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Evolution of giant pandoravirus revealed by CRISPR/Cas9

Giant viruses (GVs) are a hotspot of unresolved controversies since their discovery, including the definition of “Virus” and their origin. While increasing knowledge of genome diversity has accumulated, GV functional genomics was largely neglected. Here, we describe an experimental framework to gene...

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Autores principales: Bisio, Hugo, Legendre, Matthieu, Giry, Claire, Philippe, Nadege, Alempic, Jean-Marie, Jeudy, Sandra, Abergel, Chantal
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9879987/
https://www.ncbi.nlm.nih.gov/pubmed/36702819
http://dx.doi.org/10.1038/s41467-023-36145-4
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author Bisio, Hugo
Legendre, Matthieu
Giry, Claire
Philippe, Nadege
Alempic, Jean-Marie
Jeudy, Sandra
Abergel, Chantal
author_facet Bisio, Hugo
Legendre, Matthieu
Giry, Claire
Philippe, Nadege
Alempic, Jean-Marie
Jeudy, Sandra
Abergel, Chantal
author_sort Bisio, Hugo
collection PubMed
description Giant viruses (GVs) are a hotspot of unresolved controversies since their discovery, including the definition of “Virus” and their origin. While increasing knowledge of genome diversity has accumulated, GV functional genomics was largely neglected. Here, we describe an experimental framework to genetically modify nuclear GVs and their host Acanthamoeba castellanii using CRISPR/Cas9, shedding light on the evolution from small icosahedral viruses to amphora-shaped GVs. Ablation of the icosahedral major capsid protein in the phylogenetically-related mollivirus highlights a transition in virion shape and size. We additionally demonstrate the existence of a reduced core essential genome in pandoravirus, reminiscent of their proposed smaller ancestors. This proposed genetic expansion led to increased genome robustness, indicating selective pressures for adaptation to uncertain environments. Overall, we introduce new tools for manipulation of the unexplored genome of nuclear GVs and provide experimental evidence suggesting that viral gigantism has aroused as an emerging trait.
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spelling pubmed-98799872023-01-28 Evolution of giant pandoravirus revealed by CRISPR/Cas9 Bisio, Hugo Legendre, Matthieu Giry, Claire Philippe, Nadege Alempic, Jean-Marie Jeudy, Sandra Abergel, Chantal Nat Commun Article Giant viruses (GVs) are a hotspot of unresolved controversies since their discovery, including the definition of “Virus” and their origin. While increasing knowledge of genome diversity has accumulated, GV functional genomics was largely neglected. Here, we describe an experimental framework to genetically modify nuclear GVs and their host Acanthamoeba castellanii using CRISPR/Cas9, shedding light on the evolution from small icosahedral viruses to amphora-shaped GVs. Ablation of the icosahedral major capsid protein in the phylogenetically-related mollivirus highlights a transition in virion shape and size. We additionally demonstrate the existence of a reduced core essential genome in pandoravirus, reminiscent of their proposed smaller ancestors. This proposed genetic expansion led to increased genome robustness, indicating selective pressures for adaptation to uncertain environments. Overall, we introduce new tools for manipulation of the unexplored genome of nuclear GVs and provide experimental evidence suggesting that viral gigantism has aroused as an emerging trait. Nature Publishing Group UK 2023-01-26 /pmc/articles/PMC9879987/ /pubmed/36702819 http://dx.doi.org/10.1038/s41467-023-36145-4 Text en © The Author(s) 2023 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
Bisio, Hugo
Legendre, Matthieu
Giry, Claire
Philippe, Nadege
Alempic, Jean-Marie
Jeudy, Sandra
Abergel, Chantal
Evolution of giant pandoravirus revealed by CRISPR/Cas9
title Evolution of giant pandoravirus revealed by CRISPR/Cas9
title_full Evolution of giant pandoravirus revealed by CRISPR/Cas9
title_fullStr Evolution of giant pandoravirus revealed by CRISPR/Cas9
title_full_unstemmed Evolution of giant pandoravirus revealed by CRISPR/Cas9
title_short Evolution of giant pandoravirus revealed by CRISPR/Cas9
title_sort evolution of giant pandoravirus revealed by crispr/cas9
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9879987/
https://www.ncbi.nlm.nih.gov/pubmed/36702819
http://dx.doi.org/10.1038/s41467-023-36145-4
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