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A draft genome of Yersinia pestis from victims of the Black Death

Bos, Kirsten I., Schuenemann, Verena J., Golding, G. Brian, Burbano, Hernán A., Waglechner, Nicholas, Coombes, Brian K., McPhee, Joseph B., DeWitte, Sharon N., Meyer, Matthias, Schmedes, Sarah, Wood, James, Earn, David J. D., Herring, D. Ann, Bauer, Peter, Poinar, Hendrik N., Krause, Johannes·2011·Nature

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  • Analyses of the victims of both the Plague of Justinian and the Black Death have shown that Y. pestis was indeed the cause of both pandemics, and further genomic analysis has provided insight into the course of these pandemics over time, including parallel changes in the pathogen itself.

    “For example, analyses of the victims of both the Plague of Justinian and the Black Death have shown that Y. pestis was indeed the cause of both pandemics 65,303 , and further genomic analysis has provided insight into the course of these pandemics over time, including parallel changes in the pathogen itself [304][305][306] .”

    From Ancient DNA analysis (2021) · cites this paper as [65]

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  1. Stoneking, M. & Krause, J. Learning about human population history from ancient and modern genomes. Nature Rev. Genet. 12, 603–614 (2011) · DOI
  2. Haensch, S. et al. Distinct clones of Yersinia pestis caused the Black Death. PLoS Pathog. 6, e1001134 (2010) · DOI
  3. Schuenemann, V. J. et al. Targeted enrichment of ancient pathogens yielding the pPCP1 plasmid of Yersinia pestis from victims of the Black Death. Proc. Natl Acad. Sci. USA 10.1073/pnas.1105107108 (29 August, 2011). · DOI
  4. Benedictow, O. J. The Black Death 1346–1353: The Complete History (Boydell Press, 2004)
  5. Scott, S. & Duncan, C. J. Biology of Plagues (Cambridge Univ. Press, 2001) · DOI
  6. Cohn, S. K. The Black Death Transformed: Disease and Culture in Early Renaissance Europe (Arnold Publication, 2003)
  7. Briggs, A. W. et al. Patterns of damage in genomic DNA sequences from a Neandertal. Proc. Natl Acad. Sci. USA 104, 14616–14621 (2007) · DOI · Paper page
  8. Hodges, E. et al. Hybrid selection of discrete genomic intervals on custom-designed microarrays for massively parallel sequencing. Nature Protocols 4, 960–974 (2009) · DOI
  9. Green, R. E. et al. A complete Neandertal mitochondrial genome sequence determined by high-throughput sequencing. Cell 134, 416–426 (2008) · DOI
  10. Chain, P. S. G. et al. Insights into the evolution of Yersinia pestis through whole-genome comparison with Yersinia pseudotuberculosis. Proc. Natl Acad. Sci. USA 101, 13826–13831 (2004) · DOI
  11. Achtman, M. et al. Microevolution and history of the plague bacillus, Yersinia pestis. Proc. Natl Acad. Sci. USA 101, 17837–17842 (2004) · DOI
  12. Morelli, G. et al. Yersinia pestis genome sequencing identifies patterns of global phylogenetic diversity. Nature Genet. 42, 1140–1143 (2010) · DOI
  13. Harris, S. R. et al. Evolution of MRSA during hospital transmission and intercontinental spread. Science 327, 469–474 (2010) · DOI
  14. Song, Y. et al. Complete genome sequence of Yersinia pestis strain 91001, an isolate avirulent to humans. DNA Res. 11, 179–197 (2004) · DOI
  15. Eppinger, M. et al. Draft genome sequences of Yersinia pestis isolates from natural foci of endemic plague in China. J. Bacteriol. 191, 7628–7629 (2009) · DOI
  16. Pouillot, F., Fayolle, C. & Carniel, E. Characterization of chromosomal regions conserved in Yersinia pseudotuberculosis and lost by Yersinia pestis. Infect. Immun. 76, 4592–4599 (2008) · DOI
  17. Stenseth, N. C. et al. Plague: past, present, and future. PLoS Med. 5, e3 (2008) · DOI
  18. Baum, J. & Bar-Gal, G. K. in Emerging Pathogens Archaeology, Ecology & Evolution of Infectious Diseases (eds Greenblat, C. L. & Spigleman, M. ) 67–78 (Oxford Univ. Press, 2003) · DOI
  19. Brown, N. F. et al. Crossing the line: selection and evolution of virulence traits. PLoS Pathog. 2, e42 (2006) · DOI
  20. Wood, J. W., Ferrell, R. J. & DeWitte-Aviña, S. N. The temporal dynamics of the fourteenth-century Black Death: new evidence from ecclesiastical records. Hum. Biol. 75, 427–448 (2003) · DOI
  21. Joosten, M. H. A. J., Cosijnsen, T. J. & De Wit, P. J. G. Host resistance to a fungal tomato pathogen lost by a single base pair change in an avirulence gene. Nature 367, 384–386 (1994) · DOI
  22. Xu, L. et al. Nonlinear effect of climate on plague during the third pandemic in China. Proc. Natl Acad. Sci. USA (2011) · DOI
  23. Keeling, M. K. & Gilligan, C. A. Metapopulation dynamics of bubonic plague. Nature 407, 903–906 (2000) · DOI
  24. Barrett, R., Kuzawa, C. W., McDade, T. & Armelagos, G. J. Emerging and re-emerging infectious diseases: the third epidemiologic transition. Annu. Rev. Anthropol. 27, 247–271 (1998) · DOI
  25. Singer, M. & Clair, S. Syndemics and public health: reconceptualizing disease in bio-social context. Med. Anthropol. Q. 17, 423–441 (2003) · DOI · Paper page

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Metadata

Authors
Bos, K. I., Schuenemann, V. J., Golding, G. B., Burbano, H. A., Waglechner, N., Coombes, B. K., McPhee, J. B., DeWitte, S. N., Meyer, M., Schmedes, S., Wood, J., Earn, D. J. D., Herring, D. A., Bauer, P., Poinar, H. N., & Krause, J.
Venue
Nature
Published
2011-10-12
Volume
478
Issue
7370
Pages
506-510
ISSN
  • 0028-0836
  • 1476-4687
Cited by
619
References
1
Language
en
Update notices
erratum (2011-12-08)

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