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Use este identificador para citar ou linkar para este item: https://repositorio.ufba.br/handle/ri/14844
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dc.contributor.authorNishi, Sandra Mayumi-
dc.contributor.authorSoares, Rodrigo Martins-
dc.contributor.authorDriemeier, David-
dc.contributor.authorAntoniassi, Nadia Aline Bobbi-
dc.contributor.authorSchares, Gereon-
dc.contributor.authorGennari, Solange Maria-
dc.contributor.authorAlves Neto, Aldo Francisco-
dc.creatorNishi, Sandra Mayumi-
dc.creatorSoares, Rodrigo Martins-
dc.creatorDriemeier, David-
dc.creatorAntoniassi, Nadia Aline Bobbi-
dc.creatorSchares, Gereon-
dc.creatorGennari, Solange Maria-
dc.creatorAlves Neto, Aldo Francisco-
dc.date.accessioned2014-04-22T18:37:29Z-
dc.date.available2014-04-22T18:37:29Z-
dc.date.issued2011-
dc.identifier.issn0022-3395-
dc.identifier.urihttp://repositorio.ufba.br/ri/handle/ri/14844-
dc.descriptionp. 135-139pt_BR
dc.description.abstractThe aim of the present study was to evaluate the viability of Neospora caninum sporulated oocysts after various chemical and physical treatments. Bioassays in gerbils and molecular techniques (PCR-RFLP) were used for identification of the oocysts shed by experimentally infected dogs. Sporulated oocysts were purified and divided into 11 treatment groups as follows: absolute ethanol for 1 hr; 20 C for 6 hr; 4 C for 6 hr; 60 C for 1 min; 100 C for 1 min; 10% formaldehyde for 1 hr; 10% ammonia for 1 hr; 2% iodine for 1 hr; 10% sodium hypochlorite for 1 hr; 70% ethanol for 1 hr; and one group was left untreated and kept as a positive control. All chemical treatments were performed at room temperature (37 C). A total of 33 gerbils, or 3 gerbils per treatment, were used for bioassays. After treatment, the oocysts were divided into aliquots of 1,000 oocysts and orally administered to gerbils. After 63 days, the gerbils were anesthetized and killed with 0.2 ml of T61; blood and tissue samples were collected for serological (IFAT and western blotting), molecular (real-time PCR), histopathology, and immunohistochemical tests. Treatments were considered effective only if all 5 detection techniques tested negative. High temperatures at 100 C for 1 min and 10% sodium hypochlorite for 1 hr were the only treatments that met this condition, effectively inactivating all oocysts.pt_BR
dc.language.isoenpt_BR
dc.rightsAcesso Abertopt_BR
dc.sourcehttp://dx.doi.org/ 10.1645/GE-2571.1pt_BR
dc.titleViability of Sporulated Oocysts of Neospora caninum After Exposure to Different Physical and Chemical Treatmentspt_BR
dc.title.alternativeJournal of Parasitologypt_BR
dc.typeArtigo de Periódicopt_BR
dc.identifier.numberv. 97, n. 1pt_BR
Aparece nas coleções:Artigo Publicado em Periódico (EMV)

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