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Virulence properties and antimicrobial susceptibility of Shiga toxin-producing Escherichia coli strains isolated from healthy cattle from Parana State, Brazil

dc.contributor.authorPigatto, Caroline P. [UNESP]
dc.contributor.authorSchocken-Iturrino, Ruben P. [UNESP]
dc.contributor.authorSouza, Emanuel M.
dc.contributor.authorPedrosa, Fabio O.
dc.contributor.authorComarella, Larissa
dc.contributor.authorIrino, Kinue
dc.contributor.authorKato, Maria Aide M. F.
dc.contributor.authorFarah, Sonia M. S. S.
dc.contributor.authorWarth, Jose F.
dc.contributor.authorFadel-Picheth, Cyntia M. T.
dc.contributor.institutionUniversidade Federal do Paraná (UFPR)
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionAdolfo Inst
dc.contributor.institutionCent Lab Parana
dc.date.accessioned2014-05-20T13:16:02Z
dc.date.available2014-05-20T13:16:02Z
dc.date.issued2008-07-01
dc.description.abstractThe presence of Shiga toxin-producing Escherichia coli (STEC) strains in feces samples of cattle was determined using the cytotoxicity assay on Vero cells and a screening PCR system to detect stx genes. The STEC isolates were sero-typed, tested for antimicrobial Susceptibility, and analyzed for virulence genes using multiplex PCR. The verocytotoxin-producing E. coli - reverse passive latex agglutination (VTEC-RPLA) assay was also used to detect Shiga toxin production. The frequency of cattle shedding STEC was 36%. The isolates belonged to 33 different serotypes. of which O10:H42, O98:H41, and O159:H21 had not previously been associated with STEC. The most frequent serotypes were ONT:H7 (10%), O22:H8 (7%) O22:H16 (7%), and ONT:H21 (7%). Most of the strains (96%) were susceptible to all antimicrobial agents tested. Shiga toxin was detected by the VTEC-RPLA assay in most (89%) of the STEC strains. The frequency of virulence markers was as follows: stx(1), 10%; stx(2), 43%; stx(1), plus stx(2), 47%; ehxA, 44%; eae, 1%; and saa, 38%. Several strains belong to serotypes associated with human disease, and most of them carried a stx(2)-type gene, suggesting that they represent a risk to human health. The screening PCR assay showed fewer false-negative results for STEC than the Vero-cell assay and is suitable for laboratory routine.en
dc.description.affiliationUniversidade Federal do Paraná (UFPR), Dept Med Pathol, BR-80210170 Curitiba, PR, Brazil
dc.description.affiliationUniversidade Federal do Paraná (UFPR), Dept Vet Med, BR-80035050 Curitiba, Parana, Brazil
dc.description.affiliationUniversidade Federal do Paraná (UFPR), Dept Med Pathol, BR-80210170 Curitiba, Parana, Brazil
dc.description.affiliationSão Paulo State Univ UNESP, Dept Vet Pathol, BR-14884900 Jaboticabal, SP, Brazil
dc.description.affiliationAdolfo Inst, BR-01246902 São Paulo, Brazil
dc.description.affiliationUniversidade Federal do Paraná (UFPR), Dept Biochem & Mol Biol, Ctr Politecn, BR-81531990 Curitiba, PR, Brazil
dc.description.affiliationCent Lab Parana, Sao Jose Dos Pinhais, PR, Brazil
dc.description.affiliationUnespSão Paulo State Univ UNESP, Dept Vet Pathol, BR-14884900 Jaboticabal, SP, Brazil
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
dc.description.sponsorshipCoordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)
dc.format.extent588-593
dc.identifierhttp://dx.doi.org/10.1139/W08-046
dc.identifier.citationCanadian Journal of Microbiology. Ottawa: Natl Research Council Canada-n R C Research Press, v. 54, n. 7, p. 588-593, 2008.
dc.identifier.dimensionspub.1004420702
dc.identifier.doi10.1139/W08-046
dc.identifier.issn0008-4166
dc.identifier.issn1480-3275
dc.identifier.orcid0000-0003-3408-2633
dc.identifier.orcid0000-0003-1546-9218
dc.identifier.orcid0000-0002-0478-6544
dc.identifier.pmid18641705
dc.identifier.urihttp://hdl.handle.net/11449/3008
dc.identifier.wosWOS:000258504800009
dc.language.isoeng
dc.publisherNatl Research Council Canada-n R C Research Press
dc.publisherCanadian Science Publishing
dc.relation.ispartofCanadian Journal of Microbiology
dc.relation.ispartofjcr1.243
dc.relation.ispartofsjr0,579
dc.rights.accessRightsAcesso restritopt
dc.sourceWeb of Science
dc.sourceDimensions
dc.subjectSTECen
dc.subjectstx genesen
dc.subjectVirulence genesen
dc.subjectShiga toxinen
dc.subjectantimicrobial susceptibilityen
dc.titleVirulence properties and antimicrobial susceptibility of Shiga toxin-producing Escherichia coli strains isolated from healthy cattle from Parana State, Brazilen
dc.typeArtigopt
dcterms.licensehttp://www.nrcresearchpress.com/page/authors/information/rights
dcterms.rightsHolderNatl Research Council Canada-n R C Research Press
dspace.entity.typePublication
relation.isOrgUnitOfPublication3d807254-e442-45e5-a80b-0f6bf3a26e48
relation.isOrgUnitOfPublication.latestForDiscovery3d807254-e442-45e5-a80b-0f6bf3a26e48
unesp.author.orcid0000-0003-3408-2633[2]
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Ciências Agrárias e Veterinárias, Jaboticabalpt
unesp.departmentPatologia Veterinária - FCAVpt

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