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dc.contributor.author Fonseca, Tesiê Leopoldo
dc.contributor.author Moraes, Ernani Pinho de
dc.contributor.author Juliano, Carlos Renan Varela
dc.contributor.author Azambuja, Ana Maria Volkmer de
dc.contributor.author Scaini, Carlos James
dc.contributor.author Sassi, Raul Andrés Mendonza
dc.contributor.author Silva, Pedro Eduardo Almeida da
dc.date.accessioned 2015-06-03T14:33:24Z
dc.date.available 2015-06-03T14:33:24Z
dc.date.issued 2010
dc.identifier.citation FONSECA, Tesiê Leopoldo, et al. Detection of Helicobacter pylori by phenotypic and genotypic methods. Digestive Diseases and Sciences, v. 55, n. 6, p. 1643-1648, 2010. Disponível em: <http://link.springer.com/article/10.1007%2Fs10620-009-0928-8>. Acesso em: 22 maio 2015. pt_BR
dc.identifier.issn 0163-2116
dc.identifier.uri http://repositorio.furg.br/handle/1/4988
dc.description.abstract Aims This research evaluated the utilization of a urease in-house test, culture and molecular method (ureA PCR) as a diagnostic tool for Helicobacter pylori infection. Furthermore, we assessed the presence of the cagA gene in the specimens and in solated strains that were positive for ureA by PCR positive. Results Sensitivity and specificity, respectively, were 100 and 95.8% for the urease in-house test 93.3 and 95.8 for the ureA PCR assay of the specimen and 100 and 100% for the culture. The presence of the cagA gene was observed in eight (53%) ureA-positive samples. Conclusions In this study, we found that the PCR technique has applicability in the study of cagA, and other genes related to the H. pylori pathogen. This method can be applied to samples directly from biopsy or isolated from the bacteria. pt_BR
dc.language.iso eng pt_BR
dc.rights restrict access pt_BR
dc.subject H. pylori pt_BR
dc.subject Diagnostic pt_BR
dc.subject CagA pt_BR
dc.subject UreA pt_BR
dc.title Detection of Helicobacter pylori by phenotypic and genotypic methods pt_BR
dc.type article pt_BR
dc.identifier.doi 10.1007/s10620-009-0928-8 pt_BR


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