dc.contributorUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2015-12-07T15:39:55Z
dc.date.available2015-12-07T15:39:55Z
dc.date.created2015-12-07T15:39:55Z
dc.date.issued2015-10-28
dc.identifierJournal Of Microbiological Methods, p. 1-25, 2015.
dc.identifier1872-8359
dc.identifierhttp://hdl.handle.net/11449/131669
dc.identifier10.1016/j.mimet.2015.10.021
dc.identifier26519771
dc.description.abstractStreptococcus agalactiae (GBS) are Gram-positive cocci responsible for substantial losses in tilapia fish farms in Brazil and worldwide. It causes septicemia, meningoencephalitis and mortality of whole shoals that can occur within 72h. Thus, diagnostic methods are needed that are rapid, specific and sensitive. In this study, a pair of specific primers for GBS was generated based on the cfb gene sequence and initially evaluated by conventional PCR. The protocols for absolute quantitative real-time PCR (qPCR) were then adapted to validate the technique for the identification and quantification of GBS isolated by real-time detection of amplicons using fluorescence measurements. Finally, an infectivity test was conducted in tilapia infected with GBS strains. Total DNA from the host brain was subjected to the same technique, and the strains were re-isolated to validate Koch's postulates. The assay showed 100% specificity for the other bacterial species evaluated and a sensitivity of 367 gene copies per 20mg of brain tissue within 4h, making this test a valuable tool for health monitoring programs.
dc.languageeng
dc.publisherElsevier B. V.
dc.relationJournal Of Microbiological Methods
dc.rightsAcesso restrito
dc.sourcePubMed
dc.subjectBrazil
dc.subjectCamp factor
dc.subjectStreptococcosis
dc.subjectTilapia
dc.titleValidation of absolute quantitative real-time PCR for the diagnosis of streptococcus agalactiae in fish
dc.typeArtículos de revistas


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