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      Distinct Clones of Yersinia pestis Caused the Black Death

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          Abstract

          From AD 1347 to AD 1353, the Black Death killed tens of millions of people in Europe, leaving misery and devastation in its wake, with successive epidemics ravaging the continent until the 18 th century. The etiology of this disease has remained highly controversial, ranging from claims based on genetics and the historical descriptions of symptoms that it was caused by Yersinia pestis to conclusions that it must have been caused by other pathogens. It has also been disputed whether plague had the same etiology in northern and southern Europe. Here we identified DNA and protein signatures specific for Y. pestis in human skeletons from mass graves in northern, central and southern Europe that were associated archaeologically with the Black Death and subsequent resurgences. We confirm that Y. pestis caused the Black Death and later epidemics on the entire European continent over the course of four centuries. Furthermore, on the basis of 17 single nucleotide polymorphisms plus the absence of a deletion in glpD gene, our aDNA results identified two previously unknown but related clades of Y. pestis associated with distinct medieval mass graves. These findings suggest that plague was imported to Europe on two or more occasions, each following a distinct route. These two clades are ancestral to modern isolates of Y. pestis biovars Orientalis and Medievalis. Our results clarify the etiology of the Black Death and provide a paradigm for a detailed historical reconstruction of the infection routes followed by this disease.

          Author Summary

          Several historical epidemic waves of plague have been attributed to Yersinia pestis, the etiologic agent of modern plague. The most famous of these was the second pandemic which was active in Europe from AD 1347 until 1750, and began with the ‘Black Death’. The most informative method to establish the etiological nature of these ancient infections should be the analysis of ancient DNA, but the results of this method have been controversial. Here, by combining ancient DNA analyses and protein-specific detection, we demonstrate unambiguously that Y. pestis caused the Black Death. Furthermore, we show that at least two variants of Y. pestis spread over Europe during the second pandemic. The analysis of up to 20 diagnostic markers reveals that the two variants evolved near the time that phylogenetic branches 1 and 2 separated and may no longer exist. Our results thus resolve a long-standing debate about the etiology of the Black Death and provide key information about the evolution of the plague bacillus and the spread of the disease during the Middle Ages.

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          Most cited references30

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          Yersinia pestis--etiologic agent of plague.

          Plague is a widespread zoonotic disease that is caused by Yersinia pestis and has had devastating effects on the human population throughout history. Disappearance of the disease is unlikely due to the wide range of mammalian hosts and their attendant fleas. The flea/rodent life cycle of Y. pestis, a gram-negative obligate pathogen, exposes it to very different environmental conditions and has resulted in some novel traits facilitating transmission and infection. Studies characterizing virulence determinants of Y. pestis have identified novel mechanisms for overcoming host defenses. Regulatory systems controlling the expression of some of these virulence factors have proven quite complex. These areas of research have provide new insights into the host-parasite relationship. This review will update our present understanding of the history, etiology, epidemiology, clinical aspects, and public health issues of plague.
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            Yersinia pestis, the cause of plague, is a recently emerged clone of Yersinia pseudotuberculosis.

            Plague, one of the most devastating diseases of human history, is caused by Yersinia pestis. In this study, we analyzed the population genetic structure of Y. pestis and the two other pathogenic Yersinia species, Y. pseudotuberculosis and Y. enterocolitica. Fragments of five housekeeping genes and a gene involved in the synthesis of lipopolysaccharide were sequenced from 36 strains representing the global diversity of Y. pestis and from 12-13 strains from each of the other species. No sequence diversity was found in any Y. pestis gene, and these alleles were identical or nearly identical to alleles from Y. pseudotuberculosis. Thus, Y. pestis is a clone that evolved from Y. pseudotuberculosis 1,500-20,000 years ago, shortly before the first known pandemics of human plague. Three biovars (Antiqua, Medievalis, and Orientalis) have been distinguished by microbiologists within the Y. pestis clone. These biovars form distinct branches of a phylogenetic tree based on restriction fragment length polymorphisms of the locations of the IS100 insertion element. These data are consistent with previous inferences that Antiqua caused a plague pandemic in the sixth century, Medievalis caused the Black Death and subsequent epidemics during the second pandemic wave, and Orientalis caused the current plague pandemic.
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              Microevolution and history of the plague bacillus, Yersinia pestis.

              The association of historical plague pandemics with Yersinia pestis remains controversial, partly because the evolutionary history of this largely monomorphic bacterium was unknown. The microevolution of Y. pestis was therefore investigated by three different multilocus molecular methods, targeting genomewide synonymous SNPs, variation in number of tandem repeats, and insertion of IS100 insertion elements. Eight populations were recognized by the three methods, and we propose an evolutionary tree for these populations, rooted on Yersinia pseudotuberculosis. The tree invokes microevolution over millennia, during which enzootic pestoides isolates evolved. This initial phase was followed by a binary split 6,500 years ago, which led to populations that are more frequently associated with human disease. These populations do not correspond directly to classical biovars that are based on phenotypic properties. Thus, we recommend that henceforth groupings should be based on molecular signatures. The age of Y. pestis inferred here is compatible with the dates of historical pandemic plague. However, it is premature to infer an association between any modern molecular grouping and a particular pandemic wave that occurred before the 20th century.
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                Author and article information

                Contributors
                Role: Editor
                Journal
                PLoS Pathog
                plos
                plospath
                PLoS Pathogens
                Public Library of Science (San Francisco, USA )
                1553-7366
                1553-7374
                October 2010
                October 2010
                7 October 2010
                : 6
                : 10
                : e1001134
                Affiliations
                [1 ]Institute for Anthropology, Johannes Gutenberg University, Mainz, Germany
                [2 ]Laboratory of Criminalistic Sciences Department of Anatomy, Pharmacology and Legal Medicine, University of Turin, Turin, Italy
                [3 ]Unité d'Anthropologie Bioculturelle, Faculté de Medecine, University of Mediterranean-CNRS-EFS, Marseille, France
                [4 ]Centre d'Études Préhistoire, Antiquité, Moyen-âge, UMR 6130 CNRS–250 University of Nice, Valbonne, France
                [5 ]Center for Plague, Institute Pasteur de Madagascar, World Health Organization Collaborating, Antananarivo, Madagascar
                [6 ]Department of Anatomy and Embryology Medical Faculty, Georg-August University, Göttingen, Germany
                [7 ]Inrap, Villeneuve-d'Ascq Archaeological Center, Villeneuve-d'Ascq, France
                [8 ]Laboratoire d'Anthropologie des Populations du Passé, Université Bordeaux 1, Talence, France
                [9 ]Department of Monuments and Archaeology, Municipality of Bergen op Zoom, Bergen op Zoom, The Netherlands
                [10 ]Barge's Anthropologica, Department of Anatomy and Embryology, Leiden University Medical Center, Leiden, The Netherlands
                [11 ]Division of Archaeological Sciences, University of Bradford, Bradford, West Yorkshire, United Kingdom
                [12 ]Department of Human Evolution, Max Planck Institute for Evolutionary Anthropology, Leipzig, Germany
                [13 ]Worcestershire Historic Environment and Archaeology Service, Worcestershire County Council, Worcester, United Kingdom
                [14 ]Environmental Research Institute, University College Cork, Cork, Ireland
                [15 ]Yersinia Research Unit, Institut Pasteur, Paris, France
                University of Notre Dame, United States of America
                Author notes

                Conceived the experiment: R. Bianucci, M. Schultz, B. Bramanti. Carried out aDNA research: S. Haensch, B. Bramanti. Performed the RDT analysis: R. Bianucci, M. Rajerison. Carried out the data analysis together with E. Carniel and M. Achtman: S. Haensch, B. Bramanti. Contributed with archaeological and historical data: M. Signoli, S. Kacki, M. Vermunt, D. Weston, D. Hurst. Wrote the paper: S. Haensch, M. Achtman, E. Carniel, B. Bramanti.

                Article
                10-PLPA-RA-3455R2
                10.1371/journal.ppat.1001134
                2951374
                20949072
                5ac1290a-75d4-4e0f-aa16-c2a844011788
                Haensch et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
                History
                : 28 May 2010
                : 7 September 2010
                Page count
                Pages: 8
                Categories
                Research Article
                Evolutionary Biology
                Evolutionary Biology/Human Evolution
                Genetics and Genomics
                Genetics and Genomics/Microbial Evolution and Genomics
                Infectious Diseases
                Infectious Diseases/Bacterial Infections
                Microbiology/Microbial Evolution and Genomics
                Molecular Biology/Molecular Evolution

                Infectious disease & Microbiology
                Infectious disease & Microbiology

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