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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.

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

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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