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dc.contributor.authorRay, Jessicaeng
dc.contributor.authorDondrup, Michaeleng
dc.contributor.authorModha, Sejaleng
dc.contributor.authorSteen, Ida Heleneeng
dc.contributor.authorSandaa, Ruth-Anneeng
dc.contributor.authorClokie, Marthaeng
dc.date.accessioned2013-04-03T12:15:19Z
dc.date.available2013-04-03T12:15:19Z
dc.date.issued2012-04-11eng
dc.PublishedPLoS ONE 7(4): e34238eng
dc.identifier.issn1932-6203en_US
dc.identifier.urihttps://hdl.handle.net/1956/6475
dc.description.abstractViruses are ubiquitous in the oceans and critical components of marine microbial communities, regulating nutrient transfer to higher trophic levels or to the dissolved organic pool through lysis of host cells. Hydrothermal vent systems are oases of biological activity in the deep oceans, for which knowledge of biodiversity and its impact on global ocean biogeochemical cycling is still in its infancy. In order to gain biological insight into viral communities present in hydrothermal vent systems, we developed a method based on deep-sequencing of pulsed field gel electrophoretic bands representing key viral fractions present in seawater within and surrounding a hydrothermal plume derived from Loki's Castle vent field at the Arctic Mid-Ocean Ridge. The reduction in virus community complexity afforded by this novel approach enabled the near-complete reconstruction of a lambda-like phage genome from the virus fraction of the plume. Phylogenetic examination of distinct gene regions in this lambdoid phage genome unveiled diversity at loci encoding superinfection exclusion- and integrase-like proteins. This suggests the importance of fine-tuning lyosgenic conversion as a viral survival strategy, and provides insights into the nature of host-virus and virus-virus interactions, within hydrothermal plumes. By reducing the complexity of the viral community through targeted sequencing of prominent dsDNA viral fractions, this method has selectively mimicked virus dominance approaching that hitherto achieved only through culturing, thus enabling bioinformatic analysis to locate a lambdoid viral “needle" within the greater viral community “haystack". Such targeted analyses have great potential for accelerating the extraction of biological knowledge from diverse and poorly understood environmental viral communities.en_US
dc.language.isoengeng
dc.publisherPublic Library of Scienceen_US
dc.rightsAttribution CC BYeng
dc.rights.urihttp://creativecommons.org/licenses/by/2.5/eng
dc.titleFinding a Needle in the Virus Metagenome Haystack - Micro-Metagenome Analysis Captures a Snapshot of the Diversity of a Bacteriophage Armoireen_US
dc.typePeer reviewed
dc.typeJournal article
dc.description.versionpublishedVersionen_US
dc.rights.holderCopyright 2012 Ray et al.en_US
dc.identifier.doihttps://doi.org/10.1371/journal.pone.0034238
dc.identifier.cristin959529


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