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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/69631
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dc.contributor.authorCunha, Maria de Lourdes R. S. da-
dc.contributor.authorCalsolari, Regina A. O.-
dc.contributor.authorAraújo Jr., João Pessoa-
dc.date.accessioned2014-05-27T11:22:27Z-
dc.date.accessioned2016-10-25T18:23:47Z-
dc.date.available2014-05-27T11:22:27Z-
dc.date.available2016-10-25T18:23:47Z-
dc.date.issued2007-04-30-
dc.identifierhttp://dx.doi.org/10.1111/j.1348-0421.2007.tb03925.x-
dc.identifier.citationMicrobiology and Immunology, v. 51, n. 4, p. 381-390, 2007.-
dc.identifier.issn0385-5600-
dc.identifier.issn1348-0421-
dc.identifier.urihttp://hdl.handle.net/11449/69631-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/69631-
dc.description.abstractThe detection of staphylococcal enterotoxins is decisive for the confirmation of an outbreak and for the determination of the enterotoxigenicity of strains. Since the recognition of their antigenicity, a large number of serological methods for the detection of enterotoxins in food and culture media have been proposed. Since immunological methods require detectable amounts of toxin, molecular biology techniques represent important tools in the microbiology laboratory. In the present study, polymerase chain reaction (PCR) was used to identify genes responsible for the production of enterotoxins and toxic shock syndrome toxin 1 (TSST-1) in S. aureus and coagulase-negative staphylococci (CNS) isolated from patients and the results were compared with those obtained by the reverse passive latex agglutination (RPLA) assay. PCR detection of toxin genes revealed a higher percentage of toxigenic S. aureus strains (46.7%) than the RPLA method (38.3%). Analysis of the toxigenic profile of CNS strains showed that 26.7% of the isolates produced some type of toxin, and one or more toxin-specific genes were detected in 40% of the isolates. These results suggests the need for further studies in order to better characterize the pathogenic potential of CNS and indicate that attention should be paid to the toxigenic capacity of this group of microorganisms.en
dc.format.extent381-390-
dc.language.isoeng-
dc.sourceScopus-
dc.subjectCoagulase-negative staphylococci-
dc.subjectEnterotoxins-
dc.subjectPCR-
dc.subjectTSST-1-
dc.subjectcoagulase-
dc.subjectenterotoxin-
dc.subjecttoxic shock syndrome toxin 1-
dc.subjectagglutination test-
dc.subjectbacterial strain-
dc.subjectgene identification-
dc.subjectnonhuman-
dc.subjectpolymerase chain reaction-
dc.subjectStaphylococcus-
dc.subjectStaphylococcus aureus-
dc.subjectStaphylococcus epidermidis-
dc.subjectStaphylococcus haemolyticus-
dc.subjectStaphylococcus hominis-
dc.subjectStaphylococcus lugdunensis-
dc.subjectStaphylococcus simulans-
dc.subjectstaphylococcus warneri-
dc.subjectStaphylococcus xylosus-
dc.subjecttoxin analysis-
dc.subjectCoagulase-
dc.subjectNucleic Acid Hybridization-
dc.subjectPolymerase Chain Reaction-
dc.subjectStaphylococcal Infections-
dc.titleDetection of enterotoxin and toxic shock syndrome toxin 1 genes in Staphylococcus, with emphasis on coagulase-negative staphylococcien
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.description.affiliationDepartamento de Microbiologia e Imunologia Instituto de Biociências Universidade Estadual Paulista, Botucatu, SP-
dc.description.affiliationDepartamento de Microbiologia e Imunologia Instituto de Biociências Universidade Estadual Paulista, Caixa Postal 510, Botucatu, SP, CEP 18618-000-
dc.description.affiliationUnespDepartamento de Microbiologia e Imunologia Instituto de Biociências Universidade Estadual Paulista, Botucatu, SP-
dc.description.affiliationUnespDepartamento de Microbiologia e Imunologia Instituto de Biociências Universidade Estadual Paulista, Caixa Postal 510, Botucatu, SP, CEP 18618-000-
dc.identifier.doi10.1111/j.1348-0421.2007.tb03925.x-
dc.identifier.wosWOS:000245474900004-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofMicrobiology and Immunology-
dc.identifier.scopus2-s2.0-34247375584-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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