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A time-resolved multi-omics atlas of Acanthamoeba castellanii encystment

Encystment is a common stress response of most protists, including free-living amoebae. Cyst formation protects the amoebae from eradication and can increase virulence of the bacteria they harbor. Here, we mapped the global molecular changes that occur in the facultatively pathogenic amoeba Acantham...

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Autores principales: Bernard, Clément, Locard-Paulet, Marie, Noël, Cyril, Duchateau, Magalie, Giai Gianetto, Quentin, Moumen, Bouziane, Rattei, Thomas, Hechard, Yann, Jensen, Lars Juhl, Matondo, Mariette, Samba-Louaka, Ascel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9283445/
https://www.ncbi.nlm.nih.gov/pubmed/35835784
http://dx.doi.org/10.1038/s41467-022-31832-0
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author Bernard, Clément
Locard-Paulet, Marie
Noël, Cyril
Duchateau, Magalie
Giai Gianetto, Quentin
Moumen, Bouziane
Rattei, Thomas
Hechard, Yann
Jensen, Lars Juhl
Matondo, Mariette
Samba-Louaka, Ascel
author_facet Bernard, Clément
Locard-Paulet, Marie
Noël, Cyril
Duchateau, Magalie
Giai Gianetto, Quentin
Moumen, Bouziane
Rattei, Thomas
Hechard, Yann
Jensen, Lars Juhl
Matondo, Mariette
Samba-Louaka, Ascel
author_sort Bernard, Clément
collection PubMed
description Encystment is a common stress response of most protists, including free-living amoebae. Cyst formation protects the amoebae from eradication and can increase virulence of the bacteria they harbor. Here, we mapped the global molecular changes that occur in the facultatively pathogenic amoeba Acanthamoeba castellanii during the early steps of the poorly understood process of encystment. By performing transcriptomic, proteomic, and phosphoproteomic experiments during encystment, we identified more than 150,000 previously undescribed transcripts and thousands of protein sequences absent from the reference genome. These results provide molecular details to the regulation of expected biological processes, such as cell proliferation shutdown, and reveal new insights such as a rapid phospho-regulation of sites involved in cytoskeleton remodeling and translation regulation. This work constitutes the first time-resolved molecular atlas of an encysting organism and a useful resource for further investigation of amoebae encystment to allow for a better control of pathogenic amoebae.
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spelling pubmed-92834452022-07-16 A time-resolved multi-omics atlas of Acanthamoeba castellanii encystment Bernard, Clément Locard-Paulet, Marie Noël, Cyril Duchateau, Magalie Giai Gianetto, Quentin Moumen, Bouziane Rattei, Thomas Hechard, Yann Jensen, Lars Juhl Matondo, Mariette Samba-Louaka, Ascel Nat Commun Article Encystment is a common stress response of most protists, including free-living amoebae. Cyst formation protects the amoebae from eradication and can increase virulence of the bacteria they harbor. Here, we mapped the global molecular changes that occur in the facultatively pathogenic amoeba Acanthamoeba castellanii during the early steps of the poorly understood process of encystment. By performing transcriptomic, proteomic, and phosphoproteomic experiments during encystment, we identified more than 150,000 previously undescribed transcripts and thousands of protein sequences absent from the reference genome. These results provide molecular details to the regulation of expected biological processes, such as cell proliferation shutdown, and reveal new insights such as a rapid phospho-regulation of sites involved in cytoskeleton remodeling and translation regulation. This work constitutes the first time-resolved molecular atlas of an encysting organism and a useful resource for further investigation of amoebae encystment to allow for a better control of pathogenic amoebae. Nature Publishing Group UK 2022-07-14 /pmc/articles/PMC9283445/ /pubmed/35835784 http://dx.doi.org/10.1038/s41467-022-31832-0 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Bernard, Clément
Locard-Paulet, Marie
Noël, Cyril
Duchateau, Magalie
Giai Gianetto, Quentin
Moumen, Bouziane
Rattei, Thomas
Hechard, Yann
Jensen, Lars Juhl
Matondo, Mariette
Samba-Louaka, Ascel
A time-resolved multi-omics atlas of Acanthamoeba castellanii encystment
title A time-resolved multi-omics atlas of Acanthamoeba castellanii encystment
title_full A time-resolved multi-omics atlas of Acanthamoeba castellanii encystment
title_fullStr A time-resolved multi-omics atlas of Acanthamoeba castellanii encystment
title_full_unstemmed A time-resolved multi-omics atlas of Acanthamoeba castellanii encystment
title_short A time-resolved multi-omics atlas of Acanthamoeba castellanii encystment
title_sort time-resolved multi-omics atlas of acanthamoeba castellanii encystment
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9283445/
https://www.ncbi.nlm.nih.gov/pubmed/35835784
http://dx.doi.org/10.1038/s41467-022-31832-0
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