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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/74889
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dc.contributor.authorBatista, Diego Felipe Alves-
dc.contributor.authorde Freitas Neto, Oliveiro Caetano-
dc.contributor.authorLopes, Priscila Diniz-
dc.contributor.authorde Almeida, Adriana Maria-
dc.contributor.authorBarrow Jr., Paul Andrew-
dc.contributor.authorBerchieri, Angelo-
dc.date.accessioned2014-05-27T11:28:44Z-
dc.date.accessioned2016-10-25T18:45:55Z-
dc.date.available2014-05-27T11:28:44Z-
dc.date.available2016-10-25T18:45:55Z-
dc.date.issued2013-03-28-
dc.identifierhttp://dx.doi.org/10.1177/1040638713479361-
dc.identifier.citationJournal of Veterinary Diagnostic Investigation, v. 25, n. 2, p. 259-262, 2013.-
dc.identifier.issn1040-6387-
dc.identifier.issn1943-4936-
dc.identifier.urihttp://hdl.handle.net/11449/74889-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/74889-
dc.description.abstractSalmonella Pullorum and Salmonella Gallinarum are classified as biovars of Salmonella enterica subsp. enterica serovar Gallinarum. These salmonellae are the causative agents of Pullorum disease and fowl typhoid, respectively, and are widely distributed throughout the world. Although many developed countries have eradicated these diseases from commercial poultry, they are still the cause of significant economic loss in developing countries. When serovar Gallinarum is isolated, it is difficult to immediately differentiate between biovars because they are antigenically identical by serotyping. However, they cause distinct diseases with different epidemiology, and therefore it is important to differentiate them. This may be done biochemically but takes 2 to 3 days. In the present study, S. Pullorum and S. Gallinarum whole genomes were compared, and 1 genomic region of difference, which is part of the ratA gene, was chosen as a molecular marker for a polymerase chain reaction assay to differentiate rapidly between these organisms. In all, 26 strains of S. Gallinarum and 17 S. Pullorum strains were tested and successfully differentiated by the assay. © 2013 The Author(s).en
dc.format.extent259-262-
dc.language.isoeng-
dc.sourceScopus-
dc.subjectGenome-
dc.subjectpolymerase chain reaction-
dc.subjectrapid differentiation-
dc.subjectratA gene-
dc.subjectSalmonella Gallinarum-
dc.subjectSalmonella Pullorum-
dc.subjectbacterial protein-
dc.subjectanimal-
dc.subjectanimal disease-
dc.subjectanimal salmonellosis-
dc.subjectbacterial genome-
dc.subjectbird disease-
dc.subjectclassification-
dc.subjectgene expression regulation-
dc.subjectgenetics-
dc.subjectmetabolism-
dc.subjectmicrobiology-
dc.subjectphysiology-
dc.subjectpoultry-
dc.subjectSalmonella enterica-
dc.subjectAnimals-
dc.subjectBacterial Proteins-
dc.subjectGene Expression Regulation, Bacterial-
dc.subjectGenome, Bacterial-
dc.subjectPolymerase Chain Reaction-
dc.subjectPoultry-
dc.subjectPoultry Diseases-
dc.subjectSalmonella Infections, Animal-
dc.titlePolymerase chain reaction assay based on ratA gene allows differentiation between Salmonella enterica subsp. enterica serovar Gallinarum biovars Gallinarum and Pullorumen
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.contributor.institutionUniversity of Nottingham-
dc.description.affiliationFaculty of Agriculture and Veterinary Sciences Universidade Estadual Paulista, Jaboticabal, São Paulo-
dc.description.affiliationSchool of Veterinary Medicine and Science University of Nottingham, Sutton Bonington, Leicestershire-
dc.description.affiliationUnespFaculty of Agriculture and Veterinary Sciences Universidade Estadual Paulista, Jaboticabal, São Paulo-
dc.identifier.doi10.1177/1040638713479361-
dc.identifier.wosWOS:000319220300013-
dc.rights.accessRightsAcesso restrito-
dc.identifier.file2-s2.0-84875309804.pdf-
dc.relation.ispartofJournal of Veterinary Diagnostic Investigation-
dc.identifier.scopus2-s2.0-84875309804-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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