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author 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 Luisa
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.
author_facet 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 Luisa
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.
author_sort Pfrengle, Saskia
collection PubMed
description 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. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12915-021-01120-2.
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spelling pubmed-84937302021-10-06 Mycobacterium leprae diversity and population dynamics in medieval Europe from novel ancient genomes 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 Luisa 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. BMC Biol Research Article 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. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12915-021-01120-2. BioMed Central 2021-10-05 /pmc/articles/PMC8493730/ /pubmed/34610848 http://dx.doi.org/10.1186/s12915-021-01120-2 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
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 Luisa
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.
Mycobacterium leprae diversity and population dynamics in medieval Europe from novel ancient genomes
title Mycobacterium leprae diversity and population dynamics in medieval Europe from novel ancient genomes
title_full Mycobacterium leprae diversity and population dynamics in medieval Europe from novel ancient genomes
title_fullStr Mycobacterium leprae diversity and population dynamics in medieval Europe from novel ancient genomes
title_full_unstemmed Mycobacterium leprae diversity and population dynamics in medieval Europe from novel ancient genomes
title_short Mycobacterium leprae diversity and population dynamics in medieval Europe from novel ancient genomes
title_sort mycobacterium leprae diversity and population dynamics in medieval europe from novel ancient genomes
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8493730/
https://www.ncbi.nlm.nih.gov/pubmed/34610848
http://dx.doi.org/10.1186/s12915-021-01120-2
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