dc.creatorNaidich, Ariel
dc.creatorMcManus, Donald P
dc.creatorCanova, S G
dc.creatorGutierrez, Ariana M.
dc.creatorZhang, Wenbao
dc.creatorGuarnera, Eduardo
dc.creatorRosenzvit, Mara Cecilia
dc.date2021-01-22T19:25:25Z
dc.date2021-01-22T19:25:25Z
dc.date2006-02
dc.date.accessioned2023-08-29T20:09:04Z
dc.date.available2023-08-29T20:09:04Z
dc.identifier0890-8508
dc.identifierhttp://sgc.anlis.gob.ar/handle/123456789/2225
dc.identifier10.1016/j.mcp.2005.08.001
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/8520486
dc.descriptionFil: Naidich, Ariel. ANLIS Dr.C.G.Malbrán. Instituto Nacional de Enfermedades Infecciosas. Departamento de Parasitología; Argentina.
dc.descriptionFil: McManus, Donald P. Royal Brisbane Hospital Post Office. Queensland Institute of Medical Research. Molecular Parasitology Laboratory. Division of Infectious Diseases and Immunology; Australia.
dc.descriptionFil: Canova, Sergio G. ANLIS Dr.C.G.Malbrán. Instituto Nacional de Enfermedades Infecciosas. Departamento de Parasitología; Argentina.
dc.descriptionFil: Gutierrez, Ariana M. ANLIS Dr.C.G.Malbrán. Instituto Nacional de Enfermedades Infecciosas. Departamento de Parasitología; Argentina.
dc.descriptionFil: Zhang, Wenbao. Royal Brisbane Hospital Post Office. Queensland Institute of Medical Research. Molecular Parasitology Laboratory. Division of Infectious Diseases and Immunology; Australia.
dc.descriptionFil: Guarnera, Eduardo A. ANLIS Dr.C.G.Malbrán. Instituto Nacional de Enfermedades Infecciosas. Departamento de Parasitología; Argentina.
dc.descriptionFil: Rosenzvit, Mara Cecilia. ANLIS Dr.C.G.Malbrán. Instituto Nacional de Enfermedades Infecciosas. Departamento de Parasitología; Argentina.
dc.descriptionThe detection of Echinococcus granulosus in dogs is important for epidemiological surveillance and evaluation of cystic hydatic disease control programs. We report the efficacy of two PCR-based methods to detect patent and pre-patent infection in dogs experimentally infected with E. granulosus. The detection is based on amplification of a fragment of a mitochondrial gene (Mit-PCR) and a DNA repetitive element (Rep-PCR) of E. granulosus. We tested the ability of both methods to detect several genotypes of the parasite. Both PCR methods could detect E. granulosus in pre-patent and patent periods, even when microscopical observation of eggs resulted negative in fecal samples. The Mit-PCR produced the same amplification pattern for all the parasite genotypes tested while the amplification patterns with the Rep-PCR differed among groups of strains. Fecal samples collected from dogs of an endemic area were diagnosed with more sensitivity than arecoline hydrobromide purgation. These molecular methods could be applied in the confirmation of coproantigen-positive fecal samples and to verify the success of control programs.
dc.formatpdf
dc.languageen
dc.relationMolecular and cellular probes
dc.rightsnone
dc.sourceMolecular and Cellular Probes 2006;20(1):5-10
dc.subjectEchinococcus granulosus
dc.subjectEquinococosis
dc.subjectPatente
dc.titlePatent and pre-patent detection of Echinococcus granulosus genotypes in the definitive host
dc.typeArtículo


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