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Ancient DNA study provides clues to leprosy susceptibility in medieval Europe

Sarah A. Inskip, Gökhan Mustafa Yazıcı, Ruoyun Hui et al.

14 Authors
2024-02-06 Published
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

SA
Sarah A. Inskip
GM
Gökhan Mustafa Yazıcı
RH
Ruoyun Hui
RR
Robin R. Larsen
ST
Sahra Talamo
JL
Jesper L. Boldsen
NL
Niels Lynnerup
SM
Simon Mays
CD
Carney D. Matheson
GM
G. Michael Taylor
HD
Helen D. Donoghue
ST
Stewart T. Cole
JK
Johannes Krause
BK
Ben Krause-Kyora
Chapter II

Abstract

Summary of the research findings

Leprosy was one of the most feared diseases in medieval Europe, yet the reasons for its subsequent decline remain unclear. Here we present an ancient DNA study of 92 individuals from five medieval leprosy hospitals (leprosaria) across England and Denmark (ca. 1200-1400 CE) and 273 contemporaneous non-leprosy controls. We recovered 25 ancient Mycobacterium leprae genomes and identified a new ancient lineage. Comparison with modern M. leprae diversity suggests that medieval European strains contributed to the modern global distribution. We also generated human genomic data and identified five loci significantly associated with leprosy susceptibility, including novel associations at LACC1 and IRF8. These variants show strong geographic structure, with four protective variants significantly more common in Northern Europeans. Combined with bioarchaeological evidence, our results suggest that selective pressure from M. leprae may have contributed to regional differences in immune gene frequencies, potentially explaining the disease's decline in Europe.

Chapter III

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AI-generated by DNAGENICS

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Important: This summary is AI-generated by DNAGENICS for informational purposes only. It was not created by, affiliated with, or endorsed by the researchers behind the original publication, and is based solely on that published research. It may contain errors or omissions. DNAGENICS disclaims all liability for any inaccuracies or consequences arising from use of this information. Verify all information against the original publication. This is not professional scientific review or medical advice.

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