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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.

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

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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