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dc.contributor.authorDealtry, S
dc.contributor.authorDing, G-C
dc.contributor.authorWeichelt, V
dc.contributor.authorDunon, V
dc.contributor.authorSchlüter, A
dc.contributor.authorMartini, MC
dc.contributor.authorDel Papa, MF
dc.contributor.authorLagares, A
dc.contributor.authorAmos, GCA
dc.contributor.authorWellington, EMH
dc.contributor.authorGaze, WH
dc.contributor.authorSipkema, D
dc.contributor.authorSjöling, S
dc.contributor.authorSpringael, D
dc.contributor.authorHeuer, H
dc.contributor.authorvan Elsas, JD
dc.contributor.authorThomas, C
dc.contributor.authorSmalla, K
dc.date.accessioned2017-03-08T11:16:44Z
dc.date.issued2014-02-24
dc.description.abstractIncP-1, IncP-7 and IncP-9 plasmids often carry genes encoding enzymes involved in the degradation of man-made and natural contaminants, thus contributing to bacterial survival in polluted environments. However, the lack of suitable molecular tools often limits the detection of these plasmids in the environment. In this study, PCR followed by Southern blot hybridization detected the presence of plasmid-specific sequences in total community (TC-) DNA or fosmid DNA from samples originating from different environments and geographic regions. A novel primer system targeting IncP-9 plasmids was developed and applied along with established primers for IncP-1 and IncP-7. Screening TC-DNA from biopurification systems (BPS) which are used on farms for the purification of pesticide-contaminated water revealed high abundances of IncP-1 plasmids belonging to different subgroups as well as IncP-7 and IncP-9. The novel IncP-9 primer-system targeting the rep gene of nine IncP-9 subgroups allowed the detection of a high diversity of IncP-9 plasmid specific sequences in environments with different sources of pollution. Thus polluted sites are "hot spots" of plasmids potentially carrying catabolic genes.en_GB
dc.description.sponsorshipThis study was funded by the EU 7th Framework Programme (MetaExplore 222625) and the Inter-University Attraction Pole (IUAP) “µ-manager” of the Belgian Science Policy (BELSPO, P7/25). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.en_GB
dc.identifier.citationVol. 9 (2), article e89922en_GB
dc.identifier.doi10.1371/journal.pone.0089922
dc.identifier.urihttp://hdl.handle.net/10871/26323
dc.language.isoenen_GB
dc.publisherPublic Library of Scienceen_GB
dc.relation.urlhttps://www.ncbi.nlm.nih.gov/pubmed/24587126en_GB
dc.rightsCopyright: © 2014 Dealtry et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License(https://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.en_GB
dc.subjectAnimalsen_GB
dc.subjectBase Sequenceen_GB
dc.subjectBlotting, Southernen_GB
dc.subjectDNA Primersen_GB
dc.subjectDNA, Bacterialen_GB
dc.subjectEnvironmental Pollutantsen_GB
dc.subjectEuropeen_GB
dc.subjectGenetic Variationen_GB
dc.subjectMolecular Sequence Dataen_GB
dc.subjectPlasmidsen_GB
dc.subjectPolymerase Chain Reactionen_GB
dc.subjectPoriferaen_GB
dc.subjectRNA, Ribosomal, 16Sen_GB
dc.subjectSequence Analysis, DNAen_GB
dc.titleCultivation-independent screening revealed hot spots of IncP-1, IncP-7 and IncP-9 plasmid occurrence in different environmental habitatsen_GB
dc.typeArticleen_GB
dc.date.available2017-03-08T11:16:44Z
exeter.place-of-publicationUnited Statesen_GB
dc.descriptionThis is the final version of the article. Available from Public Library of Science via the DOI in this record.en_GB
dc.identifier.journalPLoS Oneen_GB


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