Aldo-keto reductase and alcohol dehydrogenase contribute to benznidazole natural resistance in Trypanosoma cruzi

ABSTRACT: 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 paras...

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Autores:
González Uribe, Laura
García Huertas, Paola Alexandra
Triana Chávez, Omar
García, Gabriela Andrea
Fonseca Murta, Silvane María
Mejía Jaramillo, Ana María
Tipo de recurso:
Article of investigation
Fecha de publicación:
2017
Institución:
Universidad de Antioquia
Repositorio:
Repositorio UdeA
Idioma:
eng
OAI Identifier:
oai:bibliotecadigital.udea.edu.co:10495/20089
Acceso en línea:
http://hdl.handle.net/10495/20089
Palabra clave:
Enfermedad de Chagas
Chagas Disease
Trypanosoma cruzi
Resistencia a múltiples medicamentos
Drug Resistance, Multiple
Benznidazoles
Rights
openAccess
License
http://creativecommons.org/licenses/by/2.5/co/
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oai_identifier_str oai:bibliotecadigital.udea.edu.co:10495/20089
network_acronym_str UDEA2
network_name_str Repositorio UdeA
repository_id_str
dc.title.spa.fl_str_mv Aldo-keto reductase and alcohol dehydrogenase contribute to benznidazole natural resistance in Trypanosoma cruzi
title Aldo-keto reductase and alcohol dehydrogenase contribute to benznidazole natural resistance in Trypanosoma cruzi
spellingShingle Aldo-keto reductase and alcohol dehydrogenase contribute to benznidazole natural resistance in Trypanosoma cruzi
Enfermedad de Chagas
Chagas Disease
Trypanosoma cruzi
Resistencia a múltiples medicamentos
Drug Resistance, Multiple
Benznidazoles
title_short Aldo-keto reductase and alcohol dehydrogenase contribute to benznidazole natural resistance in Trypanosoma cruzi
title_full Aldo-keto reductase and alcohol dehydrogenase contribute to benznidazole natural resistance in Trypanosoma cruzi
title_fullStr Aldo-keto reductase and alcohol dehydrogenase contribute to benznidazole natural resistance in Trypanosoma cruzi
title_full_unstemmed Aldo-keto reductase and alcohol dehydrogenase contribute to benznidazole natural resistance in Trypanosoma cruzi
title_sort Aldo-keto reductase and alcohol dehydrogenase contribute to benznidazole natural resistance in Trypanosoma cruzi
dc.creator.fl_str_mv González Uribe, Laura
García Huertas, Paola Alexandra
Triana Chávez, Omar
García, Gabriela Andrea
Fonseca Murta, Silvane María
Mejía Jaramillo, Ana María
dc.contributor.author.none.fl_str_mv González Uribe, Laura
García Huertas, Paola Alexandra
Triana Chávez, Omar
García, Gabriela Andrea
Fonseca Murta, Silvane María
Mejía Jaramillo, Ana María
dc.contributor.researchgroup.spa.fl_str_mv Biología y Control de Enfermedades Infecciosas
dc.subject.decs.none.fl_str_mv Enfermedad de Chagas
Chagas Disease
Trypanosoma cruzi
Resistencia a múltiples medicamentos
Drug Resistance, Multiple
topic Enfermedad de Chagas
Chagas Disease
Trypanosoma cruzi
Resistencia a múltiples medicamentos
Drug Resistance, Multiple
Benznidazoles
dc.subject.proposal.spa.fl_str_mv Benznidazoles
description ABSTRACT: 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.
publishDate 2017
dc.date.issued.none.fl_str_mv 2017
dc.date.accessioned.none.fl_str_mv 2021-06-11T03:14:33Z
dc.date.available.none.fl_str_mv 2021-06-11T03:14:33Z
dc.type.spa.fl_str_mv Artículo de investigación
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dc.identifier.issn.none.fl_str_mv 0950-382X
dc.identifier.uri.none.fl_str_mv http://hdl.handle.net/10495/20089
dc.identifier.doi.none.fl_str_mv 10.1111/mmi.13830
dc.identifier.eissn.none.fl_str_mv 1365-2958
identifier_str_mv 0950-382X
10.1111/mmi.13830
1365-2958
url http://hdl.handle.net/10495/20089
dc.language.iso.spa.fl_str_mv eng
language eng
dc.relation.ispartofjournalabbrev.spa.fl_str_mv Mol. microbiol.
dc.relation.citationendpage.spa.fl_str_mv 718
dc.relation.citationissue.spa.fl_str_mv 5
dc.relation.citationstartpage.spa.fl_str_mv 704
dc.relation.citationvolume.spa.fl_str_mv 106
dc.relation.ispartofjournal.spa.fl_str_mv Molecular microbiology
dc.rights.uri.*.fl_str_mv http://creativecommons.org/licenses/by/2.5/co/
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dc.format.extent.spa.fl_str_mv 15
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dc.publisher.spa.fl_str_mv Blackwell Scientific Publications
dc.publisher.place.spa.fl_str_mv Oxford, Inglaterra
institution Universidad de Antioquia
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spelling González Uribe, LauraGarcía Huertas, Paola AlexandraTriana Chávez, OmarGarcía, Gabriela AndreaFonseca Murta, Silvane MaríaMejía Jaramillo, Ana MaríaBiología y Control de Enfermedades Infecciosas2021-06-11T03:14:33Z2021-06-11T03:14:33Z20170950-382Xhttp://hdl.handle.net/10495/2008910.1111/mmi.138301365-2958ABSTRACT: 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.COL000786515application/pdfengBlackwell Scientific PublicationsOxford, Inglaterrahttp://creativecommons.org/licenses/by/2.5/co/https://creativecommons.org/licenses/by/4.0/info:eu-repo/semantics/openAccesshttp://purl.org/coar/access_right/c_abf2Aldo-keto reductase and alcohol dehydrogenase contribute to benznidazole natural resistance in Trypanosoma cruziArtículo de investigaciónhttp://purl.org/coar/resource_type/c_2df8fbb1https://purl.org/redcol/resource_type/ARThttp://purl.org/coar/version/c_970fb48d4fbd8a85info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionEnfermedad de ChagasChagas DiseaseTrypanosoma cruziResistencia a múltiples medicamentosDrug Resistance, MultipleBenznidazolesMol. microbiol.7185704106Molecular microbiologyPublicationCC-LICENSElicense_rdflicense_rdfapplication/rdf+xml; charset=utf-8927https://bibliotecadigital.udea.edu.co/bitstreams/23f17cd6-f666-4eb5-905e-cd8a420aab28/download1646d1f6b96dbbbc38035efc9239ac9cMD52falseAnonymousREADLICENSElicense.txtlicense.txttext/plain; charset=utf-81748https://bibliotecadigital.udea.edu.co/bitstreams/8edbfe6d-229f-4aed-9882-6692bfdce0dd/download8a4605be74aa9ea9d79846c1fba20a33MD53falseAnonymousREADORIGINALGonzálezLaura_2017_Aldo-KetoResistanceTrypanosoma.pdfGonzálezLaura_2017_Aldo-KetoResistanceTrypanosoma.pdfArtículo de investigaciónapplication/pdf787542https://bibliotecadigital.udea.edu.co/bitstreams/5ba88054-7dd5-4c0b-87cb-c6b0bc4d887b/downloadf0ccfcae6538d04d1ba4473abe8d5469MD51trueAnonymousREADTEXTGonzálezLaura_2017_Aldo-KetoResistanceTrypanosoma.pdf.txtGonzálezLaura_2017_Aldo-KetoResistanceTrypanosoma.pdf.txtExtracted texttext/plain74760https://bibliotecadigital.udea.edu.co/bitstreams/593f40f2-f747-4249-a348-8049c522cc5e/download97389fa873c8784edb6fecfd8ae088a6MD54falseAnonymousREADTHUMBNAILGonzálezLaura_2017_Aldo-KetoResistanceTrypanosoma.pdf.jpgGonzálezLaura_2017_Aldo-KetoResistanceTrypanosoma.pdf.jpgGenerated Thumbnailimage/jpeg16925https://bibliotecadigital.udea.edu.co/bitstreams/6a17f933-3c80-416f-b926-4212597c9ca9/download8e927e0758211dddb113dbed19f04916MD55falseAnonymousREAD10495/20089oai:bibliotecadigital.udea.edu.co:10495/200892025-03-27 01:00:17.163http://creativecommons.org/licenses/by/2.5/co/open.accesshttps://bibliotecadigital.udea.edu.coRepositorio Institucional de la Universidad de Antioquiaaplicacionbibliotecadigitalbiblioteca@udea.edu.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