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

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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.

In: Nature Communications, Vol. 13, No. 1, 4104, 2022.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Bernard, C, Locard-Paulet, M, Noël, C, Duchateau, M, Giai Gianetto, Q, Moumen, B, Rattei, T, Hechard, Y, Jensen, LJ, Matondo, M & Samba-Louaka, A 2022, 'A time-resolved multi-omics atlas of Acanthamoeba castellanii encystment', Nature Communications, vol. 13, no. 1, 4104. https://doi.org/10.1038/s41467-022-31832-0

APA

Bernard, C., Locard-Paulet, M., Noël, C., Duchateau, M., Giai Gianetto, Q., Moumen, B., Rattei, T., Hechard, Y., Jensen, L. J., Matondo, M., & Samba-Louaka, A. (2022). A time-resolved multi-omics atlas of Acanthamoeba castellanii encystment. Nature Communications, 13(1), [4104]. https://doi.org/10.1038/s41467-022-31832-0

Vancouver

Bernard C, Locard-Paulet M, Noël C, Duchateau M, Giai Gianetto Q, Moumen B et al. A time-resolved multi-omics atlas of Acanthamoeba castellanii encystment. Nature Communications. 2022;13(1). 4104. https://doi.org/10.1038/s41467-022-31832-0

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. / A time-resolved multi-omics atlas of Acanthamoeba castellanii encystment. In: Nature Communications. 2022 ; Vol. 13, No. 1.

Bibtex

@article{4cffc89a9edd4eaca0251e16cd43430b,
title = "A time-resolved multi-omics atlas of Acanthamoeba castellanii encystment",
abstract = "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.",
author = "Cl{\'e}ment Bernard and Marie Locard-Paulet and Cyril No{\"e}l and Magalie Duchateau and {Giai Gianetto}, Quentin and Bouziane Moumen and Thomas Rattei and Yann Hechard and Jensen, {Lars Juhl} and Mariette Matondo and Ascel Samba-Louaka",
note = "Publisher Copyright: {\textcopyright} 2022, The Author(s).",
year = "2022",
doi = "10.1038/s41467-022-31832-0",
language = "English",
volume = "13",
journal = "Nature Communications",
issn = "2041-1723",
publisher = "nature publishing group",
number = "1",

}

RIS

TY - JOUR

T1 - A time-resolved multi-omics atlas of Acanthamoeba castellanii encystment

AU - Bernard, Clément

AU - Locard-Paulet, Marie

AU - Noël, Cyril

AU - Duchateau, Magalie

AU - Giai Gianetto, Quentin

AU - Moumen, Bouziane

AU - Rattei, Thomas

AU - Hechard, Yann

AU - Jensen, Lars Juhl

AU - Matondo, Mariette

AU - Samba-Louaka, Ascel

N1 - Publisher Copyright: © 2022, The Author(s).

PY - 2022

Y1 - 2022

N2 - 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.

AB - 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.

U2 - 10.1038/s41467-022-31832-0

DO - 10.1038/s41467-022-31832-0

M3 - Journal article

C2 - 35835784

AN - SCOPUS:85134145889

VL - 13

JO - Nature Communications

JF - Nature Communications

SN - 2041-1723

IS - 1

M1 - 4104

ER -

ID: 314631161