Please use this identifier to cite or link to this item: https://scholarhub.balamand.edu.lb/handle/uob/2495
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dc.contributor.authorDeguenon, Estheren_US
dc.contributor.authorDougnon, Victorienen_US
dc.contributor.authorLozes, Evelyneen_US
dc.contributor.authorMaman, Nanaen_US
dc.contributor.authorAbdel-Massih, Roulaen_US
dc.date.accessioned2020-12-23T09:14:26Z-
dc.date.available2020-12-23T09:14:26Z-
dc.date.issued2019-
dc.identifier.urihttps://scholarhub.balamand.edu.lb/handle/uob/2495-
dc.description.abstractOBJECTIVE: Salmonella spp. are one of the leading foodborne pathogens worldwide naturally found in the intestines of many animals. People that are in direct contact with the infected animals or their cages may become ill. The aim of this study was to determine the prevalence, antibiogram and virulence genes associated with Salmonella serovars from fecal samples of animals intended for consumption in Southern Benin. RESULTS: Out of a total of 406 samples, 2.46% were positive. The isolates identified were multidrug-resistant Salmonella spp. to penicillins, first generation cephalosporins and some aminoglycosides. All Salmonella isolates produced invA gene of 284 bp, fimA of 85 bp and stn of 260 bp. The spvC gene (571 bp) was present in 10% of the isolates whereas the spvR gene (310 bp) was found in 20% of the isolates. The control strain possessed all the tested genes. The invA gene implies that strains are able to invade epithelial cells. The fimA and stn genes present in all isolates show that they are capable of causing gastrointestinal illness in humans. The presence of spvC and spvR genes suggests the possibility of these strains to produce toxins.en_US
dc.language.isoengen_US
dc.subjectVirulence genesen_US
dc.subject.lcshSalmonellaen_US
dc.subject.lcshMultidrug resistanceen_US
dc.titleResistance and virulence determinants of faecal Salmonella spp. isolated from slaughter animals in Beninen_US
dc.typeJournal Articleen_US
dc.contributor.affiliationDepartment of Biologyen_US
dc.description.volume12en_US
dc.description.issue317en_US
dc.description.startpage1en_US
dc.description.endpage7en_US
dc.date.catalogued2019-09-04-
dc.description.statusPublisheden_US
dc.identifier.OlibID198562-
dc.identifier.openURLhttps://bmcresnotes.biomedcentral.com/track/pdf/10.1186/s13104-019-4341-xen_US
dc.relation.ispartoftextBiomedical central research notes (BMC)en_US
dc.provenance.recordsourceOliben_US
Appears in Collections:Department of Biology
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