A Multiplatform Metabolomic Approach to the Basis of Antimonial Action and Resistance in Leishmania infantum.

There is a rising resistance against antimony drugs, the gold-standard for treatment until some years ago. That is a serious problem due to the paucity of drugs in current clinical use. In a research to reveal how these drugs affect the parasite during treatment and to unravel the underlying basis f...

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Main Authors: David Rojo, Gisele A B Canuto, Emerson A Castilho-Martins, Marina F M Tavares, Coral Barbas, Ángeles López-Gonzálvez, Luis Rivas
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2015-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC4498920?pdf=render
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spelling doaj-8478b959aac14d22980b55d7bba96bf62020-11-25T01:21:27ZengPublic Library of Science (PLoS)PLoS ONE1932-62032015-01-01107e013067510.1371/journal.pone.0130675A Multiplatform Metabolomic Approach to the Basis of Antimonial Action and Resistance in Leishmania infantum.David RojoGisele A B CanutoEmerson A Castilho-MartinsMarina F M TavaresCoral BarbasÁngeles López-GonzálvezLuis RivasThere is a rising resistance against antimony drugs, the gold-standard for treatment until some years ago. That is a serious problem due to the paucity of drugs in current clinical use. In a research to reveal how these drugs affect the parasite during treatment and to unravel the underlying basis for their resistance, we have employed metabolomics to study treatment in Leishmania infantum promastigotes. This was accomplished first through the untargeted analysis of metabolic snapshots of treated and untreated parasites both resistant and responders, utilizing a multiplatform approach to give the widest as possible coverage of the metabolome, and additionally through novel monitoring of the origin of the detected alterations through a 13C traceability experiment. Our data stress a multi-target metabolic alteration with treatment, affecting in particular the cell redox system that is essential to cope with detoxification and biosynthetic processes. Additionally, relevant changes were noted in amino acid metabolism. Our results are in agreement with other authors studying other Leishmania species.http://europepmc.org/articles/PMC4498920?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author David Rojo
Gisele A B Canuto
Emerson A Castilho-Martins
Marina F M Tavares
Coral Barbas
Ángeles López-Gonzálvez
Luis Rivas
spellingShingle David Rojo
Gisele A B Canuto
Emerson A Castilho-Martins
Marina F M Tavares
Coral Barbas
Ángeles López-Gonzálvez
Luis Rivas
A Multiplatform Metabolomic Approach to the Basis of Antimonial Action and Resistance in Leishmania infantum.
PLoS ONE
author_facet David Rojo
Gisele A B Canuto
Emerson A Castilho-Martins
Marina F M Tavares
Coral Barbas
Ángeles López-Gonzálvez
Luis Rivas
author_sort David Rojo
title A Multiplatform Metabolomic Approach to the Basis of Antimonial Action and Resistance in Leishmania infantum.
title_short A Multiplatform Metabolomic Approach to the Basis of Antimonial Action and Resistance in Leishmania infantum.
title_full A Multiplatform Metabolomic Approach to the Basis of Antimonial Action and Resistance in Leishmania infantum.
title_fullStr A Multiplatform Metabolomic Approach to the Basis of Antimonial Action and Resistance in Leishmania infantum.
title_full_unstemmed A Multiplatform Metabolomic Approach to the Basis of Antimonial Action and Resistance in Leishmania infantum.
title_sort multiplatform metabolomic approach to the basis of antimonial action and resistance in leishmania infantum.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2015-01-01
description There is a rising resistance against antimony drugs, the gold-standard for treatment until some years ago. That is a serious problem due to the paucity of drugs in current clinical use. In a research to reveal how these drugs affect the parasite during treatment and to unravel the underlying basis for their resistance, we have employed metabolomics to study treatment in Leishmania infantum promastigotes. This was accomplished first through the untargeted analysis of metabolic snapshots of treated and untreated parasites both resistant and responders, utilizing a multiplatform approach to give the widest as possible coverage of the metabolome, and additionally through novel monitoring of the origin of the detected alterations through a 13C traceability experiment. Our data stress a multi-target metabolic alteration with treatment, affecting in particular the cell redox system that is essential to cope with detoxification and biosynthetic processes. Additionally, relevant changes were noted in amino acid metabolism. Our results are in agreement with other authors studying other Leishmania species.
url http://europepmc.org/articles/PMC4498920?pdf=render
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