon; Emiliania huxleyi; virus; Phycodnaviridae; EhV; transcriptome; tiling array; E. huxleyi; coccolithovirus; genome comparison; horizontal gene transfer; domains of life; Shewanella; bacteriophage; biofilm; extracellular DNA; Phycodnaviridae; Coccolithovirus; Coccolithophore; Haptophyta; Killing-the-winner; cost of resistance; infectivity trade-offs; algae virus; marine viral ecology; viral-host interactions; Haptophyta; Phycodnaviridae; Megaviridae; viral–host interactions; metagenomics; marine viral ecology; n/a; roseophage; genome; phylogenetic analysis; environmental distribution; bacteriophages; temperate; Vibrio anguillarum; Siphovirus; genetic similarity; omnipresent; lysogenic conversion; Arctic algal viruses; climate change; infectivity; Micromonas virus; prasinovirus; temperature; virus-host interactions; cyanophage; marine Synechococcus; host-virus interactions; host defenses; stress-response genes; gene inactivation; burst-size; PIN-PhoH; viral abundance; environmental variables; multivariate model; Akaike Information Criterion; marine viral diversity; viral–host interaction; high latitude microbes; minimum food web model; copepods; ciliates; nutrient limitation; trophic cascade; n/a