Completed Infection & Immunity Genetics & Molecular Biology

The circadian clock and viral pathogenesis

In plain English

AI plain-English summary

A mouse’s immune response to a herpesvirus or flu virus depends on what time of day it gets infected. The body’s internal 24-hour clock controls many immune functions, and when that clock is disrupted, infections get worse. This project aims to uncover exactly how the circadian clock influences viral pathogenesis at the cellular level. The researcher will use comparative transcriptomics to track which antiviral pathways are active at different times of day and in genetically altered “clock mutant” mice. By ablating or inverting rhythms in candidate pathways, they will test whether time-of-day differences in viral replication arise from rhythms within individual cells or from systemic immune rhythms. They will also compare infections in mice with desynchronised peripheral clocks against tissue-specific clock knockouts in epithelial, myeloid, or lymphocyte cells. This is fundamental science. If it succeeds, it will reveal whether viruses exploit the predictability of host circadian rhythms to time their replication. That mechanistic understanding could eventually inform when antiviral drugs are most effective or how shift work and jet lag might alter susceptibility to infection—but those applications lie well beyond this project’s scope.

View original technical description
Diverse biological processes exhibit circadian rhythms that are driven by cell-autonomous biological clocks, including most facets of the immune response. Using herpesviruses and influenza A virus, I recently demonstrated that circadian rhythms affect virus progression in vivo and replication in cells. Furthermore, I discovered that disruption of circadian rhythms enhances infection. I now want to understand, mechanistically, how the circadian clock influences viral pathogenesis. I will investigate whether cell-intrinsic antiviral pathways are under circadian clock control, using comparative transcriptomics to monitor responses to herpesvirus and influenza A infection at different circadian times and in different ‘clock mutants’. Circadian rhythms in candidate pathways will then be ablated or inverted to assess their impact on time-of-day differences in viral replication in single cells, and as the virus spreads. I will delineate the relative contribution that these endogenous cellular rhythms make to viral pathogenesis, compared with circadian rhythms in systemic host immune responses by examining infection in mice with desynchronised peripheral circadian rhythms compared with tissue-specific ‘clock knockouts’ (arrhythmic epithelial, myeloid-lineage or lymphocyte-lineage mice). Collectively, my research will address the constraints that host circadian rhythms place on viral infection and whether viruses exploit the predictability that biological timekeeping confers upon host physiology.

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Researchers

Rachel Edgar (EPMC Awardee)

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Original classification

Sir Henry Dale Fellowship

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