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ToxoPersist SIGNED

Molecular Basis of Toxoplasma gondii Encystation and Persistence

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EC-Contrib. €

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Partnership

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 ToxoPersist project word cloud

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

slow    versatilities    bradyzoites    pv    intracellular    despite    nanosims    resolution    toxoplasma    examination    encystation    capitalize    technologies    biological    barrier    regulatory    blooded    responsible    crispr    network    adaption    molecular    tissue    parasitophorous    pathogenesis    permanent    functions    trafficking    cysts    cw    omics    host    microscopy    muscles    ensures    effectors    immunosuppression    parasitism    nervous    wall    genome    cyst    mechanisms    warm    fast    circuits    pmv    persistence    membrane    rudimentary    hosts    form    vacuole    governing    govern    sensitivity    anticipate    tachyzoites    virtually    immune    convert    bottlenecks    residence    parasite    ex    replicating    unbiased    central    animals    cas9    heart    gondii    poses    cellular    editing    maldi    vivo    threat    striated    defies    maturation    subversion    spectrometry    discoveries    infecting    intervention    mass    ultimately    parasites    onset    clinical    life    initiate    strategies    infection    power    imaging    severe    manifestations    obligate    reactivation    components    immunocompetent    initiates    metabolic    fundamental    successful    encephalitis    pvm    transmission   

Project "ToxoPersist" data sheet

The following table provides information about the project.

Coordinator
UNIVERSITE DE GENEVE 

Organization address
address: RUE DU GENERAL DUFOUR 24
city: GENEVE
postcode: 1211
website: www.unige.ch

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 Switzerland [CH]
 Project website https://www.unige.ch/medecine/mimo/en/groupes/773soldati-favre/g/d/
 Total cost 2˙297˙606 €
 EC max contribution 2˙297˙606 € (100%)
 Programme 1. H2020-EU.1.1. (EXCELLENT SCIENCE - European Research Council (ERC))
 Code Call ERC-2015-AdG
 Funding Scheme ERC-ADG
 Starting year 2016
 Duration (year-month-day) from 2016-10-01   to  2021-09-30

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    UNIVERSITE DE GENEVE CH (GENEVE) coordinator 2˙297˙606.00

Map

 Project objective

Toxoplasma gondii is the most successful obligate intracellular parasites infecting virtually all warm-blooded animals. A infection initiates with the dissemination of the fast-replicating tachyzoites. At the onset of the immune response tachyzoites convert into slow-growing bradyzoites that form cysts in the central nervous system and in striated and heart muscles. Encystation ensures life-long persistence and poses a significant threat of reactivation during immunosuppression and can lead to encephalitis and severe clinical manifestations. Despite the importance of encystation for pathogenesis and transmission, our insight into how T. gondii defies the immune responses to take up permanent residence in the immunocompetent hosts is rudimentary. We propose to determine the molecular mechanisms governing cyst wall formation and parasite adaption to encystation. We will capitalize on the increased sensitivity of -omics approaches, the power of the CRISPR/Cas9 genome editing, the high-resolution microscopy, and on the ex-vivo tissue examination by MALDI imaging mass spectrometry and NanoSIMS technologies.The specific objectives are to: 1. Identify the components of the Cyst Wall (CW), Parasitophorous Vacuole (PV) and PMV Membrane (PVM) of the cyst 2. Determine the parasite factors responsible for CW formation and maturation via targeted and unbiased approaches 3. Define the metabolic network of parasite that is able to initiate encystation and ensure persistence 4. Measure subversion of host metabolic functions by parasite effectors during encystation and persistence We anticipate fundamental discoveries on i) the regulatory and trafficking circuits that govern CW formation as a biological barrier during encystation ii) metabolic adaptation and subversion of host cellular functions during encystation. Ultimately, understanding parasite strategies and versatilities that ensures its parasitism in immunocompetent hosts and bottlenecks as new targets for intervention.

 Publications

year authors and title journal last update
List of publications.
2019 Gaëlle Lentini, David J. Dubois, Bohumil Maco, Dominique Soldati‐Favre, Karine Frénal
The roles of Centrin 2 and Dynein Light Chain 8a in apical secretory organelles discharge of Toxoplasma gondii
published pages: , ISSN: 1398-9219, DOI: 10.1111/tra.12673
Traffic 2019-09-02
2018 Pierre-Mehdi Hammoudi, Bohumil Maco, Sunil Kumar Dogga, Karine Frénal, Dominique Soldati-Favre
Toxoplasma gondii TFP1 is an essential transporter family protein critical for microneme maturation and exocytosis
published pages: , ISSN: 0950-382X, DOI: 10.1111/mmi.13981
Molecular Microbiology 2019-06-13
2017 Pierre-Mehdi Hammoudi, Dominique Soldati-Favre
Insights into the molecular basis of host behaviour manipulation by Toxoplasma gondii infection
published pages: 563-572, ISSN: 2397-8554, DOI: 10.1042/ETLS20170108
Emerging Topics in Life Sciences 1/6 2019-06-13
2018 Hanwei Fang, Ana Rita Gomes, Natacha Klages, Paco Pino, Bohumil Maco, Eloise M. Walker, Zenon A. Zenonos, Fiona Angrisano, Jake Baum, Christian Doerig, David A. Baker, Oliver Billker, Mathieu Brochet
Epistasis studies reveal redundancy among calcium-dependent protein kinases in motility and invasion of malaria parasites
published pages: , ISSN: 2041-1723, DOI: 10.1038/s41467-018-06733-w
Nature Communications 9/1 2019-06-06
2017 Karine Frénal, Damien Jacot, Pierre-Mehdi Hammoudi, Arnault Graindorge, Bohumil Maco, Dominique Soldati-Favre
Myosin-dependent cell-cell communication controls synchronicity of division in acute and chronic stages of Toxoplasma gondii
published pages: 15710, ISSN: 2041-1723, DOI: 10.1038/ncomms15710
Nature Communications 8 2019-06-06

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