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dc.contributor.authorBetancor, Laura-
dc.contributor.authorYim, Lucia-
dc.contributor.authorFookes, Maria-
dc.contributor.authorMartinez, Araci-
dc.contributor.authorThomson, Nicholas R-
dc.contributor.authorIvens, Alasdair-
dc.contributor.authorPeters, Sarah-
dc.contributor.authorBryant, Clare-
dc.contributor.authorAlgorta, Gabriela-
dc.contributor.authorKariuki, Samuel-
dc.contributor.authorSchelotto, Felipe-
dc.contributor.authorMaskell, Duncan-
dc.contributor.authorDougan, Gordon-
dc.contributor.authorChabalgoity, Jose A-
dc.date.accessioned2026-05-28T12:17:16Z-
dc.date.available2026-05-28T12:17:16Z-
dc.date.issued2009-
dc.identifier.citationBETANCOR, L., YIM, L., FOOKES, M., y otros. Genomic and phenotypic variation in epidemic-spanning Salmonella enterica serovar Enteritidis isolates. BMC Microbiol [en línea] 2009, 9. DOI: 10.1186/1471-2180-9-237es
dc.identifier.urihttps://hdl.handle.net/20.500.12008/55240-
dc.description.abstractBackground: Salmonella enterica serovar Enteritidis (S. Enteritidis) has caused major epidemics of gastrointestinal infection in many different countries. In this study we investigate genome divergence and pathogenic potential in S. Enteritidis isolated before, during and after an epidemic in Uruguay. Results: 266 S. Enteritidis isolates were genotyped using RAPD-PCR and a selection were subjected to PFGE analysis. From these, 29 isolates spanning different periods, genetic profiles and sources of isolation were assayed for their ability to infect human epithelial cells and subjected to comparative genomic hybridization using a Salmonella pan-array and the sequenced strain S. Enteritidis PT4 P125109 as reference. Six other isolates from distant countries were included as external comparators. Two hundred and thirty three chromosomal genes as well as the virulence plasmid were found as variable among S. Enteritidis isolates. Ten out of the 16 chromosomal regions that varied between different isolates correspond to phage-like regions. The 2 oldest pre-epidemic isolates lack phage SE20 and harbour other phage encoded genes that are absent in the sequenced strain. Besides variation in prophage, we found variation in genes involved in metabolism and bacterial fitness. Five epidemic strains lack the complete Salmonella virulence plasmid. Significantly, strains with indistinguishable genetic patterns still showed major differences in their ability to infect epithelial cells, indicating that the approach used was insufficient to detect the genetic basis of this differential behaviour. Conclusion: The recent epidemic of S. Enteritidis infection in Uruguay has been driven by the introduction of closely related strains of phage type 4 lineage. Our results confirm previous reports demonstrating a high degree of genetic homogeneity among S. Enteritidis isolates. However, 10 of the regions of variability described here are for the first time reported as being variable in S. Enteritidis. In particular, the oldest pre-epidemic isolates carry phage-associated genetic regions not previously reported in S. Enteritidis. Overall, our results support the view that phages play a crucial role in the generation of genetic diversity in S. Enteritidis and that phage SE20 may be a key marker for the emergence of particular isolates capable of causing epidemics.es
dc.format.mimetypeapplication/pdfes
dc.language.isoenes
dc.relation.ispartofBMC Microbiol. 9, 2009es
dc.rightsLas obras depositadas en el Repositorio se rigen por la Ordenanza de los Derechos de la Propiedad Intelectual de la Universidad de la República.(Res. Nº 91 de C.D.C. de 8/III/1994 – D.O. 7/IV/1994) y por la Ordenanza del Repositorio Abierto de la Universidad de la República (Res. Nº 16 de C.D.C. de 07/10/2014)es
dc.subject.otherSALMONELLA ENTERITIDISes
dc.subject.otherPHENOTYPEes
dc.subject.otherGENOMICSes
dc.titleGenomic and phenotypic variation in epidemic-spanning Salmonella enterica serovar Enteritidis isolateses
dc.typeArtículoes
dc.contributor.filiacionBetancor Laura, Universidad de la República (Uruguay). Facultad de Medicina. Instituto de Higiene. Unidad Académica Desarrollo Biotecnológico-
dc.contributor.filiacionYim Lucia, Universidad de la República (Uruguay). Facultad de Medicina. Instituto de Higiene. Unidad Académica Desarrollo Biotecnológico-
dc.contributor.filiacionFookes Maria, Wellcome Trust Genome Campus (Reino Unido). The Wellcome Trust Sanger Institute-
dc.contributor.filiacionMartinez Araci, Universidad de la República (Uruguay). Facultad de Medicina. Instituto de Higiene. Unidad Académica Bacteriología y Virología-
dc.contributor.filiacionThomson Nicholas R, Wellcome Trust Genome Campus (Reino Unido). The Wellcome Trust Sanger Institute-
dc.contributor.filiacionIvens Alasdair, Wellcome Trust Genome Campus (Reino Unido). The Wellcome Trust Sanger Institute-
dc.contributor.filiacionPeters Sarah, University of Cambridge (Reino Unido). Department of Veterinary Medicine-
dc.contributor.filiacionBryant Clare, University of Cambridge (Reino Unido). Department of Veterinary Medicine-
dc.contributor.filiacionAlgorta Gabriela, Universidad de la República (Uruguay). Facultad de Medicina. Instituto de Higiene. Unidad Académica Bacteriología y Virología-
dc.contributor.filiacionKariuki Samuel, Kenya Medical Research Institute (Kenia). Centre for Microbiology Research-
dc.contributor.filiacionSchelotto Felipe, Universidad de la República (Uruguay). Facultad de Medicina. Instituto de Higiene. Unidad Académica Bacteriología y Virología-
dc.contributor.filiacionMaskell Duncan, University of Cambridge (Reino Unido). Department of Veterinary Medicine-
dc.contributor.filiacionDougan Gordon, Wellcome Trust Genome Campus (Reino Unido). The Wellcome Trust Sanger Institute-
dc.contributor.filiacionChabalgoity Jose A, Universidad de la República (Uruguay). Facultad de Medicina. Instituto de Higiene. Unidad Académica Desarrollo Biotecnológico-
dc.rights.licenceLicencia Creative Commons Atribución (CC - By 4.0)es
dc.identifier.doi10.1186/1471-2180-9-237-
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