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Actin and an unconventional myosin motor, TgMyoF, control the organization and dynamics of the endomembrane network in Toxoplasma gondii

Toxoplasma gondii is an obligate intracellular parasite that relies on three distinct secretory organelles, the micronemes, rhoptries, and dense granules, for parasite survival and disease pathogenesis. Secretory proteins destined for these organelles are synthesized in the endoplasmic reticulum (ER...

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Autores principales: Carmeille, Romain, Schiano Lomoriello, Porfirio, Devarakonda, Parvathi M., Kellermeier, Jacob A., Heaslip, Aoife T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7880465/
https://www.ncbi.nlm.nih.gov/pubmed/33529198
http://dx.doi.org/10.1371/journal.ppat.1008787
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author Carmeille, Romain
Schiano Lomoriello, Porfirio
Devarakonda, Parvathi M.
Kellermeier, Jacob A.
Heaslip, Aoife T.
author_facet Carmeille, Romain
Schiano Lomoriello, Porfirio
Devarakonda, Parvathi M.
Kellermeier, Jacob A.
Heaslip, Aoife T.
author_sort Carmeille, Romain
collection PubMed
description Toxoplasma gondii is an obligate intracellular parasite that relies on three distinct secretory organelles, the micronemes, rhoptries, and dense granules, for parasite survival and disease pathogenesis. Secretory proteins destined for these organelles are synthesized in the endoplasmic reticulum (ER) and sequentially trafficked through a highly polarized endomembrane network that consists of the Golgi and multiple post-Golgi compartments. Currently, little is known about how the parasite cytoskeleton controls the positioning of the organelles in this pathway, or how vesicular cargo is trafficked between organelles. Here we show that F-actin and an unconventional myosin motor, TgMyoF, control the dynamics and organization of the organelles in the secretory pathway, specifically ER tubule movement, apical positioning of the Golgi and post-Golgi compartments, apical positioning of the rhoptries, and finally, the directed transport of Rab6-positive and Rop1-positive vesicles. Thus, this study identifies TgMyoF and actin as the key cytoskeletal components that organize the endomembrane system in T. gondii.
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spelling pubmed-78804652021-02-19 Actin and an unconventional myosin motor, TgMyoF, control the organization and dynamics of the endomembrane network in Toxoplasma gondii Carmeille, Romain Schiano Lomoriello, Porfirio Devarakonda, Parvathi M. Kellermeier, Jacob A. Heaslip, Aoife T. PLoS Pathog Research Article Toxoplasma gondii is an obligate intracellular parasite that relies on three distinct secretory organelles, the micronemes, rhoptries, and dense granules, for parasite survival and disease pathogenesis. Secretory proteins destined for these organelles are synthesized in the endoplasmic reticulum (ER) and sequentially trafficked through a highly polarized endomembrane network that consists of the Golgi and multiple post-Golgi compartments. Currently, little is known about how the parasite cytoskeleton controls the positioning of the organelles in this pathway, or how vesicular cargo is trafficked between organelles. Here we show that F-actin and an unconventional myosin motor, TgMyoF, control the dynamics and organization of the organelles in the secretory pathway, specifically ER tubule movement, apical positioning of the Golgi and post-Golgi compartments, apical positioning of the rhoptries, and finally, the directed transport of Rab6-positive and Rop1-positive vesicles. Thus, this study identifies TgMyoF and actin as the key cytoskeletal components that organize the endomembrane system in T. gondii. Public Library of Science 2021-02-02 /pmc/articles/PMC7880465/ /pubmed/33529198 http://dx.doi.org/10.1371/journal.ppat.1008787 Text en © 2021 Carmeille 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
Carmeille, Romain
Schiano Lomoriello, Porfirio
Devarakonda, Parvathi M.
Kellermeier, Jacob A.
Heaslip, Aoife T.
Actin and an unconventional myosin motor, TgMyoF, control the organization and dynamics of the endomembrane network in Toxoplasma gondii
title Actin and an unconventional myosin motor, TgMyoF, control the organization and dynamics of the endomembrane network in Toxoplasma gondii
title_full Actin and an unconventional myosin motor, TgMyoF, control the organization and dynamics of the endomembrane network in Toxoplasma gondii
title_fullStr Actin and an unconventional myosin motor, TgMyoF, control the organization and dynamics of the endomembrane network in Toxoplasma gondii
title_full_unstemmed Actin and an unconventional myosin motor, TgMyoF, control the organization and dynamics of the endomembrane network in Toxoplasma gondii
title_short Actin and an unconventional myosin motor, TgMyoF, control the organization and dynamics of the endomembrane network in Toxoplasma gondii
title_sort actin and an unconventional myosin motor, tgmyof, control the organization and dynamics of the endomembrane network in toxoplasma gondii
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7880465/
https://www.ncbi.nlm.nih.gov/pubmed/33529198
http://dx.doi.org/10.1371/journal.ppat.1008787
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