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ToxoPersist SIGNED

Molecular Basis of Toxoplasma gondii Encystation and Persistence

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EC-Contrib. €

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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.

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

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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