The circadian clock and viral pathogenesis
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AI plain-English summaryA 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.
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