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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.

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

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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