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

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

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Resource type
Journal article
Creator (person)
Spyrou, Maria A.
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Keller, Marcel
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Tukhbatova, Rezeda I.
Scheib, Christiana L.
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Nelson, Elizabeth A.
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Date published
October 2, 2019
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.

Funder
Funder nameISNIAwards
Eesti Teadusagentuur
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PRG243
Wellcome Trust
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2000368/Z/15/Z
European Regional Development Fund
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2014-2020.4.01.16-0030
Journal title
Nature Communications
Volume
10
Issue
1
Publisher
Springer Science and Business Media LLC
eISSN
2041-1723
Licence
CC BY 4.0
DOI
10.1038/s41467-019-12154-0
Keywords
General Biochemistry, Genetics and Molecular Biology
General Chemistry
General Physics and Astronomy
Additional information
The Cambridge work is supported by the Wellcome Trust (Award no. 2000368/Z/15/Z) and St. John’s College, Cambridge (J.E.R., T.K., C.C., C.L.S.); the European Union through the European Regional Development Fund (Project No. 2014-2020.4.01.16-0030) (C.L.S.); and the Estonian Research Council personal research grant (PRG243) (C.L.S). M.A.S., M.K., K.I.B. and J.K. were supported by the Max Planck Society and the ERC starting grant APGREID (to J.K.). R.T., A.H. and K.I.B. were supported by the Max Planck Society.
Managed by the British Library and supported by the AHRC

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