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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...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2022
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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. |
format | Online Article Text |
id | pubmed-9283445 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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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