Please use this identifier to cite or link to this item: https://hdl.handle.net/10316/109267
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dc.contributor.authorFigueiredo, Rui-
dc.contributor.authorCard, Roderick-
dc.contributor.authorNunes, Carla-
dc.contributor.authorAbuOun, Manal-
dc.contributor.authorBagnall, Mary C.-
dc.contributor.authorNunez, Javier-
dc.contributor.authorMendonça, Nuno-
dc.contributor.authorAnjum, Muna F.-
dc.contributor.authorSilva, Gabriela Jorge da-
dc.date.accessioned2023-10-06T10:14:20Z-
dc.date.available2023-10-06T10:14:20Z-
dc.date.issued2015-
dc.identifier.issn1932-6203pt
dc.identifier.urihttps://hdl.handle.net/10316/109267-
dc.description.abstractSalmonella enterica is a zoonotic foodborne pathogen that causes acute gastroenteritis in humans. We assessed the virulence potential of one-hundred and six Salmonella strains isolated from food animals and products. A high through-put virulence genes microarray demonstrated Salmonella Pathogenicity Islands (SPI) and adherence genes were highly conserved, while prophages and virulence plasmid genes were variably present. Isolates were grouped by serotype, and virulence plasmids separated S. Typhimurium in two clusters. Atypical microarray results lead to whole genome sequencing (WGS) of S. Infantis Sal147, which identified deletion of thirty-eight SPI-1 genes. Sal147 was unable to invade HeLa cells and showed reduced mortality in Galleria mellonella infection model, in comparison to a SPI-1 harbouring S. Infantis. Microarray and WGS of S. Typhimurium Sal199, established for the first time in S. Typhimurium presence of cdtB and other Typhi-related genes. Characterization of Sal199 showed cdtB genes were upstream of transposase IS911, and co-expressed with other Typhi-related genes. Cell cycle arrest, cytoplasmic distension, and nuclear enlargement were detected in HeLa cells infected by Sal199, but not with S. Typhimurium LT2. Increased mortality of Galleria was detected on infection with Sal199 compared to LT2. Thus, Salmonella isolates were rapidly characterized using a high through-put microarray; helping to identify unusual virulence features which were corroborated by further characterisation. This work demonstrates that the use of suitable screening methods for Salmonella virulence can help assess the potential risk associated with certain Salmonella to humans. Incorporation of such methodology into surveillance could help reduce the risk of emergence of epidemic Salmonella strains.pt
dc.description.sponsorshipThis work was supported financially by the project PTDC/AGR-ALI/113953/2009 from Fundação para a Ciência e Tecnologia and by PEst-OE/SAU/ UI0177/2014 of the Center for Pharmaceutical Studies, University of Coimbra, Portugal. Rui Figueiredo was supported by grant SFRH/BD/78833/ 2011, and Nuno Mendonça by the grant from SFRH/ BPD/45815/2008 from Fundação para a Ciência e Tecnologia. Work undertaken at the Animal and Plant Health Agency was funded by the UK government Department for Environment, Food and Rural Affairs.pt
dc.language.isoengpt
dc.publisherPublic Library of Sciencept
dc.rightsopenAccesspt
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/pt
dc.subject.meshAnimalspt
dc.subject.meshBacterial Toxinspt
dc.subject.meshGene Expression Regulation, Bacterialpt
dc.subject.meshGenome, Bacterialpt
dc.subject.meshGenomic Islandspt
dc.subject.meshHT29 Cellspt
dc.subject.meshHeLa Cellspt
dc.subject.meshHost-Pathogen Interactionspt
dc.subject.meshHumanspt
dc.subject.meshMothspt
dc.subject.meshOligonucleotide Array Sequence Analysispt
dc.subject.meshPlasmidspt
dc.subject.meshReproducibility of Resultspt
dc.subject.meshReverse Transcriptase Polymerase Chain Reactionpt
dc.subject.meshSalmonella Infections, Animalpt
dc.subject.meshSalmonella entericapt
dc.subject.meshSalmonella typhimuriumpt
dc.subject.meshSerotypingpt
dc.subject.meshSpecies Specificitypt
dc.subject.meshVirulencept
dc.titleVirulence Characterization of Salmonella enterica by a New Microarray: Detection and Evaluation of the Cytolethal Distending Toxin Gene Activity in the Unusual Host S. Typhimuriumpt
dc.typearticle-
degois.publication.firstPagee0135010pt
degois.publication.issue8pt
degois.publication.titlePLoS ONEpt
dc.peerreviewedyespt
dc.identifier.doi10.1371/journal.pone.0135010pt
degois.publication.volume10pt
dc.date.embargo2015-01-01*
uc.date.periodoEmbargo0pt
item.languageiso639-1en-
item.openairetypearticle-
item.grantfulltextopen-
item.fulltextCom Texto completo-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
crisitem.author.researchunitMARE - Marine and Environmental Sciences Centre-
crisitem.author.researchunitCNC - Center for Neuroscience and Cell Biology-
crisitem.author.orcid0000-0002-5567-282X-
crisitem.author.orcid0000-0002-7479-8540-
Appears in Collections:I&D CNC - Artigos em Revistas Internacionais
FFUC- Artigos em Revistas Internacionais
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