Decoding the sequential program of Chikungunya virus infection

Grant number: 101267860

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Key facts

  • Disease

    Chikungunya
  • Start & end year

    2027
    2031
  • Known Financial Commitments (USD)

    $3,558,844.13
  • Funder

    European Commission
  • Principal Investigator

    Juan REGUERA
  • Research Location

    France
  • Lead Research Institution

    INSTITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICALE
  • Research Priority Alignment

    N/A
  • Research Category

    Pathogen: natural history, transmission and diagnostics
  • Research Subcategory

    Pathogen morphology, shedding & natural history
  • Special Interest Tags

    N/A
  • Study Type

    Non-Clinical
  • Clinical Trial Details

    N/A
  • Broad Policy Alignment

    Pending
  • Age Group

    Not Applicable
  • Vulnerable Population

    Not applicable
  • Occupations of Interest

    Not applicable

Abstract

Viruses are the best cellular biologists; with little genetic information they take control of the infected cell to self-perpetuate and spread worldwide. Understanding how they hijack the cell is complicated by the multifunctional nature of viral components and the large number of cellular factors they interact with. Alphaviruses such as Chikungunya virus have been studied for decades resulting in a plethora of information on host interactors, enzymatic and structural data on single domains or partial complexes. However, these findings provide fragmented snapshots of biological events, disconnected from the reality of infection, where complexes form dynamically over time and in distinct viral organelles. My team has shown how only four non-structural proteins form distinct viral macromolecular complexes carrying out replication in membrane organelles and trapping host factors in cytoplasmic alphagranules. We have now reconstituted in vitro bona fide full replication complexes, as found in the cell, allowing the realistic characterization of replication and host interaction mechanisms. CHIKO aims to provide a precise understanding of the sequence of events in chikungunya virus replication and cell hijacking, from the atomic to the cellular scale, using a broad range of microscopy, biophysical and biochemical techniques to address three challenging questions: Q1: Replication Complex: How do early, medium and late full replication complexes act individually and evolve? Q2: Networking. How do full and partial complexes network with the host factors to hijack the cell and replicate? Q3: In the cell. How similar are the in vitro reconstituted complexes to those found in the infected cell? In what cellular and organelle context do they act and when? The expected outcome is an unprecedented description of viral infection, fundamental for the conception of next generation antivirals, and revealing viral mechanisms with potential applications to RNA based therapies.