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Rhoptry secretion system structure and priming in Plasmodium falciparum revealed using in situ cryo-electron tomography

Apicomplexan parasites secrete contents of the rhoptries, club-shaped organelles in the apical region, into host cells to permit their invasion and establishment of infection. The rhoptry secretory apparatus (RSA), which is critical for rhoptry secretion, was recently discovered in Toxoplasma and Cr...

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Autores principales: Martinez, Matthew, Chen, William David, Cova, Marta Mendonça, Molnár, Petra, Mageswaran, Shrawan Kumar, Guérin, Amandine, John, Audrey R. Odom, Lebrun, Maryse, Chang, Yi-Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7613239/
https://www.ncbi.nlm.nih.gov/pubmed/35817892
http://dx.doi.org/10.1038/s41564-022-01171-3
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author Martinez, Matthew
Chen, William David
Cova, Marta Mendonça
Molnár, Petra
Mageswaran, Shrawan Kumar
Guérin, Amandine
John, Audrey R. Odom
Lebrun, Maryse
Chang, Yi-Wei
author_facet Martinez, Matthew
Chen, William David
Cova, Marta Mendonça
Molnár, Petra
Mageswaran, Shrawan Kumar
Guérin, Amandine
John, Audrey R. Odom
Lebrun, Maryse
Chang, Yi-Wei
author_sort Martinez, Matthew
collection PubMed
description Apicomplexan parasites secrete contents of the rhoptries, club-shaped organelles in the apical region, into host cells to permit their invasion and establishment of infection. The rhoptry secretory apparatus (RSA), which is critical for rhoptry secretion, was recently discovered in Toxoplasma and Cryptosporidium. It is unknown if a similar molecular machinery exists in the malaria parasite Plasmodium. In this study, we use in situ cryo-electron tomography to investigate the rhoptry secretion system in P. falciparum merozoites. We identify the presence of an RSA at the cell apex and a morphologically distinct apical vesicle docking the tips of the two rhoptries to the RSA. We also discover two additional rhoptry organizations that lack the apical vesicle. Using subtomogram averaging, we reveal different conformations of the RSA structure corresponding to different rhoptry organizations. Our results highlight previously unknown steps in the process of rhoptry secretion and indicate a regulatory role for the conserved apical vesicle in host invasion by apicomplexan parasites.
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spelling pubmed-76132392023-01-11 Rhoptry secretion system structure and priming in Plasmodium falciparum revealed using in situ cryo-electron tomography Martinez, Matthew Chen, William David Cova, Marta Mendonça Molnár, Petra Mageswaran, Shrawan Kumar Guérin, Amandine John, Audrey R. Odom Lebrun, Maryse Chang, Yi-Wei Nat Microbiol Article Apicomplexan parasites secrete contents of the rhoptries, club-shaped organelles in the apical region, into host cells to permit their invasion and establishment of infection. The rhoptry secretory apparatus (RSA), which is critical for rhoptry secretion, was recently discovered in Toxoplasma and Cryptosporidium. It is unknown if a similar molecular machinery exists in the malaria parasite Plasmodium. In this study, we use in situ cryo-electron tomography to investigate the rhoptry secretion system in P. falciparum merozoites. We identify the presence of an RSA at the cell apex and a morphologically distinct apical vesicle docking the tips of the two rhoptries to the RSA. We also discover two additional rhoptry organizations that lack the apical vesicle. Using subtomogram averaging, we reveal different conformations of the RSA structure corresponding to different rhoptry organizations. Our results highlight previously unknown steps in the process of rhoptry secretion and indicate a regulatory role for the conserved apical vesicle in host invasion by apicomplexan parasites. 2022-07-11 2022-08 /pmc/articles/PMC7613239/ /pubmed/35817892 http://dx.doi.org/10.1038/s41564-022-01171-3 Text en https://www.springernature.com/gp/open-research/policies/accepted-manuscript-termsUsers may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: https://www.springernature.com/gp/open-research/policies/accepted-manuscript-terms
spellingShingle Article
Martinez, Matthew
Chen, William David
Cova, Marta Mendonça
Molnár, Petra
Mageswaran, Shrawan Kumar
Guérin, Amandine
John, Audrey R. Odom
Lebrun, Maryse
Chang, Yi-Wei
Rhoptry secretion system structure and priming in Plasmodium falciparum revealed using in situ cryo-electron tomography
title Rhoptry secretion system structure and priming in Plasmodium falciparum revealed using in situ cryo-electron tomography
title_full Rhoptry secretion system structure and priming in Plasmodium falciparum revealed using in situ cryo-electron tomography
title_fullStr Rhoptry secretion system structure and priming in Plasmodium falciparum revealed using in situ cryo-electron tomography
title_full_unstemmed Rhoptry secretion system structure and priming in Plasmodium falciparum revealed using in situ cryo-electron tomography
title_short Rhoptry secretion system structure and priming in Plasmodium falciparum revealed using in situ cryo-electron tomography
title_sort rhoptry secretion system structure and priming in plasmodium falciparum revealed using in situ cryo-electron tomography
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7613239/
https://www.ncbi.nlm.nih.gov/pubmed/35817892
http://dx.doi.org/10.1038/s41564-022-01171-3
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