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dc.contributor.authorGonzález Uribe, Laura-
dc.contributor.authorGarcía Huertas, Paola Alexandra-
dc.contributor.authorTriana Chávez, Omar-
dc.contributor.authorGarcía, Gabriela Andrea-
dc.contributor.authorFonseca Murta, Silvane María-
dc.contributor.authorMejía Jaramillo, Ana María-
dc.date.accessioned2021-06-11T03:14:33Z-
dc.date.available2021-06-11T03:14:33Z-
dc.date.issued2017-
dc.identifier.issn0950-382X-
dc.identifier.urihttp://hdl.handle.net/10495/20089-
dc.description.abstractABSTRACT: The improvement of Chagas disease treatment is focused not only on the development of new drugs but also in understanding mechanisms of action and resistance to drugs conventionally used. Thus, some strategies aim to detect specific changes in proteins between sensitive and resistant parasites and to evaluate the role played in these processes by functional genomics. In this work, we used a natural Trypanosoma cruzi population resistant to benznidazole, which has clones with different susceptibilities to this drug without alterations in the NTR I gene. Using 2DE-gel electrophoresis, the aldo-keto reductase and the alcohol dehydrogenase proteins were found up regulated in the natural resistant clone and therefore their possible role in the resistance to benznidazoleand glyoxal was investigated. Both genes were overexpressed in a drug sensitive T. cruzi clone and the biological changes in response to these compounds were evaluated. The results showed that the overexpression of these proteins enhances resistance to benznidazole and glyoxal in T. cruzi. Moreover, a decrease in mitochondrial and cell membrane damage was observed, accompanied by a drop in the intracellular concentration of reactive oxygen species after treatment. Our results suggest that these proteins are involved in the mechanism of action of benznidazole.spa
dc.format.extent15spa
dc.format.mimetypeapplication/pdfspa
dc.language.isoengspa
dc.publisherBlackwell Scientific Publicationsspa
dc.type.hasversioninfo:eu-repo/semantics/publishedVersionspa
dc.rightsinfo:eu-repo/semantics/openAccessspa
dc.rights.urihttp://creativecommons.org/licenses/by/2.5/co/*
dc.titleAldo-keto reductase and alcohol dehydrogenase contribute to benznidazole natural resistance in Trypanosoma cruzispa
dc.typeinfo:eu-repo/semantics/articlespa
dc.publisher.groupBiología y Control de Enfermedades Infecciosasspa
dc.identifier.doi10.1111/mmi.13830-
oaire.versionhttp://purl.org/coar/version/c_970fb48d4fbd8a85spa
dc.rights.accessrightshttp://purl.org/coar/access_right/c_abf2spa
dc.identifier.eissn1365-2958-
oaire.citationtitleMolecular microbiologyspa
oaire.citationstartpage704spa
oaire.citationendpage718spa
oaire.citationvolume106spa
oaire.citationissue5spa
dc.rights.creativecommonshttps://creativecommons.org/licenses/by/4.0/spa
dc.publisher.placeOxford, Inglaterraspa
dc.type.coarhttp://purl.org/coar/resource_type/c_2df8fbb1spa
dc.type.redcolhttps://purl.org/redcol/resource_type/ARTspa
dc.type.localArtículo de investigaciónspa
dc.subject.decsEnfermedad de Chagas-
dc.subject.decsChagas Disease-
dc.subject.decsTrypanosoma cruzi-
dc.subject.decsResistencia a múltiples medicamentos-
dc.subject.decsDrug Resistance, Multiple-
dc.subject.proposalBenznidazolesspa
dc.description.researchgroupidCOL0007865spa
dc.relation.ispartofjournalabbrevMol. microbiol.spa
Aparece en las colecciones: Artículos de Revista en Ciencias Exactas y Naturales

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