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KissAndSpitRhoptry SIGNED

Unravelling the secretion machinery for virulence factors in apicomplexan parasites

Total Cost €

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EC-Contrib. €

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Partnership

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 KissAndSpitRhoptry project word cloud

Explore the words cloud of the KissAndSpitRhoptry project. It provides you a very rough idea of what is the project "KissAndSpitRhoptry" about.

parasite    disrupt    resolution    depends    question    cells    insights    share    mechanism    export    specialized    secretion    exocytosis    binding    full    hypothesis    conserved    discovery    evolutionarily    global    dissect    genomics    apicomplexan    functions    invasion    advantage    experimental    fusion    free    enigma    control    powerful    questions    toxoplasma    bacteria    disease    cell    trigger    pore    infection    electrophysiology    eukaryotic    relative    equivalent    atomic    blueprint    genetics    ciliate    plasmodium    parasites    plasma    coordinated    mechanisms    cytoplasm    tetrahymena    molecular    model    machinery    obligatory    bacterial    apicomplexa    mechanistic    secretory    contrast    guide    transient    rhoptries    host    effectors    resolved    virulence    employ    expand    attain    efforts    membrane    fundamental    strength    proteins    fascinating    hijack    biochemistry    biological    sense    imaging    explore    answers    living    act    ciliates    secrete    inject    components    assemble    machine    formed    rhoptry    intracellular    organelles    content   

Project "KissAndSpitRhoptry" data sheet

The following table provides information about the project.

Coordinator
INSTITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICALE 

Organization address
address: RUE DE TOLBIAC 101
city: PARIS
postcode: 75654
website: www.inserm.fr

contact info
title: n.a.
name: n.a.
surname: n.a.
function: n.a.
email: n.a.
telephone: n.a.
fax: n.a.

 Coordinator Country France [FR]
 Total cost 2˙496˙210 €
 EC max contribution 2˙496˙210 € (100%)
 Programme 1. H2020-EU.1.1. (EXCELLENT SCIENCE - European Research Council (ERC))
 Code Call ERC-2018-ADG
 Funding Scheme ERC-ADG
 Starting year 2020
 Duration (year-month-day) from 2020-07-01   to  2025-06-30

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    INSTITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICALE FR (PARIS) coordinator 2˙496˙210.00

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 Project objective

Apicomplexan are obligatory intracellular parasites. The ability of these parasites (Plasmodium, Toxoplasma) to cause disease depends on the coordinated secretion of specialized secretory organelles. The rhoptries are particularly important, because they act as the apicomplexan equivalent of bacterial secretion systems. They inject parasite proteins directly in the cytoplasm of host cells not only for invasion but also to hijack host functions crucial to establish and maintain infection. However, in contrast to bacteria where the secretion machinery has been resolved to atomic detail, how eukaryotic parasites secrete and inject rhoptry effectors into cells is an enigma. This proposal aims to dissect the mechanistic steps and the molecular components that assemble the rhoptry secretion machine. Our aims are: 1- To explore the mechanisms that trigger rhoptry exocytosis upon binding of the parasite to the host cell. 2- To provide insights into fusion machinery of rhoptry with the parasite plasma membrane. Our model is based on the discovery that free-living Ciliates and intracellular Apicomplexa share an evolutionarily conserved blueprint for their fusion mechanism. 3- To test and expand our hypothesis that rhoptries deliver their content through a transient pore formed into the host cell membrane. We will employ powerful experimental systems in Toxoplasma, Plasmodium and the Ciliate Tetrahymena, taking full advantage of the relative strength of each model. This comprehensive project will bring together comparative genomics, targeted and global genetics, biochemistry, high resolution imaging and electrophysiology. This project answers a question of fundamental biological importance. How can a parasite sense the host cell and inject virulence factors to attain control? Understanding this mechanism will guide future efforts to disrupt parasite infection and will contribute to broader understanding of fascinating questions of membrane fusion and export processes.

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