Active Infection & Immunity Genetics & Molecular Biology

Defining viral and human determinants of Dengue virus susceptibility

In plain English

AI plain-English summary

Dengue virus hijacks human cells using proteins that should be stopping it. The virus infects 390 million people each year, causes 20% mortality in severe cases, and has no effective treatments. Climate change is pushing the virus into new populations and closer to its natural reservoir in macaques. Researchers know that restriction factors—proteins that form the first line of antiviral defence—are critical for fighting other viruses, but their role in dengue is poorly understood. This project tests the idea that these same proteins determine whether a dengue infection remains mild or turns deadly. The team will map how 264 restriction factors block dengue replication in human immune cells, identify which viral mutations allow the virus to evade them, and compare genetic variants in restriction factors from patients with mild versus severe disease. They will also test which restriction factors prevent the virus from jumping between macaques and humans. If successful, this work could reveal biomarkers that predict disease severity, improve surveillance of emerging strains, and point toward new treatments. The research is fundamental science—it will not produce a drug tomorrow—but understanding why some people survive dengue while others die is the necessary first step toward changing that outcome.

View original technical description
Dengue virus (DNV) is the world leading mosquito-borne virus and a WHO- priority. With 390 million annual infections, climate change risks infections of naïve populations and spillovers from their macaque natural reservoir. Yet no effective treatments are available. DNV infection causes asymptomatic to severe outcomes with 20% mortality. However, the viral and cellular determinants of dengue outcome remain poorly understood. Restriction factors are proteins that constitute the first line of antiviral defense with major roles in health and disease. In this award, I hypothesize that restriction factors are major determinants of dengue outcome and host range. My preliminary data revealed that 264 restriction factors execute DNV antiviral control in primary human immune cells. We will now 1) Investigate how these restriction factors control DNV replication using computational, virological, and biochemical assays, 2) Identify viral signatures of pathogenicity that enable restriction factor evasion, 3) Define genetic variants in restriction factors present in active cohorts of mild and severe dengue patients, and 4) Identify restriction factors that influence DNV host range using human and macaque ex vivo models. These results will lead to a significant shift in our understanding of DNV immunopathogenesis to inform biomarkers of severity, surveillance, and much needed therapeutics.

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Researchers

Laura Martin-Sancho (EPMC Awardee)

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Original classification

Career Development Award

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