Identification of a field isolate of Fasciola hepatica resistant to albendazole and susceptible to triclabendazole
- Autores
- Sanabria, Rodrigo Eduardo Fabrizio; Ceballos, Laura; Moreno, Laura; Romero, Jorge Marcelo; Lanusse Carlos; Alvarez, Luis Ignacio
- Año de publicación
- 2013
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- The experiments described here were designed to characterize the status of susceptibility/resistance to albendazole (ABZ) and triclabendazole (TCBZ) of a Fasciola hepatica isolate (named CEDIVE isolate) recovered from infected sheep (Gualeguay, Argentina) and maintained under laboratory conditions. Two separate clinical efficacy experiments were performed on sheep artificially infected with the CEDIVE isolate. Experiment 1: Sheep were randomly distributed either in an untreated control group or an ABZ (7.5 mg/kg) treated group (n= 4 each). Additionally, the systemic exposure of ABZ metabolites was assessed in those ABZ-treated infected animals. In Experiment 2, an untreated control group and a TCBZ (10 mg/kg) treated group was included (n = 4 each). The fluckicidal efficacy of ABZ and TCBZ was assessed by comparison of the number of flukes recovered from untreated and treated sheep at 15 days post-treatment. The efficacy against the CEDIVE isolate of F. hepatica was 29% (ABZ) and 100% (TCBZ). The plasma drug exposure (expressed as AUC and Cmax) observed in the ABZ treated animals (Experiment 1), was in agreement with data obtained in previous studies, which indicate that the low ABZ efficacy was not related to the quality of the pharmaceutical product and/or to a low systemic availability of the active drug/metabolite. The results reported here, clearly show that the CEDIVE isolate of F. hepatica behaves as resistant to ABZ and susceptible to TCBZ.
Fil: Sanabria, Rodrigo Eduardo Fabrizio. Universidad Nacional de la Plata. Facultad de Ciencias Veterinarias; Argentina
Fil: Ceballos, Laura. Universidad Nacional del Centro de la Provincia de Buenos Aires.. Facultad de Ciencias Veterinarias. Departamento de Fisiopatologia. Laboratorio de Farmacologia; Argentina
Fil: Moreno, Laura. Universidad Nacional del Centro de la Provincia de Buenos Aires.. Facultad de Ciencias Veterinarias. Departamento de Fisiopatologia. Laboratorio de Farmacologia; Argentina
Fil: Romero, Jorge Marcelo. Universidad Nacional de la Plata. Facultad de Ciencias Veterinarias; Argentina
Fil: Lanusse Carlos. Universidad Nacional del Centro de la Provincia de Buenos Aires.. Facultad de Ciencias Veterinarias. Departamento de Fisiopatologia. Laboratorio de Farmacologia; Argentina
Fil: Alvarez, Luis Ignacio. Universidad Nacional del Centro de la Provincia de Buenos Aires.. Facultad de Ciencias Veterinarias. Departamento de Fisiopatologia. Laboratorio de Farmacologia; Argentina - Materia
-
Fasciola Hepatica Isolate
Resistance
Albendazole
Triclabendazole - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
- Repositorio
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/992
Ver los metadatos del registro completo
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oai:ri.conicet.gov.ar:11336/992 |
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Identification of a field isolate of Fasciola hepatica resistant to albendazole and susceptible to triclabendazoleSanabria, Rodrigo Eduardo FabrizioCeballos, LauraMoreno, LauraRomero, Jorge MarceloLanusse CarlosAlvarez, Luis IgnacioFasciola Hepatica IsolateResistanceAlbendazoleTriclabendazolehttps://purl.org/becyt/ford/4.3https://purl.org/becyt/ford/4The experiments described here were designed to characterize the status of susceptibility/resistance to albendazole (ABZ) and triclabendazole (TCBZ) of a Fasciola hepatica isolate (named CEDIVE isolate) recovered from infected sheep (Gualeguay, Argentina) and maintained under laboratory conditions. Two separate clinical efficacy experiments were performed on sheep artificially infected with the CEDIVE isolate. Experiment 1: Sheep were randomly distributed either in an untreated control group or an ABZ (7.5 mg/kg) treated group (n= 4 each). Additionally, the systemic exposure of ABZ metabolites was assessed in those ABZ-treated infected animals. In Experiment 2, an untreated control group and a TCBZ (10 mg/kg) treated group was included (n = 4 each). The fluckicidal efficacy of ABZ and TCBZ was assessed by comparison of the number of flukes recovered from untreated and treated sheep at 15 days post-treatment. The efficacy against the CEDIVE isolate of F. hepatica was 29% (ABZ) and 100% (TCBZ). The plasma drug exposure (expressed as AUC and Cmax) observed in the ABZ treated animals (Experiment 1), was in agreement with data obtained in previous studies, which indicate that the low ABZ efficacy was not related to the quality of the pharmaceutical product and/or to a low systemic availability of the active drug/metabolite. The results reported here, clearly show that the CEDIVE isolate of F. hepatica behaves as resistant to ABZ and susceptible to TCBZ.Fil: Sanabria, Rodrigo Eduardo Fabrizio. Universidad Nacional de la Plata. Facultad de Ciencias Veterinarias; ArgentinaFil: Ceballos, Laura. Universidad Nacional del Centro de la Provincia de Buenos Aires.. Facultad de Ciencias Veterinarias. Departamento de Fisiopatologia. Laboratorio de Farmacologia; ArgentinaFil: Moreno, Laura. Universidad Nacional del Centro de la Provincia de Buenos Aires.. Facultad de Ciencias Veterinarias. Departamento de Fisiopatologia. Laboratorio de Farmacologia; ArgentinaFil: Romero, Jorge Marcelo. Universidad Nacional de la Plata. Facultad de Ciencias Veterinarias; ArgentinaFil: Lanusse Carlos. Universidad Nacional del Centro de la Provincia de Buenos Aires.. Facultad de Ciencias Veterinarias. Departamento de Fisiopatologia. Laboratorio de Farmacologia; ArgentinaFil: Alvarez, Luis Ignacio. Universidad Nacional del Centro de la Provincia de Buenos Aires.. Facultad de Ciencias Veterinarias. Departamento de Fisiopatologia. Laboratorio de Farmacologia; ArgentinaElsevier Science Bv2013-05info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/992Sanabria, Rodrigo Eduardo Fabrizio; Ceballos, Laura; Moreno, Laura; Romero, Jorge Marcelo; Lanusse Carlos; et al.; Identification of a field isolate of Fasciola hepatica resistant to albendazole and susceptible to triclabendazole; Elsevier Science Bv; Veterinary Parasitology; 193; 5-2013; 105-1100304-4017enginfo:eu-repo/semantics/altIdentifier/url/http://www.ncbi.nlm.nih.gov/pubmed/23273779info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-03T10:09:50Zoai:ri.conicet.gov.ar:11336/992instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-09-03 10:09:50.446CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
dc.title.none.fl_str_mv |
Identification of a field isolate of Fasciola hepatica resistant to albendazole and susceptible to triclabendazole |
title |
Identification of a field isolate of Fasciola hepatica resistant to albendazole and susceptible to triclabendazole |
spellingShingle |
Identification of a field isolate of Fasciola hepatica resistant to albendazole and susceptible to triclabendazole Sanabria, Rodrigo Eduardo Fabrizio Fasciola Hepatica Isolate Resistance Albendazole Triclabendazole |
title_short |
Identification of a field isolate of Fasciola hepatica resistant to albendazole and susceptible to triclabendazole |
title_full |
Identification of a field isolate of Fasciola hepatica resistant to albendazole and susceptible to triclabendazole |
title_fullStr |
Identification of a field isolate of Fasciola hepatica resistant to albendazole and susceptible to triclabendazole |
title_full_unstemmed |
Identification of a field isolate of Fasciola hepatica resistant to albendazole and susceptible to triclabendazole |
title_sort |
Identification of a field isolate of Fasciola hepatica resistant to albendazole and susceptible to triclabendazole |
dc.creator.none.fl_str_mv |
Sanabria, Rodrigo Eduardo Fabrizio Ceballos, Laura Moreno, Laura Romero, Jorge Marcelo Lanusse Carlos Alvarez, Luis Ignacio |
author |
Sanabria, Rodrigo Eduardo Fabrizio |
author_facet |
Sanabria, Rodrigo Eduardo Fabrizio Ceballos, Laura Moreno, Laura Romero, Jorge Marcelo Lanusse Carlos Alvarez, Luis Ignacio |
author_role |
author |
author2 |
Ceballos, Laura Moreno, Laura Romero, Jorge Marcelo Lanusse Carlos Alvarez, Luis Ignacio |
author2_role |
author author author author author |
dc.subject.none.fl_str_mv |
Fasciola Hepatica Isolate Resistance Albendazole Triclabendazole |
topic |
Fasciola Hepatica Isolate Resistance Albendazole Triclabendazole |
purl_subject.fl_str_mv |
https://purl.org/becyt/ford/4.3 https://purl.org/becyt/ford/4 |
dc.description.none.fl_txt_mv |
The experiments described here were designed to characterize the status of susceptibility/resistance to albendazole (ABZ) and triclabendazole (TCBZ) of a Fasciola hepatica isolate (named CEDIVE isolate) recovered from infected sheep (Gualeguay, Argentina) and maintained under laboratory conditions. Two separate clinical efficacy experiments were performed on sheep artificially infected with the CEDIVE isolate. Experiment 1: Sheep were randomly distributed either in an untreated control group or an ABZ (7.5 mg/kg) treated group (n= 4 each). Additionally, the systemic exposure of ABZ metabolites was assessed in those ABZ-treated infected animals. In Experiment 2, an untreated control group and a TCBZ (10 mg/kg) treated group was included (n = 4 each). The fluckicidal efficacy of ABZ and TCBZ was assessed by comparison of the number of flukes recovered from untreated and treated sheep at 15 days post-treatment. The efficacy against the CEDIVE isolate of F. hepatica was 29% (ABZ) and 100% (TCBZ). The plasma drug exposure (expressed as AUC and Cmax) observed in the ABZ treated animals (Experiment 1), was in agreement with data obtained in previous studies, which indicate that the low ABZ efficacy was not related to the quality of the pharmaceutical product and/or to a low systemic availability of the active drug/metabolite. The results reported here, clearly show that the CEDIVE isolate of F. hepatica behaves as resistant to ABZ and susceptible to TCBZ. Fil: Sanabria, Rodrigo Eduardo Fabrizio. Universidad Nacional de la Plata. Facultad de Ciencias Veterinarias; Argentina Fil: Ceballos, Laura. Universidad Nacional del Centro de la Provincia de Buenos Aires.. Facultad de Ciencias Veterinarias. Departamento de Fisiopatologia. Laboratorio de Farmacologia; Argentina Fil: Moreno, Laura. Universidad Nacional del Centro de la Provincia de Buenos Aires.. Facultad de Ciencias Veterinarias. Departamento de Fisiopatologia. Laboratorio de Farmacologia; Argentina Fil: Romero, Jorge Marcelo. Universidad Nacional de la Plata. Facultad de Ciencias Veterinarias; Argentina Fil: Lanusse Carlos. Universidad Nacional del Centro de la Provincia de Buenos Aires.. Facultad de Ciencias Veterinarias. Departamento de Fisiopatologia. Laboratorio de Farmacologia; Argentina Fil: Alvarez, Luis Ignacio. Universidad Nacional del Centro de la Provincia de Buenos Aires.. Facultad de Ciencias Veterinarias. Departamento de Fisiopatologia. Laboratorio de Farmacologia; Argentina |
description |
The experiments described here were designed to characterize the status of susceptibility/resistance to albendazole (ABZ) and triclabendazole (TCBZ) of a Fasciola hepatica isolate (named CEDIVE isolate) recovered from infected sheep (Gualeguay, Argentina) and maintained under laboratory conditions. Two separate clinical efficacy experiments were performed on sheep artificially infected with the CEDIVE isolate. Experiment 1: Sheep were randomly distributed either in an untreated control group or an ABZ (7.5 mg/kg) treated group (n= 4 each). Additionally, the systemic exposure of ABZ metabolites was assessed in those ABZ-treated infected animals. In Experiment 2, an untreated control group and a TCBZ (10 mg/kg) treated group was included (n = 4 each). The fluckicidal efficacy of ABZ and TCBZ was assessed by comparison of the number of flukes recovered from untreated and treated sheep at 15 days post-treatment. The efficacy against the CEDIVE isolate of F. hepatica was 29% (ABZ) and 100% (TCBZ). The plasma drug exposure (expressed as AUC and Cmax) observed in the ABZ treated animals (Experiment 1), was in agreement with data obtained in previous studies, which indicate that the low ABZ efficacy was not related to the quality of the pharmaceutical product and/or to a low systemic availability of the active drug/metabolite. The results reported here, clearly show that the CEDIVE isolate of F. hepatica behaves as resistant to ABZ and susceptible to TCBZ. |
publishDate |
2013 |
dc.date.none.fl_str_mv |
2013-05 |
dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion http://purl.org/coar/resource_type/c_6501 info:ar-repo/semantics/articulo |
format |
article |
status_str |
publishedVersion |
dc.identifier.none.fl_str_mv |
http://hdl.handle.net/11336/992 Sanabria, Rodrigo Eduardo Fabrizio; Ceballos, Laura; Moreno, Laura; Romero, Jorge Marcelo; Lanusse Carlos; et al.; Identification of a field isolate of Fasciola hepatica resistant to albendazole and susceptible to triclabendazole; Elsevier Science Bv; Veterinary Parasitology; 193; 5-2013; 105-110 0304-4017 |
url |
http://hdl.handle.net/11336/992 |
identifier_str_mv |
Sanabria, Rodrigo Eduardo Fabrizio; Ceballos, Laura; Moreno, Laura; Romero, Jorge Marcelo; Lanusse Carlos; et al.; Identification of a field isolate of Fasciola hepatica resistant to albendazole and susceptible to triclabendazole; Elsevier Science Bv; Veterinary Parasitology; 193; 5-2013; 105-110 0304-4017 |
dc.language.none.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
info:eu-repo/semantics/altIdentifier/url/http://www.ncbi.nlm.nih.gov/pubmed/23273779 |
dc.rights.none.fl_str_mv |
info:eu-repo/semantics/openAccess https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
eu_rights_str_mv |
openAccess |
rights_invalid_str_mv |
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
dc.format.none.fl_str_mv |
application/pdf application/pdf application/pdf |
dc.publisher.none.fl_str_mv |
Elsevier Science Bv |
publisher.none.fl_str_mv |
Elsevier Science Bv |
dc.source.none.fl_str_mv |
reponame:CONICET Digital (CONICET) instname:Consejo Nacional de Investigaciones Científicas y Técnicas |
reponame_str |
CONICET Digital (CONICET) |
collection |
CONICET Digital (CONICET) |
instname_str |
Consejo Nacional de Investigaciones Científicas y Técnicas |
repository.name.fl_str_mv |
CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas |
repository.mail.fl_str_mv |
dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar |
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13.13397 |