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Phylogeography of the second plague pandemic revealed through analysis of historical Yersinia pestis genomes

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Spyrou,  Maria A.
Archaeogenetics, Max Planck Institute for the Science of Human History, Max Planck Society;

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Keller,  Marcel
Archaeogenetics, Max Planck Institute for the Science of Human History, Max Planck Society;

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Tukhbatova,  Rezeda I.
Archaeogenetics, Max Planck Institute for the Science of Human History, Max Planck Society;

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Nelson,  Elizabeth A.
Archaeogenetics, Max Planck Institute for the Science of Human History, Max Planck Society;

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Andrades Valtueña,  Aida
Archaeogenetics, Max Planck Institute for the Science of Human History, Max Planck Society;

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Neumann,  Gunnar
Archaeogenetics, Max Planck Institute for the Science of Human History, Max Planck Society;

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Herbig,  Alexander
Archaeogenetics, Max Planck Institute for the Science of Human History, Max Planck Society;

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Bos,  Kirsten I.
Archaeogenetics, Max Planck Institute for the Science of Human History, Max Planck Society;

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Krause,  Johannes
Archaeogenetics, Max Planck Institute for the Science of Human History, Max Planck Society;

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Citation

Spyrou, M. A., Keller, M., Tukhbatova, R. I., Scheib, C. L., Nelson, E. A., Andrades Valtueña, A., et al. (2019). Phylogeography of the second plague pandemic revealed through analysis of historical Yersinia pestis genomes. Nature Communications, 10(1): 4470. doi:10.1038/s41467-019-12154-0.


Cite as: https://hdl.handle.net/21.11116/0000-0004-D940-F
Abstract
The second plague pandemic, caused by Yersinia pestis, devastated Europe and the nearby regions between the 14th and 18th centuries AD. Here we analyse human remains from ten European archaeological sites spanning this period and reconstruct 34 ancient Y. pestis genomes. Our data support an initial entry of the bacterium through eastern Europe, the absence of genetic diversity during the Black Death, and low within-outbreak diversity thereafter. Analysis of post-Black Death genomes shows the diversification of a Y. pestis lineage into multiple genetically distinct clades that may have given rise to more than one disease reservoir in, or close to, Europe. In addition, we show the loss of a genomic region that includes virulence-related genes in strains associated with late stages of the pandemic. The deletion was also identified in genomes connected with the first plague pandemic (541-750 AD), suggesting a comparable evolutionary trajectory of Y. pestis during both events.