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Expansion microscopy provides new insights into the cytoskeleton of malaria parasites including the conservation of a conoid

Malaria is caused by unicellular Plasmodium parasites. Plasmodium relies on diverse microtubule cytoskeletal structures for its reproduction, multiplication, and dissemination. Due to the small size of this parasite, its cytoskeleton has been primarily observable by electron microscopy (EM). Here, w...

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Autores principales: Bertiaux, Eloïse, Balestra, Aurélia C., Bournonville, Lorène, Louvel, Vincent, Maco, Bohumil, Soldati-Favre, Dominique, Brochet, Mathieu, Guichard, Paul, Hamel, Virginie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7951857/
https://www.ncbi.nlm.nih.gov/pubmed/33705377
http://dx.doi.org/10.1371/journal.pbio.3001020
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author Bertiaux, Eloïse
Balestra, Aurélia C.
Bournonville, Lorène
Louvel, Vincent
Maco, Bohumil
Soldati-Favre, Dominique
Brochet, Mathieu
Guichard, Paul
Hamel, Virginie
author_facet Bertiaux, Eloïse
Balestra, Aurélia C.
Bournonville, Lorène
Louvel, Vincent
Maco, Bohumil
Soldati-Favre, Dominique
Brochet, Mathieu
Guichard, Paul
Hamel, Virginie
author_sort Bertiaux, Eloïse
collection PubMed
description Malaria is caused by unicellular Plasmodium parasites. Plasmodium relies on diverse microtubule cytoskeletal structures for its reproduction, multiplication, and dissemination. Due to the small size of this parasite, its cytoskeleton has been primarily observable by electron microscopy (EM). Here, we demonstrate that the nanoscale cytoskeleton organisation is within reach using ultrastructure expansion microscopy (U-ExM). In developing microgametocytes, U-ExM allows monitoring the dynamic assembly of axonemes and concomitant tubulin polyglutamylation in whole cells. In the invasive merozoite and ookinete forms, U-ExM unveils the diversity across Plasmodium stages and species of the subpellicular microtubule arrays that confer cell rigidity. In ookinetes, we additionally identify an apical tubulin ring (ATR) that colocalises with markers of the conoid in related apicomplexan parasites. This tubulin-containing structure was presumed to be lost in Plasmodium despite its crucial role in motility and invasion in other apicomplexans. Here, U-ExM reveals that a divergent and considerably reduced form of the conoid is actually conserved in Plasmodium species.
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spelling pubmed-79518572021-03-22 Expansion microscopy provides new insights into the cytoskeleton of malaria parasites including the conservation of a conoid Bertiaux, Eloïse Balestra, Aurélia C. Bournonville, Lorène Louvel, Vincent Maco, Bohumil Soldati-Favre, Dominique Brochet, Mathieu Guichard, Paul Hamel, Virginie PLoS Biol Research Article Malaria is caused by unicellular Plasmodium parasites. Plasmodium relies on diverse microtubule cytoskeletal structures for its reproduction, multiplication, and dissemination. Due to the small size of this parasite, its cytoskeleton has been primarily observable by electron microscopy (EM). Here, we demonstrate that the nanoscale cytoskeleton organisation is within reach using ultrastructure expansion microscopy (U-ExM). In developing microgametocytes, U-ExM allows monitoring the dynamic assembly of axonemes and concomitant tubulin polyglutamylation in whole cells. In the invasive merozoite and ookinete forms, U-ExM unveils the diversity across Plasmodium stages and species of the subpellicular microtubule arrays that confer cell rigidity. In ookinetes, we additionally identify an apical tubulin ring (ATR) that colocalises with markers of the conoid in related apicomplexan parasites. This tubulin-containing structure was presumed to be lost in Plasmodium despite its crucial role in motility and invasion in other apicomplexans. Here, U-ExM reveals that a divergent and considerably reduced form of the conoid is actually conserved in Plasmodium species. Public Library of Science 2021-03-11 /pmc/articles/PMC7951857/ /pubmed/33705377 http://dx.doi.org/10.1371/journal.pbio.3001020 Text en © 2021 Bertiaux et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Bertiaux, Eloïse
Balestra, Aurélia C.
Bournonville, Lorène
Louvel, Vincent
Maco, Bohumil
Soldati-Favre, Dominique
Brochet, Mathieu
Guichard, Paul
Hamel, Virginie
Expansion microscopy provides new insights into the cytoskeleton of malaria parasites including the conservation of a conoid
title Expansion microscopy provides new insights into the cytoskeleton of malaria parasites including the conservation of a conoid
title_full Expansion microscopy provides new insights into the cytoskeleton of malaria parasites including the conservation of a conoid
title_fullStr Expansion microscopy provides new insights into the cytoskeleton of malaria parasites including the conservation of a conoid
title_full_unstemmed Expansion microscopy provides new insights into the cytoskeleton of malaria parasites including the conservation of a conoid
title_short Expansion microscopy provides new insights into the cytoskeleton of malaria parasites including the conservation of a conoid
title_sort expansion microscopy provides new insights into the cytoskeleton of malaria parasites including the conservation of a conoid
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7951857/
https://www.ncbi.nlm.nih.gov/pubmed/33705377
http://dx.doi.org/10.1371/journal.pbio.3001020
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