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dc.contributor.authorWarwick-Dugdale, J
dc.contributor.authorSolonenko, N
dc.contributor.authorMoore, K
dc.contributor.authorChittick, L
dc.contributor.authorGregory, AC
dc.contributor.authorAllen, M
dc.contributor.authorSullivan, MB
dc.contributor.authorTemperton, B
dc.date.accessioned2019-03-19T09:30:47Z
dc.date.issued2019-04-25
dc.description.abstractMarine viruses impact global biogeochemical cycles via their influence on host community structure and function, yet our understanding of viral ecology is constrained by limitations in host culturing and a lack of reference genomes and ‘universal’ gene markers to facilitate community surveys. Short-read viral metagenomic studies have provided clues to viral function and first estimates of global viral gene abundance and distribution, but their assemblies are confounded by populations with high levels of strain evenness and nucleotide diversity (microdiversity), limiting assembly of some of the most abundant viruses on Earth. Such features also challenge assembly across genomic islands containing niche-defining genes that drive ecological speciation. These populations and features may be successfully captured by single-virus genomics and fosmid-based approaches, at least in abundant taxa, but at considerable cost and technical expertise. Here we established a low-cost, low-input, high throughput alternative sequencing and informatics workflow to improve viral metagenomic assemblies using short-read and long-read technology. The ‘VirION’ (Viral, long-read metagenomics via MinION sequencing) approach was first validated using mock communities where it was found to be as relatively quantitative as short-read methods and provided significant improvements in recovery of viral genomes. We then then applied VirION to the first metagenome from a natural viral community from the Western English Channel. In comparison to a short-read only approach, VirION: (i) increased number and completeness of assembled viral genomes; (ii) captured abundant, highly microdiverse virus populations, and (iii) captured more and longer genomic islands. Together, these findings suggest that VirION provides a high throughput and cost-effective alternative to fosmid and singlevirus genomic approaches to more comprehensively explore viral communities in nature.en_GB
dc.description.sponsorshipNatural Environment Research Council (NERC)en_GB
dc.description.sponsorshipRoyal Society (Charity)en_GB
dc.description.sponsorshipSimons Foundationen_GB
dc.identifier.citationPublished online 25 April 2019en_GB
dc.identifier.doi10.7717/peerj.6800
dc.identifier.urihttp://hdl.handle.net/10871/36565
dc.language.isoenen_GB
dc.publisherPeerJ Inc.en_GB
dc.titleLong-read viral metagenomics captures abundant and microdiverse viral populations and their niche-defining genomic islandsen_GB
dc.typeArticleen_GB
dc.date.available2019-03-19T09:30:47Z
dc.identifier.issn2167-8359
dc.descriptionThis is the final version. Available on open access from PeerJ via the DOI in this recorden_GB
dc.identifier.journalPeerJen_GB
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/en_GB
dcterms.dateAccepted2019-03-14
exeter.funder::Natural Environment Research Council (NERC)en_GB
exeter.funder::Natural Environment Research Council (NERC)en_GB
exeter.funder::Royal Society (Charity)en_GB
exeter.funder::Simons Foundationen_GB
rioxxterms.versionvoRen_GB
rioxxterms.licenseref.startdate2019-03-18
rioxxterms.typeJournal Article/Reviewen_GB
refterms.dateFCD2019-03-19T09:17:22Z
refterms.versionFCDAM
refterms.dateFOA2019-05-14T10:59:16Z
refterms.panelAen_GB


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