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Drug resistance analysis by next generation sequencing in Leishmania

The use of next generation sequencing has the power to expedite the identification of drug resistance determinants and biomarkers and was applied successfully to drug resistance studies in Leishmania. This allowed the identification of modulation in gene expression, gene dosage alterations, changes...

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Autores principales: Leprohon, Philippe, Fernandez-Prada, Christopher, Gazanion, Élodie, Monte-Neto, Rubens, Ouellette, Marc
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4412915/
https://www.ncbi.nlm.nih.gov/pubmed/25941624
http://dx.doi.org/10.1016/j.ijpddr.2014.09.005
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author Leprohon, Philippe
Fernandez-Prada, Christopher
Gazanion, Élodie
Monte-Neto, Rubens
Ouellette, Marc
author_facet Leprohon, Philippe
Fernandez-Prada, Christopher
Gazanion, Élodie
Monte-Neto, Rubens
Ouellette, Marc
author_sort Leprohon, Philippe
collection PubMed
description The use of next generation sequencing has the power to expedite the identification of drug resistance determinants and biomarkers and was applied successfully to drug resistance studies in Leishmania. This allowed the identification of modulation in gene expression, gene dosage alterations, changes in chromosome copy numbers and single nucleotide polymorphisms that correlated with resistance in Leishmania strains derived from the laboratory and from the field. An impressive heterogeneity at the population level was also observed, individual clones within populations often differing in both genotypes and phenotypes, hence complicating the elucidation of resistance mechanisms. This review summarizes the most recent highlights that whole genome sequencing brought to our understanding of Leishmania drug resistance and likely new directions.
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spelling pubmed-44129152015-05-04 Drug resistance analysis by next generation sequencing in Leishmania Leprohon, Philippe Fernandez-Prada, Christopher Gazanion, Élodie Monte-Neto, Rubens Ouellette, Marc Int J Parasitol Drugs Drug Resist Invited Review The use of next generation sequencing has the power to expedite the identification of drug resistance determinants and biomarkers and was applied successfully to drug resistance studies in Leishmania. This allowed the identification of modulation in gene expression, gene dosage alterations, changes in chromosome copy numbers and single nucleotide polymorphisms that correlated with resistance in Leishmania strains derived from the laboratory and from the field. An impressive heterogeneity at the population level was also observed, individual clones within populations often differing in both genotypes and phenotypes, hence complicating the elucidation of resistance mechanisms. This review summarizes the most recent highlights that whole genome sequencing brought to our understanding of Leishmania drug resistance and likely new directions. Elsevier 2014-09-22 /pmc/articles/PMC4412915/ /pubmed/25941624 http://dx.doi.org/10.1016/j.ijpddr.2014.09.005 Text en © 2014 The Authors http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/3.0/).
spellingShingle Invited Review
Leprohon, Philippe
Fernandez-Prada, Christopher
Gazanion, Élodie
Monte-Neto, Rubens
Ouellette, Marc
Drug resistance analysis by next generation sequencing in Leishmania
title Drug resistance analysis by next generation sequencing in Leishmania
title_full Drug resistance analysis by next generation sequencing in Leishmania
title_fullStr Drug resistance analysis by next generation sequencing in Leishmania
title_full_unstemmed Drug resistance analysis by next generation sequencing in Leishmania
title_short Drug resistance analysis by next generation sequencing in Leishmania
title_sort drug resistance analysis by next generation sequencing in leishmania
topic Invited Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4412915/
https://www.ncbi.nlm.nih.gov/pubmed/25941624
http://dx.doi.org/10.1016/j.ijpddr.2014.09.005
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