Active Infection & Immunity Genetics & Molecular Biology

MIRACLe: Viewing Multi-segmented Viral RNA Assembly, Infection, and Evolution through the Biomolecular Condensate Lens

In plain English

AI plain-English summary

Rotaviruses kill more than 170,000 children each year, and this project aims to crack open the fundamental mechanism by which these viruses assemble their genomes inside infected cells. Current knowledge of how rotaviruses and other multi-segmented RNA viruses package their genetic material is incomplete. The virus’s genome is split into separate RNA segments, and scientists do not fully understand how the virus selects the right pieces and brings them together. This project will decode the specific structural signals within each RNA segment that govern that selection process, combining experimental data with computational modelling. It will also investigate whether a process called phase separation—where molecules spontaneously form droplet-like structures inside cells—helps build the viral replication factories where assembly happens. If successful, this research will reveal universal rules of genome assembly across a whole class of important pathogens. That deeper understanding could open new avenues for designing antiviral drugs that block assembly, or for engineering better vaccines against rotavirus and related viruses. The work is fundamental science: it does not promise an immediate treatment, but past discoveries about how viruses replicate have repeatedly led to unexpected breakthroughs in medicine.

View original technical description
Rotaviruses are a diverse group of viruses responsible for >170,000 child deaths annually. This project seeks to deepen our understanding of the process by which multi-segmented RNA viruses, including rotaviruses, assemble their genomes. This will be achieved by focusing on three fundamental goals. Firstly, we intend to characterize the role that dynamic RNA structures play in the assembly of rotaviruses. We will decode the specific signals within the RNA that are responsible for selecting different segments, combining insights from experimental structural data and computational modeling. Lastly, we will explore the role of a process known as phase separation in the formation of structures we refer to as viral replication factories. By investigating these mechanisms in rotaviruses and related RNA viruses, we will reveal universal aspects of genome assembly in viruses with segmented genomes. Through these efforts, we will gain transformative insights into the replication cycle of multi-segmented RNA viruses by enhancing our understanding of how they leverage biomolecular condensates during replication, and how their individual RNA structures may shape their evolution. These findings will greatly enhance our knowledge of a large class of important pathogens, providing new avenues for the development of treatments and improved vaccines.

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Researchers

Alexander Borodavka (EPMC Awardee)

Related Research

Grants with similar aims, by meaning.

Uncovering the roles of dynamic RNA interactions during assembly and assortment of multi-segmented viral genomes
Elucidating rotaviral condensate structure and function for future antiviral targeting
Phase transitions underlying viral replication: roles of biomolecular condensates in virus assembly
Structural Biology of RiboNucleoProtein complexes of pathogenic arena and bunyaviruses
Clarifying the role of RNA interactions in RVA genetic stability and evolution

Original classification

Discovery Award

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