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Toxoplasma gondii F-actin forms an extensive filamentous network required for material exchange and parasite maturation

Apicomplexan actin is important during the parasite's life cycle. Its polymerization kinetics are unusual, permitting only short, unstable F-actin filaments. It has not been possible to study actin in vivo and so its physiological roles have remained obscure, leading to models distinct from con...

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Autores principales: Periz, Javier, Whitelaw, Jamie, Harding, Clare, Gras, Simon, Del Rosario Minina, Mario Igor, Latorre-Barragan, Fernanda, Lemgruber, Leandro, Reimer, Madita Alice, Insall, Robert, Heaslip, Aoife, Meissner, Markus
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5375643/
https://www.ncbi.nlm.nih.gov/pubmed/28322189
http://dx.doi.org/10.7554/eLife.24119
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author Periz, Javier
Whitelaw, Jamie
Harding, Clare
Gras, Simon
Del Rosario Minina, Mario Igor
Latorre-Barragan, Fernanda
Lemgruber, Leandro
Reimer, Madita Alice
Insall, Robert
Heaslip, Aoife
Meissner, Markus
author_facet Periz, Javier
Whitelaw, Jamie
Harding, Clare
Gras, Simon
Del Rosario Minina, Mario Igor
Latorre-Barragan, Fernanda
Lemgruber, Leandro
Reimer, Madita Alice
Insall, Robert
Heaslip, Aoife
Meissner, Markus
author_sort Periz, Javier
collection PubMed
description Apicomplexan actin is important during the parasite's life cycle. Its polymerization kinetics are unusual, permitting only short, unstable F-actin filaments. It has not been possible to study actin in vivo and so its physiological roles have remained obscure, leading to models distinct from conventional actin behaviour. Here a modified version of the commercially available actin-chromobody was tested as a novel tool for visualising F-actin dynamics in Toxoplasma gondii. Cb labels filamentous actin structures within the parasite cytosol and labels an extensive F-actin network that connects parasites within the parasitophorous vacuole and allows vesicles to be exchanged between parasites. In the absence of actin, parasites lack a residual body and inter-parasite connections and grow in an asynchronous and disorganized manner. Collectively, these data identify new roles for actin in the intracellular phase of the parasites lytic cycle and provide a robust new tool for imaging parasitic F-actin dynamics. DOI: http://dx.doi.org/10.7554/eLife.24119.001
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spelling pubmed-53756432017-04-05 Toxoplasma gondii F-actin forms an extensive filamentous network required for material exchange and parasite maturation Periz, Javier Whitelaw, Jamie Harding, Clare Gras, Simon Del Rosario Minina, Mario Igor Latorre-Barragan, Fernanda Lemgruber, Leandro Reimer, Madita Alice Insall, Robert Heaslip, Aoife Meissner, Markus eLife Cell Biology Apicomplexan actin is important during the parasite's life cycle. Its polymerization kinetics are unusual, permitting only short, unstable F-actin filaments. It has not been possible to study actin in vivo and so its physiological roles have remained obscure, leading to models distinct from conventional actin behaviour. Here a modified version of the commercially available actin-chromobody was tested as a novel tool for visualising F-actin dynamics in Toxoplasma gondii. Cb labels filamentous actin structures within the parasite cytosol and labels an extensive F-actin network that connects parasites within the parasitophorous vacuole and allows vesicles to be exchanged between parasites. In the absence of actin, parasites lack a residual body and inter-parasite connections and grow in an asynchronous and disorganized manner. Collectively, these data identify new roles for actin in the intracellular phase of the parasites lytic cycle and provide a robust new tool for imaging parasitic F-actin dynamics. DOI: http://dx.doi.org/10.7554/eLife.24119.001 eLife Sciences Publications, Ltd 2017-03-21 /pmc/articles/PMC5375643/ /pubmed/28322189 http://dx.doi.org/10.7554/eLife.24119 Text en © 2017, Periz et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Cell Biology
Periz, Javier
Whitelaw, Jamie
Harding, Clare
Gras, Simon
Del Rosario Minina, Mario Igor
Latorre-Barragan, Fernanda
Lemgruber, Leandro
Reimer, Madita Alice
Insall, Robert
Heaslip, Aoife
Meissner, Markus
Toxoplasma gondii F-actin forms an extensive filamentous network required for material exchange and parasite maturation
title Toxoplasma gondii F-actin forms an extensive filamentous network required for material exchange and parasite maturation
title_full Toxoplasma gondii F-actin forms an extensive filamentous network required for material exchange and parasite maturation
title_fullStr Toxoplasma gondii F-actin forms an extensive filamentous network required for material exchange and parasite maturation
title_full_unstemmed Toxoplasma gondii F-actin forms an extensive filamentous network required for material exchange and parasite maturation
title_short Toxoplasma gondii F-actin forms an extensive filamentous network required for material exchange and parasite maturation
title_sort toxoplasma gondii f-actin forms an extensive filamentous network required for material exchange and parasite maturation
topic Cell Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5375643/
https://www.ncbi.nlm.nih.gov/pubmed/28322189
http://dx.doi.org/10.7554/eLife.24119
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