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dc.date.accessioned2017-08-08T09:23:57Z
dc.date.available2017-08-08T09:23:57Z
dc.date.created2015-02-10T19:38:45Z
dc.date.issued2014
dc.identifier.citationde Been, Mark Lanza, Val F. de Toro, Maria Scharringa, Jelle Dohmen, Wietske Du, Yu Hu, Juan Lei, Ying Li, Ning Tooming-Klunderud, Ave Heederik, Dick J. J. Fluit, Ad C Bonten, Marc J M Willems, Rob J.L. de la Cruz, Fernando van Schaik, Willem . Dissemination of Cephalosporin Resistance Genes between Escherichia coli Strains from Farm Animals and Humans by Specific Plasmid Lineages. PLoS Genetics. 2014, 10(12)
dc.identifier.urihttp://hdl.handle.net/10852/56838
dc.description.abstractThird-generation cephalosporins are a class of β-lactam antibiotics that are often used for the treatment of human infections caused by Gram-negative bacteria, especially Escherichia coli. Worryingly, the incidence of human infections caused by third-generation cephalosporin-resistant E. coli is increasing worldwide. Recent studies have suggested that these E. coli strains, and their antibiotic resistance genes, can spread from food-producing animals, via the food-chain, to humans. However, these studies used traditional typing methods, which may not have provided sufficient resolution to reliably assess the relatedness of these strains. We therefore used whole-genome sequencing (WGS) to study the relatedness of cephalosporin-resistant E. coli from humans, chicken meat, poultry and pigs. One strain collection included pairs of human and poultry-associated strains that had previously been considered to be identical based on Multi-Locus Sequence Typing, plasmid typing and antibiotic resistance gene sequencing. The second collection included isolates from farmers and their pigs. WGS analysis revealed considerable heterogeneity between human and poultry-associated isolates. The most closely related pairs of strains from both sources carried 1263 Single-Nucleotide Polymorphisms (SNPs) per Mbp core genome. In contrast, epidemiologically linked strains from humans and pigs differed by only 1.8 SNPs per Mbp core genome. WGS-based plasmid reconstructions revealed three distinct plasmid lineages (IncI1- and IncK-type) that carried cephalosporin resistance genes of the Extended-Spectrum Beta-Lactamase (ESBL)- and AmpC-types. The plasmid backbones within each lineage were virtually identical and were shared by genetically unrelated human and animal isolates. Plasmid reconstructions from short-read sequencing data were validated by long-read DNA sequencing for two strains. Our findings failed to demonstrate evidence for recent clonal transmission of cephalosporin-resistant E. coli strains from poultry to humans, as has been suggested based on traditional, low-resolution typing methods. Instead, our data suggest that cephalosporin resistance genes are mainly disseminated in animals and humans via distinct plasmids.en_US
dc.languageEN
dc.publisherPublic Library of Science (PLoS)
dc.rightsAttribution 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.titleDissemination of Cephalosporin Resistance Genes between Escherichia coli Strains from Farm Animals and Humans by Specific Plasmid Lineagesen_US
dc.typeJournal articleen_US
dc.creator.authorde Been, Mark
dc.creator.authorLanza, Val F.
dc.creator.authorde Toro, Maria
dc.creator.authorScharringa, Jelle
dc.creator.authorDohmen, Wietske
dc.creator.authorDu, Yu
dc.creator.authorHu, Juan
dc.creator.authorLei, Ying
dc.creator.authorLi, Ning
dc.creator.authorTooming-Klunderud, Ave
dc.creator.authorHeederik, Dick J. J.
dc.creator.authorFluit, Ad C
dc.creator.authorBonten, Marc J M
dc.creator.authorWillems, Rob J.L.
dc.creator.authorde la Cruz, Fernando
dc.creator.authorvan Schaik, Willem
cristin.unitcode185,15,29,50
cristin.unitnameCentre for Ecological and Evolutionary Synthesis
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.fulltextoriginal
cristin.qualitycode2
dc.identifier.cristin1219848
dc.identifier.bibliographiccitationinfo:ofi/fmt:kev:mtx:ctx&ctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=PLoS Genetics&rft.volume=10&rft.spage=&rft.date=2014
dc.identifier.jtitlePLoS Genetics
dc.identifier.volume10
dc.identifier.issue12
dc.identifier.pagecount17
dc.identifier.doihttp://dx.doi.org/10.1371/journal.pgen.1004776
dc.identifier.urnURN:NBN:no-59665
dc.type.documentTidsskriftartikkelen_US
dc.type.peerreviewedPeer reviewed
dc.source.issn1553-7390
dc.identifier.fulltextFulltext https://www.duo.uio.no/bitstream/handle/10852/56838/1/journal.pgen.1004776.pdf
dc.type.versionPublishedVersion
cristin.articleide1004776


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