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4D analysis of malaria parasite invasion offers insights into erythrocyte membrane remodeling and parasitophorous vacuole formation
Host membrane remodeling is indispensable for viruses, bacteria, and parasites, to subvert the membrane barrier and obtain entry into cells. The malaria parasite Plasmodium spp. induces biophysical and molecular changes to the erythrocyte membrane through the ordered secretion of its apical organell...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8206130/ https://www.ncbi.nlm.nih.gov/pubmed/34131147 http://dx.doi.org/10.1038/s41467-021-23626-7 |
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author | Geoghegan, Niall D. Evelyn, Cindy Whitehead, Lachlan W. Pasternak, Michal McDonald, Phoebe Triglia, Tony Marapana, Danushka S. Kempe, Daryan Thompson, Jennifer K. Mlodzianoski, Michael J. Healer, Julie Biro, Maté Cowman, Alan F. Rogers, Kelly L. |
author_facet | Geoghegan, Niall D. Evelyn, Cindy Whitehead, Lachlan W. Pasternak, Michal McDonald, Phoebe Triglia, Tony Marapana, Danushka S. Kempe, Daryan Thompson, Jennifer K. Mlodzianoski, Michael J. Healer, Julie Biro, Maté Cowman, Alan F. Rogers, Kelly L. |
author_sort | Geoghegan, Niall D. |
collection | PubMed |
description | Host membrane remodeling is indispensable for viruses, bacteria, and parasites, to subvert the membrane barrier and obtain entry into cells. The malaria parasite Plasmodium spp. induces biophysical and molecular changes to the erythrocyte membrane through the ordered secretion of its apical organelles. To understand this process and address the debate regarding how the parasitophorous vacuole membrane (PVM) is formed, we developed an approach using lattice light-sheet microscopy, which enables the parasite interaction with the host cell membrane to be tracked and characterized during invasion. Our results show that the PVM is predominantly formed from the erythrocyte membrane, which undergoes biophysical changes as it is remodeled across all stages of invasion, from pre-invasion through to PVM sealing. This approach enables a functional interrogation of parasite-derived lipids and proteins in PVM biogenesis and echinocytosis during Plasmodium falciparum invasion and promises to yield mechanistic insights regarding how this is more generally orchestrated by other intracellular pathogens. |
format | Online Article Text |
id | pubmed-8206130 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-82061302021-07-01 4D analysis of malaria parasite invasion offers insights into erythrocyte membrane remodeling and parasitophorous vacuole formation Geoghegan, Niall D. Evelyn, Cindy Whitehead, Lachlan W. Pasternak, Michal McDonald, Phoebe Triglia, Tony Marapana, Danushka S. Kempe, Daryan Thompson, Jennifer K. Mlodzianoski, Michael J. Healer, Julie Biro, Maté Cowman, Alan F. Rogers, Kelly L. Nat Commun Article Host membrane remodeling is indispensable for viruses, bacteria, and parasites, to subvert the membrane barrier and obtain entry into cells. The malaria parasite Plasmodium spp. induces biophysical and molecular changes to the erythrocyte membrane through the ordered secretion of its apical organelles. To understand this process and address the debate regarding how the parasitophorous vacuole membrane (PVM) is formed, we developed an approach using lattice light-sheet microscopy, which enables the parasite interaction with the host cell membrane to be tracked and characterized during invasion. Our results show that the PVM is predominantly formed from the erythrocyte membrane, which undergoes biophysical changes as it is remodeled across all stages of invasion, from pre-invasion through to PVM sealing. This approach enables a functional interrogation of parasite-derived lipids and proteins in PVM biogenesis and echinocytosis during Plasmodium falciparum invasion and promises to yield mechanistic insights regarding how this is more generally orchestrated by other intracellular pathogens. Nature Publishing Group UK 2021-06-15 /pmc/articles/PMC8206130/ /pubmed/34131147 http://dx.doi.org/10.1038/s41467-021-23626-7 Text en © Crown 2021 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 Geoghegan, Niall D. Evelyn, Cindy Whitehead, Lachlan W. Pasternak, Michal McDonald, Phoebe Triglia, Tony Marapana, Danushka S. Kempe, Daryan Thompson, Jennifer K. Mlodzianoski, Michael J. Healer, Julie Biro, Maté Cowman, Alan F. Rogers, Kelly L. 4D analysis of malaria parasite invasion offers insights into erythrocyte membrane remodeling and parasitophorous vacuole formation |
title | 4D analysis of malaria parasite invasion offers insights into erythrocyte membrane remodeling and parasitophorous vacuole formation |
title_full | 4D analysis of malaria parasite invasion offers insights into erythrocyte membrane remodeling and parasitophorous vacuole formation |
title_fullStr | 4D analysis of malaria parasite invasion offers insights into erythrocyte membrane remodeling and parasitophorous vacuole formation |
title_full_unstemmed | 4D analysis of malaria parasite invasion offers insights into erythrocyte membrane remodeling and parasitophorous vacuole formation |
title_short | 4D analysis of malaria parasite invasion offers insights into erythrocyte membrane remodeling and parasitophorous vacuole formation |
title_sort | 4d analysis of malaria parasite invasion offers insights into erythrocyte membrane remodeling and parasitophorous vacuole formation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8206130/ https://www.ncbi.nlm.nih.gov/pubmed/34131147 http://dx.doi.org/10.1038/s41467-021-23626-7 |
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