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RESTRIVIR SIGNED

Characterization of a novel mechanism restricting virus infection in reproductive tissues

Total Cost €

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EC-Contrib. €

0

Partnership

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 RESTRIVIR project word cloud

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

interference    stress    melanogaster    viral    sirna    like    fruitfly    gfp    tract    screens    virus    line    house    candidate    laboratory    rnai    partial    replication    resequencing    surrounding    controls    replicon    genetic    completely    detected    followed    oss    host    restriction    mammals    reproductive    differentially    expressed    reverse    follicular    identification    uncover    derepressed    viruses    responsible    permissive    pirna    flock    derepression    acts    worldwide    lines    genes    ems    transposon    gene    combination    mutants    screening    germline    health    sort    fhv    mobilization    mutagenesis    shrna    cell    innate    pirnas    ex    tissues    restrictive    human    rna    mutant    defense    expression    arthropod    provides    cells    expressing    mechanism    decipher    except    monolayer    transformed    antiviral    b2    potent    infected    immunity    fc    borne    implications    restricting    insects    scientific    fcs    vivo    genome    defenses    sequencing    characterization    origin    delta    somatic    protect    tested    drosophila    function   

Project "RESTRIVIR" data sheet

The following table provides information about the project.

Coordinator
CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE CNRS 

Organization address
address: RUE MICHEL ANGE 3
city: PARIS
postcode: 75794
website: www.cnrs.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]
 Project website http://ibmc-m3i.cnrs.fr/en/research-groups/antiviral-immunity/
 Total cost 185˙076 €
 EC max contribution 185˙076 € (100%)
 Programme 1. H2020-EU.1.3.2. (Nurturing excellence by means of cross-border and cross-sector mobility)
 Code Call H2020-MSCA-IF-2015
 Funding Scheme MSCA-IF-EF-ST
 Starting year 2016
 Duration (year-month-day) from 2016-04-01   to  2018-03-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE CNRS FR (PARIS) coordinator 185˙076.00

Map

 Project objective

Like mammals, insects are infected by many viruses. Among them, arthropod-borne viruses are an increasing worldwide health concern. Insects have potent innate antiviral defenses, of which RNA interference (RNAi) is the main and best studied. In the fruitfly Drosophila melanogaster, the siRNA pathway controls viral replication in somatic tissues. The piRNA pathway, another RNAi based response, acts specifically in the reproductive tract (germline and follicular cells (FC), a monolayer of somatic cells surrounding the germline), to protect the genome against transposon mobilization. Other innate immunity or stress pathways also contribute to the antiviral defense. The host laboratory obtained evidence for a new mechanism controlling viral replication in the FCs of Drosophila. Indeed, a viral replicon derived from Flock House Virus and expressing GFP (FHVΔB2-GFP) is completely derepressed in somatic tissues of mutants for the siRNA pathway, except in FCs, where derepression is partial. No piRNAs of viral origin can be detected in these cells. This viral replicon provides a unique system to decipher a novel pathway restricting viral replication. For this, I will use a combination of forward and reverse genetic screens. EMS mutagenesis, screening for GFP expression and genome resequencing will be used to uncover genes responsible for restricting the replicon in FCs. Next, I will use GFP expression to sort restrictive and permissive FCs in a siRNA pathway mutant followed by RNA sequencing to identify differentially expressed genes. The function of the identified genes will be tested in vivo, using shRNA Drosophila lines. Finally, OSS cells, an FC-derived cell line, will be transformed with the FHVΔB2-GFP replicon to evaluate candidate gene function ex vivo. The identification and characterization of genes involved in a novel viral restriction pathway will increase the knowledge about innate antiviral immunity, an important scientific topic with human health implications.

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The information about "RESTRIVIR" are provided by the European Opendata Portal: CORDIS opendata.

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