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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/131427
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dc.contributor.authorAndré, Marcos Rogério-
dc.contributor.authorDumler, John Stephen-
dc.contributor.authorHerrera, Heitor M.-
dc.contributor.authorGonçalves, Luiz R.-
dc.contributor.authorSousa, Keyla C. M. de-
dc.contributor.authorScorpio, Diana Gerardi-
dc.contributor.authorSantis, Ana Cláudia Gabriela Alexandre de-
dc.contributor.authorDomingos, Iara Helena-
dc.contributor.authorMacedo, Gabriel Carvalho de-
dc.contributor.authorMachado, Rosangela Zacarias-
dc.date.accessioned2015-12-07T15:35:19Z-
dc.date.accessioned2016-10-25T21:23:30Z-
dc.date.available2015-12-07T15:35:19Z-
dc.date.available2016-10-25T21:23:30Z-
dc.date.issued2015-
dc.identifierhttp://dx.doi.org/10.1177/1098612X15593787-
dc.identifier.citationJournal Of Feline Medicine And Surgery, p. 1-9, 2015.-
dc.identifier.issn1532-2750-
dc.identifier.urihttp://hdl.handle.net/11449/131427-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/131427-
dc.description.abstractThe objective of this study was to develop a quantitative 5' nuclease real-time polymerase chain reaction (PCR) assay to diagnose infections caused by Bartonella species. Between January and April 2013 whole blood samples were collected by convenience from 151 cats (86 domiciled and 65 stray cats). The feline blood samples were subjected to a novel quantitative 5' nuclease real-time PCR (qPCR) for Bartonella species targeting the nictonamide adenine dinucleotide dehydrogenase gamma subunit (nuoG) and conventional PCR assays targeting intergenic transcribed spacer, ribC, gltA, pap31 and rpoB, followed by sequencing and basic local alignment search tool analysis. The qPCR assay detected as few as 10 copies of plasmid per reaction. Forty-six (54.4% domiciled and 45.6% stray cats) of 151 sampled cats showed positive results in nuoG qPCR for Bartonella species. The absolute quantification of nuoG Bartonella DNA in sampled cats ranged from 1.1 × 10(4) to 1.3 × 10(4). Eighteen (39.1%) of 46 positive samples in the qPCR were also positive in conventional PCR assays. The sequencing confirmed that Bartonella henselae and Bartonella clarridgeiae circulate in cats in midwestern Brazil. The present work provides details of a novel qPCR assay to diagnose infections caused by Bartonella species.en
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)-
dc.format.extent1-9-
dc.language.isoeng-
dc.publisherSAGE Publications-
dc.sourcePubMed-
dc.titleAssessment of a quantitative 5' nuclease real-time polymerase chain reaction using the nicotinamide adenine dinucleotide dehydrogenase gamma subunit (nuoG) for Bartonella species in domiciled and stray cats in Brazilen
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.contributor.institutionUniversity of Maryland-
dc.contributor.institutionJohns Hopkins School of Medicine-
dc.contributor.institutionDom Bosco Catholic University-
dc.contributor.institutionRoss University School of Veterinary Medicine-
dc.contributor.institutionZoonosis Control Center (CCZ)-
dc.description.affiliationPaulista State University (UNESP), Jaboticabal, São Paulo, Brazil-
dc.description.affiliationUniversity of Maryland, Baltimore, MD, USA Johns Hopkins School of Medicine, Baltimore, MD, USA.-
dc.description.affiliationDom Bosco Catholic University, Campo Grande, Mato Grosso do Sul, Brazil.-
dc.description.affiliationPaulista State University (UNESP), Jaboticabal, São Paulo, Brazil.-
dc.description.affiliationRoss University School of Veterinary Medicine, Basseterre, St Kitts, West Indies.-
dc.description.affiliationZoonosis Control Center (CCZ), Campo Grande, Mato Grosso do Sul, Brazil.-
dc.description.affiliationUnespPaulista State University (UNESP), Jaboticabal, São Paulo, Brazil-
dc.description.sponsorshipIdFAPESP: 2013/09889-0-
dc.identifier.doi10.1177/1098612X15593787-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofJournal Of Feline Medicine And Surgery-
dc.identifier.pubmed26138812-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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