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Detection of the agr System and Resistance to Antimicrobials in Biofilm-Producing S. epidermidis

dc.contributor.authorCataneli Pereira, Valéria [UNESP]
dc.contributor.authorPinheiro-Hubinger, Luiza [UNESP]
dc.contributor.authorde Oliveira, Adilson [UNESP]
dc.contributor.authorMoraes Riboli, Danilo Flávio [UNESP]
dc.contributor.authorBenini Martins, Katheryne [UNESP]
dc.contributor.authorCalixto Romero, Letícia [UNESP]
dc.contributor.authorRibeiro de Souza da Cunha, Maria de Lourdes [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionUNOESTE-University of West Paulista
dc.date.accessioned2021-06-25T10:46:44Z
dc.date.available2021-06-25T10:46:44Z
dc.date.issued2020-12-03
dc.description.abstractThe ability of Staphylococcus epidermidis to produce virulence factors, such as biofilm, added to its increased resistance to antimicrobials can cause infections that are difficult to treat. Many staphylococcal virulence factors are under the control of the accessory gene regulator (agr). The objective of this study was to establish the agr locus and susceptibility of biofilm-producing S. epidermidis specimens to antimicrobial agents, through PCR reactions, reverse transcription polymerase chain reaction (RT-PCR), and the determination of minimum inhibitory concentration (MIC), and to analyze the clonal profile of 300 strains isolated from blood culture specimens from inpatients at a University Hospital in Brazil, over a 20-year period by pulsed-field gel electrophoresis (PFGE) and multilocus sequence typing (MLST) techniques. The ica operon expression was shown in 83.6% strains, bhp gene in 11.5%, and aap gene in 32.8%. Oxacillin resistance was detected in 90.1%, while 4.9% showed tigecycline resistance, and intermediate resistance to quinupristin/dalfopristin was identified in 0.4%. Clonal profile determination showed 11 clusters, with the ST2 type determined as the major cluster. The S. epidermidis biofilm producer demonstrated a predominance of agr I locus, oxacillin resistance, and SCCmec III as well as the potential dissemination of pathogenic clones in hospital settings over long periods.en
dc.description.affiliationSector of Microbiology and Immunology Department of Chemical and Biological Sciences Institute of Biosciences UNESP-University Estadual Paulista
dc.description.affiliationSector of Microbiology and Immunology UNOESTE-University of West Paulista
dc.description.affiliationUnespSector of Microbiology and Immunology Department of Chemical and Biological Sciences Institute of Biosciences UNESP-University Estadual Paulista
dc.identifierhttp://dx.doi.org/10.3390/molecules25235715
dc.identifier.citationMolecules (Basel, Switzerland), v. 25, n. 23, 2020.
dc.identifier.doi10.3390/molecules25235715
dc.identifier.issn1420-3049
dc.identifier.scopus2-s2.0-85097483853
dc.identifier.urihttp://hdl.handle.net/11449/206958
dc.language.isoeng
dc.relation.ispartofMolecules (Basel, Switzerland)
dc.sourceScopus
dc.subjectagr locus
dc.subjectantimicrobial resistance
dc.subjectbiofilm
dc.subjectoxacillin resistance
dc.subjectST2
dc.titleDetection of the agr System and Resistance to Antimicrobials in Biofilm-Producing S. epidermidisen
dc.typeArtigopt
dspace.entity.typePublication
relation.isOrgUnitOfPublicationab63624f-c491-4ac7-bd2c-767f17ac838d
relation.isOrgUnitOfPublication.latestForDiscoveryab63624f-c491-4ac7-bd2c-767f17ac838d
unesp.author.orcid0000-0003-2080-9221 0000-0003-2080-9221[1]
unesp.author.orcid0000-0003-1343-6818[5]
unesp.author.orcid0000-0002-1787-704X[6]
unesp.author.orcid0000-0001-9079-2723[7]
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Biociências, Botucatupt
unesp.departmentMicrobiologia e Imunologia - IBBpt

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