Exploring the Prokaryotic-Eukaryotic Conservation of Antiviral immunity: from bacterial immune systems to novel antiviral drugs

This project aims to map bacterial antiviral immunity and discover novel anti-phage compounds, potentially transforming our understanding of prokaryotic immune systems and leading to new antiviral therapies.

Subsidie
€ 1.496.500
2022

Projectdetails

Introduction

Bacteria have evolved multiple lines of defense against their viruses, bacteriophages. Such weapons include restriction modification and CRISPR systems that have greatly impacted biomedical research. Studies aimed at uncovering novel defense mechanisms describe an unsuspected diversity of anti-phage systems, spanning thousands of protein families. Several of these anti-phage systems, such as prokaryotic viperins, appear to be ancestors of major eukaryotic antiviral pathways. This striking conservation between eukaryotic and prokaryotic immunity leads me to two hypotheses on which the present proposal is based.

Hypothesis 1: Organization of Antiviral Immunity

First, I postulate that the organization of antiviral immunity in eukaryotes as an immune system, i.e., an integrated network of various antiviral mechanisms, might be conserved in prokaryotes. This implies that each anti-phage system does not act in isolation but is rather part of a whole, the bacterial immune system.

Research Approach

To explore this hypothesis, I will:

  1. Characterize the distribution of known anti-phage systems encoded in prokaryotic genomes.
  2. Explore the potential synergies and co-regulation existing between these systems.

I thereby aim to build an integrated map of bacterial antiviral immunity.

Hypothesis 2: Additional Anti-Phage Compounds

Second, I hypothesize that prokaryotes produce additional small anti-phage compounds, such as the viperin products, with a potential activity against eukaryotic viruses.

Research Approach

To explore this idea, I will:

  1. Study the molecular mechanisms of the viperin family.
  2. Use genomics to predict novel chemical-based anti-phage systems.
  3. Follow up with their experimental characterizations.

These projects could lead to the identification of novel antiviral molecules that could be further harnessed in the clinic.

Conclusion

Overall, I expect this proposal to generate new knowledge that will have the potential to radically change our view on the immune systems of prokaryotes and provide new therapeutic leads.

Financiële details & Tijdlijn

Financiële details

Subsidiebedrag€ 1.496.500
Totale projectbegroting€ 1.496.500

Tijdlijn

Startdatum1-10-2022
Einddatum30-9-2027
Subsidiejaar2022

Partners & Locaties

Projectpartners

  • INSTITUT PASTEURpenvoerder
  • INSTITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICALE

Land(en)

France

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