Evolutionary basis of human diseases in western Eurasia: Insights from ancient genomics
In plain English
AI plain-English summaryAncient DNA from human skeletons and long-dead pathogens is being used to trace how past epidemics shaped the genetic vulnerabilities to disease that people in western Eurasia carry today. The problem is that scientists know populations differ in their susceptibility to infections like tuberculosis or autoimmune conditions, but they do not understand why. The evolutionary history behind these differences is largely missing. This project fills that gap by sequencing whole genomes from humans and pathogens that lived over the past 10,000 years—a period that includes the agricultural revolution, the first recorded epidemics, and the rise of cities. By comparing ancient and modern genomes, the team will identify which genetic variants were favoured by natural selection during past disease outbreaks, and catalogue pathogen strains that have since gone extinct. If successful, this is fundamental science that will not produce an immediate treatment or diagnostic. But it will provide a deep evolutionary map of human disease susceptibility and pathogen evolution. That map could eventually inform drug development, improve diagnostic test design, and sharpen global outbreak monitoring by showing which genetic vulnerabilities are ancient and which are recent. Similar fundamental genomic work has already transformed how researchers track emerging infectious diseases.
View original technical description
View the original record at the funder ↗
Researchers
Related Research
Grants with similar aims, by meaning.
Original classification
Collaborative Award in SciencePlain English summaries and category classifications on this site are generated by AI and may not perfectly reflect the original research. Is something wrong? Let us know