4.7 Article

Human ancient DNA analyses reveal the high burden of tuberculosis in Europeans over the last 2,000 years

期刊

AMERICAN JOURNAL OF HUMAN GENETICS
卷 108, 期 3, 页码 517-524

出版社

CELL PRESS
DOI: 10.1016/j.ajhg.2021.02.009

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资金

  1. Howard Hughes Medical Institute
  2. Rockefeller University
  3. St. Giles Foundation
  4. National Institutes of Health (NIH) [R01AI088364]
  5. Meyer Foundation
  6. Agence Nationale de la Recherche (ANR) under the Investments for the Future'' program [ANR-10-IAHU-01]
  7. Fondation pour la Recherche Med (FRM) [EQU201903007798]
  8. Institut National de la Santeet de la Recherche Medicale (INSERM)
  9. University of Paris
  10. Institut Pasteur
  11. College de France
  12. Centre Nationale de la Recherche Scientifique (CNRS)
  13. Agence Nationale de la Recherche (ANR) [ANR 17 CE12 0018 02, ANR-19-CE15-0009-02]
  14. French Government's Investissement d'Avenir program [ANR-10-LABX-62-IBEID, ANR-10-LABX-69-01]
  15. Fondation pour la Recherche Medicale (Equipe FRM) [DEQ20180339214]
  16. Fondation Allianz-Institut de France
  17. Fondation de France [00106080]
  18. Imagine Institute
  19. Agence Nationale de la Recherche (ANR) [ANR-17-CE12-0018, ANR-19-CE15-0009] Funding Source: Agence Nationale de la Recherche (ANR)

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This study revealed the history of human exposure to tuberculosis in Europe and found that the TYK2 P1104A variant originated from common ancestors of West Eurasians around 30,000 years ago. The frequency of the variant fluctuated significantly over the past 10,000 years, with a dramatic decrease after the Bronze Age. The drop in frequency was attributed to strong negative selection starting around 2,000 years ago, resulting in a 20% relative fitness reduction in homozygotes, indicating a heavy burden of tuberculosis on European health over the last two millennia.
Tuberculosis (TB), usually caused by Mycobacterium tuberculosis bacteria, is the first cause of death from an infectious disease at the worldwide scale, yet the mode and tempo of TB pressure on humans remain unknown. The recent discovery that homozygotes for the P1104A polymorphism of TYK2 are at higher risk to develop clinical forms of TB provided the first evidence of a common, monogenic predisposition to TB, offering a unique opportunity to inform on human co-evolution with a deadly pathogen. Here, we investigate the history of human exposure to TB by determining the evolutionary trajectory of the TYK2 P1104A variant in Europe, where TB is considered to be the deadliest documented infectious disease. Leveraging a large dataset of 1,013 ancient human genomes and using an approximate Bayesian computation approach, we find that the P1104A variant originated in the common ancestors of West Eurasians similar to 30,000 years ago. Furthermore, we show that, following large-scale population movements of Anatolian Neolithic farmers and Eurasian steppe herders into Europe, P1104A has markedly fluctuated in frequency over the last 10,000 years of European history, with a dramatic decrease in frequency after the Bronze Age. Our analyses indicate that such a frequency drop is attributable to strong negative selection starting similar to 2,000 years ago, with a relative fitness reduction on homozygotes of 20%, among the highest in the human genome. Together, our results provide genetic evidence that TB has imposed a heavy burden on European health over the last two millennia.

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