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Atlas of Plasmodium falciparum intraerythrocytic development using expansion microscopy

Apicomplexan parasites exhibit tremendous diversity in much of their fundamental cell biology, but study of these organisms using light microscopy is often hindered by their small size. Ultrastructural expansion microscopy (U-ExM) is a microscopy preparation method that physically expands the sample...

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Autores principales: Liffner, Benjamin, Cepeda Diaz, Ana Karla, Blauwkamp, James, Anaguano, David, Frölich, Sonja, Muralidharan, Vasant, Wilson, Danny W., Dvorin, Jeffrey, Absalon, Sabrina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10055389/
https://www.ncbi.nlm.nih.gov/pubmed/36993606
http://dx.doi.org/10.1101/2023.03.22.533773
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author Liffner, Benjamin
Cepeda Diaz, Ana Karla
Blauwkamp, James
Anaguano, David
Frölich, Sonja
Muralidharan, Vasant
Wilson, Danny W.
Dvorin, Jeffrey
Absalon, Sabrina
author_facet Liffner, Benjamin
Cepeda Diaz, Ana Karla
Blauwkamp, James
Anaguano, David
Frölich, Sonja
Muralidharan, Vasant
Wilson, Danny W.
Dvorin, Jeffrey
Absalon, Sabrina
author_sort Liffner, Benjamin
collection PubMed
description Apicomplexan parasites exhibit tremendous diversity in much of their fundamental cell biology, but study of these organisms using light microscopy is often hindered by their small size. Ultrastructural expansion microscopy (U-ExM) is a microscopy preparation method that physically expands the sample ~4.5x. Here, we apply U-ExM to the human malaria parasite Plasmodium falciparum during the asexual blood stage of its lifecycle to understand how this parasite is organized in three-dimensions. Using a combination of dye-conjugated reagents and immunostaining, we have catalogued 13 different P. falciparum structures or organelles across the intraerythrocytic development of this parasite and made multiple observations about fundamental parasite cell biology. We describe that the outer centriolar plaque and its associated proteins anchor the nucleus to the parasite plasma membrane during mitosis. Furthermore, the rhoptries, Golgi, basal complex, and inner membrane complex, which form around this anchoring site while nuclei are still dividing, are concurrently segregated and maintain an association to the outer centriolar plaque until the start of segmentation. We also show that the mitochondrion and apicoplast undergo sequential fission events while maintaining an association with the outer centriolar plaque during cytokinesis. Collectively, this study represents the most detailed ultrastructural analysis of P. falciparum during its intraerythrocytic development to date, and sheds light on multiple poorly understood aspects of its organelle biogenesis and fundamental cell biology.
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spelling pubmed-100553892023-03-30 Atlas of Plasmodium falciparum intraerythrocytic development using expansion microscopy Liffner, Benjamin Cepeda Diaz, Ana Karla Blauwkamp, James Anaguano, David Frölich, Sonja Muralidharan, Vasant Wilson, Danny W. Dvorin, Jeffrey Absalon, Sabrina bioRxiv Article Apicomplexan parasites exhibit tremendous diversity in much of their fundamental cell biology, but study of these organisms using light microscopy is often hindered by their small size. Ultrastructural expansion microscopy (U-ExM) is a microscopy preparation method that physically expands the sample ~4.5x. Here, we apply U-ExM to the human malaria parasite Plasmodium falciparum during the asexual blood stage of its lifecycle to understand how this parasite is organized in three-dimensions. Using a combination of dye-conjugated reagents and immunostaining, we have catalogued 13 different P. falciparum structures or organelles across the intraerythrocytic development of this parasite and made multiple observations about fundamental parasite cell biology. We describe that the outer centriolar plaque and its associated proteins anchor the nucleus to the parasite plasma membrane during mitosis. Furthermore, the rhoptries, Golgi, basal complex, and inner membrane complex, which form around this anchoring site while nuclei are still dividing, are concurrently segregated and maintain an association to the outer centriolar plaque until the start of segmentation. We also show that the mitochondrion and apicoplast undergo sequential fission events while maintaining an association with the outer centriolar plaque during cytokinesis. Collectively, this study represents the most detailed ultrastructural analysis of P. falciparum during its intraerythrocytic development to date, and sheds light on multiple poorly understood aspects of its organelle biogenesis and fundamental cell biology. Cold Spring Harbor Laboratory 2023-10-09 /pmc/articles/PMC10055389/ /pubmed/36993606 http://dx.doi.org/10.1101/2023.03.22.533773 Text en https://creativecommons.org/licenses/by/4.0/This work is licensed under a Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/) , which allows reusers to distribute, remix, adapt, and build upon the material in any medium or format, so long as attribution is given to the creator. The license allows for commercial use.
spellingShingle Article
Liffner, Benjamin
Cepeda Diaz, Ana Karla
Blauwkamp, James
Anaguano, David
Frölich, Sonja
Muralidharan, Vasant
Wilson, Danny W.
Dvorin, Jeffrey
Absalon, Sabrina
Atlas of Plasmodium falciparum intraerythrocytic development using expansion microscopy
title Atlas of Plasmodium falciparum intraerythrocytic development using expansion microscopy
title_full Atlas of Plasmodium falciparum intraerythrocytic development using expansion microscopy
title_fullStr Atlas of Plasmodium falciparum intraerythrocytic development using expansion microscopy
title_full_unstemmed Atlas of Plasmodium falciparum intraerythrocytic development using expansion microscopy
title_short Atlas of Plasmodium falciparum intraerythrocytic development using expansion microscopy
title_sort atlas of plasmodium falciparum intraerythrocytic development using expansion microscopy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10055389/
https://www.ncbi.nlm.nih.gov/pubmed/36993606
http://dx.doi.org/10.1101/2023.03.22.533773
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