Please use this identifier to cite or link to this item: http://hdl.handle.net/10174/31541

Title: Mycobacterium leprae diversity and population dynamics in medieval Europe from novel ancient genomes.
Authors: Pfrengle, Saskia
Neukamm, Judith
Guellil, Meriam
Keller, Marcel
Molak, Martyna
Avanzi, Charlotte
Kushniarevich, Alena
Montes, Núria
Neumann, Gunnar U.
Reiter, Ella
Tukhbatova, Rezeda I.
Berezina, Nataliya Y.
Buzhilova, Alexandra P.
Korobov, Dmitry S
Suppersberger Hamre, Stian
Matos, Vitor M J
Ferreira, Maria T
González-Garrido, Laura
Wasterlain, Sofia N
Lopes, Célia
Santos, Ana Luísa
Antunes-Ferreira, Nathalie
Duarte, Vitória
Silva, Ana Maria
Melo, Linda
Sarkic, Natasa
Saag, Lehti
Tambets, Kristiina
Busso, Philippe
Cole, Stewart T
Avlasovich, Alexei
Roberts, Charlotte A
Sheridan, Alison
Cessford, Craig
Robb, John
Krause, Johannes
Scheib, Christiana L
Inskip, Sarah A
Schuenemann, Verena J
Keywords: Ancient DNA
Ancient pathogen genomics
Leprosaria
Mycobacterium leprae
Paleomicrobiology
Paleopathology
Pathogen diversity
Pathogen population dynamics
Issue Date: 5-Oct-2021
Publisher: BMC Biology
Citation: Pfrengle, S., Neukamm, J., Guellil, M. et al. Mycobacterium leprae diversity and population dynamics in medieval Europe from novel ancient genomes. BMC Biol 19, 220 (2021). https://doi.org/10.1186/s12915-021-01120-2
Abstract: BACKGROUND: Hansen's disease (leprosy), widespread in medieval Europe, is today mainly prevalent in tropical and subtropical regions with around 200,000 new cases reported annually. Despite its long history and appearance in historical records, its origins and past dissemination patterns are still widely unknown. Applying ancient DNA approaches to its major causative agent, Mycobacterium leprae, can significantly improve our understanding of the disease's complex history. Previous studies have identified a high genetic continuity of the pathogen over the last 1500 years and the existence of at least four M. leprae lineages in some parts of Europe since the Early Medieval period. RESULTS: Here, we reconstructed 19 ancient M. leprae genomes to further investigate M. leprae's genetic variation in Europe, with a dedicated focus on bacterial genomes from previously unstudied regions (Belarus, Iberia, Russia, Scotland), from multiple sites in a single region (Cambridgeshire, England), and from two Iberian leprosaria. Overall, our data confirm the existence of similar phylogeographic patterns across Europe, including high diversity in leprosaria. Further, we identified a new genotype in Belarus. By doubling the number of complete ancient M. leprae genomes, our results improve our knowledge of the past phylogeography of M. leprae and reveal a particularly high M. leprae diversity in European medieval leprosaria. CONCLUSIONS: Our findings allow us to detect similar patterns of strain diversity across Europe with branch 3 as the most common branch and the leprosaria as centers for high diversity. The higher resolution of our phylogeny tree also refined our understanding of the interspecies transfer between red squirrels and humans pointing to a late antique/early medieval transmission. Furthermore, with our new estimates on the past population diversity of M. leprae, we gained first insights into the disease's global history in relation to major historic events such as the Roman expansion or the beginning of the regular transatlantic long distance trade. In summary, our findings highlight how studying ancient M. leprae genomes worldwide improves our understanding of leprosy's global history and can contribute to current models of M. leprae's worldwide dissemination, including interspecies transmissions.
URI: https://bmcbiol.biomedcentral.com/articles/10.1186/s12915-021-01120-2
http://hdl.handle.net/10174/31541
Type: article
Appears in Collections:BIO - Publicações - Artigos em Revistas Internacionais Com Arbitragem Científica

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