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The adaptive roles of aneuploidy and polyclonality in Leishmania in response to environmental stress

Aneuploidy is generally considered harmful, but in some microorganisms, it can act as an adaptive mechanism against environmental stress. Here, we use Leishmania—a protozoan parasite with remarkable genome plasticity—to study the early steps of aneuploidy evolution under high drug pressure (using an...

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Autores principales: Negreira, Gabriel H, de Groote, Robin, Van Giel, Dorien, Monsieurs, Pieter, Maes, Ilse, de Muylder, Geraldine, Van den Broeck, Frederik, Dujardin, Jean‐Claude, Domagalska, Malgorzata A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10481652/
https://www.ncbi.nlm.nih.gov/pubmed/37470283
http://dx.doi.org/10.15252/embr.202357413
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author Negreira, Gabriel H
de Groote, Robin
Van Giel, Dorien
Monsieurs, Pieter
Maes, Ilse
de Muylder, Geraldine
Van den Broeck, Frederik
Dujardin, Jean‐Claude
Domagalska, Malgorzata A
author_facet Negreira, Gabriel H
de Groote, Robin
Van Giel, Dorien
Monsieurs, Pieter
Maes, Ilse
de Muylder, Geraldine
Van den Broeck, Frederik
Dujardin, Jean‐Claude
Domagalska, Malgorzata A
author_sort Negreira, Gabriel H
collection PubMed
description Aneuploidy is generally considered harmful, but in some microorganisms, it can act as an adaptive mechanism against environmental stress. Here, we use Leishmania—a protozoan parasite with remarkable genome plasticity—to study the early steps of aneuploidy evolution under high drug pressure (using antimony or miltefosine as stressors). By combining single‐cell genomics, lineage tracing with cellular barcodes, and longitudinal genome characterization, we reveal that aneuploidy changes under antimony pressure result from polyclonal selection of pre‐existing karyotypes, complemented by further and rapid de novo alterations in chromosome copy number along evolution. In the case of miltefosine, early parasite adaptation is associated with independent point mutations in a miltefosine transporter gene, while aneuploidy changes only emerge later, upon exposure to increased drug levels. Therefore, polyclonality and genome plasticity are hallmarks of parasite adaptation, but the scenario of aneuploidy dynamics depends on the nature and strength of the environmental stress as well as on the existence of other pre‐adaptive mechanisms.
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spelling pubmed-104816522023-09-07 The adaptive roles of aneuploidy and polyclonality in Leishmania in response to environmental stress Negreira, Gabriel H de Groote, Robin Van Giel, Dorien Monsieurs, Pieter Maes, Ilse de Muylder, Geraldine Van den Broeck, Frederik Dujardin, Jean‐Claude Domagalska, Malgorzata A EMBO Rep Reports Aneuploidy is generally considered harmful, but in some microorganisms, it can act as an adaptive mechanism against environmental stress. Here, we use Leishmania—a protozoan parasite with remarkable genome plasticity—to study the early steps of aneuploidy evolution under high drug pressure (using antimony or miltefosine as stressors). By combining single‐cell genomics, lineage tracing with cellular barcodes, and longitudinal genome characterization, we reveal that aneuploidy changes under antimony pressure result from polyclonal selection of pre‐existing karyotypes, complemented by further and rapid de novo alterations in chromosome copy number along evolution. In the case of miltefosine, early parasite adaptation is associated with independent point mutations in a miltefosine transporter gene, while aneuploidy changes only emerge later, upon exposure to increased drug levels. Therefore, polyclonality and genome plasticity are hallmarks of parasite adaptation, but the scenario of aneuploidy dynamics depends on the nature and strength of the environmental stress as well as on the existence of other pre‐adaptive mechanisms. John Wiley and Sons Inc. 2023-07-20 /pmc/articles/PMC10481652/ /pubmed/37470283 http://dx.doi.org/10.15252/embr.202357413 Text en © 2023 The Authors. Published under the terms of the CC BY NC ND 4.0 license. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Reports
Negreira, Gabriel H
de Groote, Robin
Van Giel, Dorien
Monsieurs, Pieter
Maes, Ilse
de Muylder, Geraldine
Van den Broeck, Frederik
Dujardin, Jean‐Claude
Domagalska, Malgorzata A
The adaptive roles of aneuploidy and polyclonality in Leishmania in response to environmental stress
title The adaptive roles of aneuploidy and polyclonality in Leishmania in response to environmental stress
title_full The adaptive roles of aneuploidy and polyclonality in Leishmania in response to environmental stress
title_fullStr The adaptive roles of aneuploidy and polyclonality in Leishmania in response to environmental stress
title_full_unstemmed The adaptive roles of aneuploidy and polyclonality in Leishmania in response to environmental stress
title_short The adaptive roles of aneuploidy and polyclonality in Leishmania in response to environmental stress
title_sort adaptive roles of aneuploidy and polyclonality in leishmania in response to environmental stress
topic Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10481652/
https://www.ncbi.nlm.nih.gov/pubmed/37470283
http://dx.doi.org/10.15252/embr.202357413
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