Completed Infection & Immunity Genetics & Molecular Biology

Evolutionary basis of human diseases in western Eurasia: Insights from ancient genomics

In plain English

AI plain-English summary

Ancient 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
Although large differences in disease susceptibility among present-day human populations have been widely reported, their evolutionary underpinnings remain poorly understood. This project aims to examine how, and to what extent, pathogens shaped disease susceptibility among present-day western Eurasians. We will use whole-genome sequence data from ancient humans and their pathogens to identify novel human genetic variants targeted by past selection, and catalogue novel pathogen variability, including that of now-extinct lineages. Next we will reconstruct the evolutionary history of these newly identified variants and lineages, along with those already known to be associated with disease susceptibility in present-day populations. Finally, we will uncover new associations between human genetic variants and infectious diseases. The focus will be on the last 10,000 years of human history, which encompass some of the greatest changes in our lifestyle, including the agricultural revolution, first known epidemics, and early urbanisation. The proposed study will provide fundamental insights into the evolutionary basis of disease susceptibility in present-day human populations, as well as the evolution of human pathogens. These findings will inform future experimental and clinical research, impact upon current and future healthcare strategies, including the design of diagnostic tests and drug development, and improve global pathogen outbreak monitoring.

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Researchers

Eske Willerslev (EPMC Awardee)Julian Parkhill (EPMC Awardee)Kristian Kristiansen (EPMC Awardee)Laurent Excoffier (EPMC Awardee)Rasmus Nielsen (EPMC Awardee)Richard Durbin (EPMC Awardee)Ron Fouchier (EPMC Awardee)Terry Jones (EPMC Awardee)

Related Research

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Human Adaptation to Changing Diet and Infectious Disease Loads, from the Origins of Agriculture to the Present.

Original classification

Collaborative Award in Science

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