Decoding the sequential program of Chikungunya virus infection
- Funded by European Commission
- Total publications:0 publications
Grant number: 101267860
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Key facts
Disease
ChikungunyaStart & end year
20272031Known Financial Commitments (USD)
$3,558,844.13Funder
European CommissionPrincipal Investigator
Juan REGUERAResearch Location
FranceLead Research Institution
INSTITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICALEResearch Priority Alignment
N/A
Research Category
Pathogen: natural history, transmission and diagnosticsResearch Subcategory
Pathogen morphology, shedding & natural historySpecial Interest Tags
N/AStudy Type
Non-ClinicalClinical Trial Details
N/ABroad Policy Alignment
PendingAge Group
Not ApplicableVulnerable Population
Not applicableOccupations 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.