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

Author:

Periz Javier1,Whitelaw Jamie1,Harding Clare1,Gras Simon1,Del Rosario Minina Mario Igor1,Latorre-Barragan Fernanda1,Lemgruber Leandro1,Reimer Madita Alice1,Insall Robert2,Heaslip Aoife3,Meissner Markus1ORCID

Affiliation:

1. Wellcome Centre for Molecular Parasitology, Institute of Infection, Immunity & Inflammation, University of Glasgow, Glasgow, United Kingdom

2. Cancer Research United Kingdom Beatson Institute, Bearsden, United Kingdom

3. Department of Molecular Physiology and Biophysics, University of Vermont, Burlington, United States

Abstract

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.

Funder

Wellcome

H2020 European Research Council

National Institute for Health Research

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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