Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/644
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dc.contributor.authorAdzitey, F.-
dc.contributor.authorDeli, R. A.-
dc.contributor.authorAli, G. R. R.-
dc.date.accessioned2016-06-30T16:40:11Z-
dc.date.available2016-06-30T16:40:11Z-
dc.date.issued2015-
dc.identifier.issn1684-1182-
dc.identifier.urihttp://hdl.handle.net/123456789/644-
dc.description.abstractThe objective of this study was to characterize Salmonella Typhimurium, Salmonella Enteritidis and Salmonella Albany strains isolated from chicken and ducks to determine their relatedness using Random Amplified Polymorphic Deoxyribonucleic Acid (RAPD)-PCR. RAPD-PCR analysis of the Salmonella serovars produced DNA bands that ranged from 242 to 3189bp for Salmonella Typhimurium, 252 to 2756bp for Salmonella Enteritidis and 232 to 2612 bp for Salmonella Albany. Cluster analysis at a coefficient of 0.85 grouped the Salmonella serovars into various clusters and singletons. Salmonella Typhimurium were grouped into 4 clusters and 1 singleton at a discriminatory index of 0.85.Salmonella Enteritidis were grouped into 2 clusters and 2 singletons at a discriminatory index of 0.64. Salmonella Albany were grouped into 3 clusters and 1 singleton at a discriminatory index of 0.71. One Salmonella Typhimurium isolated from chicken carcass was not characterized as the RAPD-PCR employed failed to produce any DNA band from that isolate. Characterizing Salmonella serovars from different sources is important to determine their genetic relatedness, and source of contamination and spreaden_US
dc.language.isoenen_US
dc.publisherJakraya Publications (P) Ltd.en_US
dc.relation.ispartofseriesVol. 2;-
dc.subjectChickenen_US
dc.subjectDucksen_US
dc.subjectSalmonella albanyen_US
dc.subjectSalmonella enteritidisen_US
dc.subjectSalmonella typhimuriumen_US
dc.subjectRAPD-PCen_US
dc.titleCHARACTERIZATION OF SALMONELLA TYPHIMURIUM, SALMONELLA ENTERITIDIS AND SALMONELLA ALBANY ISOLATED FROM CHICKENS AND DUCKS USING RANDOM AMPLIFIED POLYMORPHIC DNA (RAPD)-PCRFen_US
dc.typeArticleen_US
Appears in Collections:Faculty of Agriculture, Food and Consumer Sciences



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