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dc.contributor.authorThrash, JC
dc.contributor.authorTemperton, B
dc.contributor.authorSwan, BK
dc.contributor.authorLandry, ZC
dc.contributor.authorWoyke, T
dc.contributor.authorDeLong, EF
dc.contributor.authorStepanauskas, R
dc.contributor.authorGiovannoni, SJ
dc.date.accessioned2018-06-28T08:57:44Z
dc.date.issued2014-01-23
dc.description.abstractBacterioplankton of the SAR11 clade are the most abundant microorganisms in marine systems, usually representing 25% or more of the total bacterial cells in seawater worldwide. SAR11 is divided into subclades with distinct spatiotemporal distributions (ecotypes), some of which appear to be specific to deep water. Here we examine the genomic basis for deep ocean distribution of one SAR11 bathytype (depth-specific ecotype), subclade Ic. Four single-cell Ic genomes, with estimated completeness of 55%-86%, were isolated from 770 m at station ALOHA and compared with eight SAR11 surface genomes and metagenomic datasets. Subclade Ic genomes dominated metagenomic fragment recruitment below the euphotic zone. They had similar COG distributions, high local synteny and shared a large number (69%) of orthologous clusters with SAR11 surface genomes, yet were distinct at the 16S rRNA gene and amino-acid level, and formed a separate, monophyletic group in phylogenetic trees. Subclade Ic genomes were enriched in genes associated with membrane/cell wall/envelope biosynthesis and showed evidence of unique phage defenses. The majority of subclade Ic-specfic genes were hypothetical, and some were highly abundant in deep ocean metagenomic data, potentially masking mechanisms for niche differentiation. However, the evidence suggests these organisms have a similar metabolism to their surface counterparts, and that subclade Ic adaptations to the deep ocean do not involve large variations in gene content, but rather more subtle differences previously observed deep ocean genomic data, like preferential amino-acid substitutions, larger coding regions among SAR11 clade orthologs, larger intergenic regions and larger estimated average genome size.en_GB
dc.description.sponsorshipThis work was supported by the Gordon and Betty Moore Foundation (SJG and EFD), the US Department of Energy Joint Genome Institute (JGI) Community Supported Program grant 2011-387 (RS, BKS, EFD, SJG), National Science Foundation (NSF) Science and Technology Center Award EF0424599 (EFD), NSF awards EF-826924 (RS), OCE-821374 (RS) and OCE-1232982 (RS and BKS), and is based on work supported by the NSF under Award no. DBI-1003269 (JCT). Sequencing was conducted by JGI and supported by the Office of Science of the US Department of Energy under Contract No. DE-AC02-05CH11231.en_GB
dc.identifier.citationVol. 8, pp. 1440 - 1451en_GB
dc.identifier.doi10.1038/ismej.2013.243
dc.identifier.urihttp://hdl.handle.net/10871/33310
dc.language.isoenen_GB
dc.publisherNature Publishing Groupen_GB
dc.relation.urlhttps://www.ncbi.nlm.nih.gov/pubmed/24451205en_GB
dc.rights© 2014 International Society for Microbial Ecologyen_GB
dc.subjectAlphaproteobacteriaen_GB
dc.subjectDNA, Intergenicen_GB
dc.subjectEcotypeen_GB
dc.subjectGenes, rRNAen_GB
dc.subjectGenomicsen_GB
dc.subjectMetagenomeen_GB
dc.subjectPhylogenyen_GB
dc.subjectRNA, Ribosomal, 16Sen_GB
dc.subjectSeawateren_GB
dc.subjectSingle-Cell Analysisen_GB
dc.subjectSyntenyen_GB
dc.titleSingle-cell enabled comparative genomics of a deep ocean SAR11 bathytype.en_GB
dc.typeArticleen_GB
dc.date.available2018-06-28T08:57:44Z
dc.identifier.issn1751-7362
exeter.place-of-publicationEnglanden_GB
dc.descriptionThis is the author's accepted mansucript.en_GB
dc.descriptionFinal version available from Nature via the DOI in this record.en_GB
dc.identifier.journalISME Journalen_GB


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