Ben Krause-Kyora
University of Kiel
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Featured researches published by Ben Krause-Kyora.
Science | 2013
Verena J. Schuenemann; Pushpendra Singh; Thomas A. Mendum; Ben Krause-Kyora; Günter Jäger; Kirsten I. Bos; Alexander Herbig; Christos Economou; Andrej Benjak; Philippe Busso; Almut Nebel; Jesper Lier Boldsen; Anna Kjellström; Huihai Wu; Graham R. Stewart; G. Michael Taylor; Peter Bauer; Oona Y.-C. Lee; Houdini H.T. Wu; David E. Minnikin; Gurdyal S. Besra; Katie Tucker; Simon Roffey; Samba O. Sow; Stewart T. Cole; Kay Nieselt; Johannes Krause
Leprosy: Ancient and Modern In medieval Europe, leprosy was greatly feared: Sufferers had to wear bells and were shunned and kept isolated from society. Although leprosy largely disappeared from Europe in the 16th century, elsewhere in the world almost a quarter of a million cases are still reported annually, despite the availability of effective drugs. Schuenemann et al. (p. 179, published online 13 June; see the 14 June News story by Gibbons, p. 1278) probed the origins of leprosy bacilli by using a genomic capture-based approach on DNA obtained from skeletal remains from the 10th to 14th centuries. Because the unique mycolic acids of this mycobacterium protect its DNA, for one Danish sample over 100-fold, coverage of the genome was possible. Sequencing suggests a link between the middle-eastern and medieval European strains, which falls in line with social historical expectations that the returning expeditionary forces of antiquity originally spread the pathogen. Subsequently, Europeans took the bacterium westward to the Americas. Overall, ancient and modern strains remain remarkably similar, with no apparent loss of virulence genes, indicating it was most probably improvements in social conditions that led to leprosys demise in Europe. Five European individuals who lived during the Middle Ages provide a look backward at leprosy. Leprosy was endemic in Europe until the Middle Ages. Using DNA array capture, we have obtained genome sequences of Mycobacterium leprae from skeletons of five medieval leprosy cases from the United Kingdom, Sweden, and Denmark. In one case, the DNA was so well preserved that full de novo assembly of the ancient bacterial genome could be achieved through shotgun sequencing alone. The ancient M. leprae sequences were compared with those of 11 modern strains, representing diverse genotypes and geographic origins. The comparisons revealed remarkable genomic conservation during the past 1000 years, a European origin for leprosy in the Americas, and the presence of an M. leprae genotype in medieval Europe now commonly associated with the Middle East. The exceptional preservation of M. leprae biomarkers, both DNA and mycolic acids, in ancient skeletons has major implications for palaeomicrobiology and human pathogen evolution.
Science | 2016
Frank Maixner; Ben Krause-Kyora; Dmitrij Turaev; Alexander Herbig; Michael R. Hoopmann; Janice L. Hallows; Ulrike Kusebauch; Eduard Egarter Vigl; Peter Malfertheiner; Francis Mégraud; Niall O’Sullivan; Giovanna Cipollini; Valentina Coia; Marco Samadelli; Lars Engstrand; Bodo Linz; Robert L. Moritz; Rudolf Grimm; Johannes Krause; Almut Nebel; Yoshan Moodley; Thomas Rattei; Albert Zink
Stomach ache for a European mummy Five thousand years ago in the European Alps, a man was shot by an arrow, then clubbed to death. His body was subsequently mummified by ice until glacier retreat exhumed him in 1991. Subsequently, this ancient corpse has provided a trove of intriguing information about copper-age Europeans. Now, Maixner et al. have identified the human pathogen Helicobacter pylori within the mummys stomach contents. The strain the “Iceman” hosted appears to most closely resemble pathogenic Asian strains found today in Central and Southern Asia. Science, this issue p. 162 Mummified remains from the Alps reveal an unexpected history for a human pathogen. The stomach bacterium Helicobacter pylori is one of the most prevalent human pathogens. It has dispersed globally with its human host, resulting in a distinct phylogeographic pattern that can be used to reconstruct both recent and ancient human migrations. The extant European population of H. pylori is known to be a hybrid between Asian and African bacteria, but there exist different hypotheses about when and where the hybridization took place, reflecting the complex demographic history of Europeans. Here, we present a 5300-year-old H. pylori genome from a European Copper Age glacier mummy. The “Iceman” H. pylori is a nearly pure representative of the bacterial population of Asian origin that existed in Europe before hybridization, suggesting that the African population arrived in Europe within the past few thousand years.
Nature Communications | 2013
Ben Krause-Kyora; Cheryl A. Makarewicz; Allowen Evin; Linus Girdland Flink; Keith Dobney; Greger Larson; Stefan Schreiber; Claus von Carnap-Bornheim; Almut Nebel
Mesolithic populations throughout Europe used diverse resource exploitation strategies that focused heavily on collecting and hunting wild prey. Between 5500 and 4200 cal BC, agriculturalists migrated into northwestern Europe bringing a suite of Neolithic technologies including domesticated animals. Here we investigate to what extent Mesolithic Ertebølle communities in northern Germany had access to domestic pigs, possibly through contact with neighbouring Neolithic agricultural groups. We employ a multidisciplinary approach, applying sequencing of ancient mitochondrial and nuclear DNA (coat colour-coding gene MC1R) as well as traditional and geometric morphometric (molar size and shape) analyses in Sus specimens from 17 Neolithic and Ertebølle sites. Our data from 63 ancient pig specimens show that Ertebølle hunter-gatherers acquired domestic pigs of varying size and coat colour that had both Near Eastern and European mitochondrial DNA ancestry. Our results also reveal that domestic pigs were present in the region ~500 years earlier than previously demonstrated.
American Journal of Physical Anthropology | 2012
Esther J. Lee; Cheryl A. Makarewicz; Rebecca Renneberg; Melanie Harder; Ben Krause-Kyora; Stephanie Müller; Sven Ostritz; Lars Fehren-Schmitz; Stefan Schreiber; Johannes Müller; Nicole von Wurmb-Schwark; Almut Nebel
The transition from hunting and gathering to agriculture in Europe is associated with demographic changes that may have shifted the human gene pool of the region as a result of an influx of Neolithic farmers from the Near East. However, the genetic composition of populations after the earliest Neolithic, when a diverse mosaic of societies that had been fully engaged in agriculture for some time appeared in central Europe, is poorly known. At this period during the Late Neolithic (ca. 2,800-2,000 BC), regionally distinctive burial patterns associated with two different cultural groups emerge, Bell Beaker and Corded Ware, and may reflect differences in how these societies were organized. Ancient DNA analyses of human remains from the Late Neolithic Bell Beaker site of Kromsdorf, Germany showed distinct mitochondrial haplotypes for six individuals, which were classified under the haplogroups I1, K1, T1, U2, U5, and W5, and two males were identified as belonging to the Y haplogroup R1b. In contrast to other Late Neolithic societies in Europe emphasizing maintenance of biological relatedness in mortuary contexts, the diversity of maternal haplotypes evident at Kromsdorf suggests that burial practices of Bell Beaker communities operated outside of social norms based on shared maternal lineages. Furthermore, our data, along with those from previous studies, indicate that modern U5-lineages may have received little, if any, contribution from the Mesolithic or Neolithic mitochondrial gene pool.
World Archaeology | 2014
Allowen Evin; Linus Girdland Flink; Ben Krause-Kyora; Cheryl A. Makarewicz; Soenke Hartz; Stefan Schreiber; Nicole von Wurmb-Schwark; Almut Nebel; Claus von Carnap-Bornheim; Greger Larson; Keith Dobney
Abstract In their critique of our paper (Krause-Kyora et al. 2013), Rowley-Conwy and Zeder focus on two primary issues. Firstly, they discuss issues associated with the terminology and definitions of animal domestication. Secondly, they question the techniques we employed to explore it. While we completely agree with their points related to terminology, we feel they have misunderstood both the principals and application of shape analyses using geometric morphometrics, and that this misunderstanding undermines their criticism. Having said that, and though our differences are easily overstated, our respective interpretations of the data presented in Krause-Kyora et al. (2013) overlap significantly.
Nature Communications | 2017
Friederike Flachsbart; Janina Dose; Liljana Gentschew; Claudia Geismann; Amke Caliebe; Carolin Knecht; Marianne Nygaard; Nandini Badarinarayan; Abdou ElSharawy; Sandra May; Anne Luzius; Guillermo G. Torres; Marlene Jentzsch; Michael Forster; Robert Häsler; Kathrin Pallauf; Wolfgang Lieb; Céline Derbois; Pilar Galan; Dmitriy Drichel; Alexander Arlt; Andreas Till; Ben Krause-Kyora; Gerald Rimbach; Hélène Blanché; Jean-François Deleuze; Lene Christiansen; Kaare Christensen; Michael Nothnagel; Philip Rosenstiel
FOXO3 is consistently annotated as a human longevity gene. However, functional variants and underlying mechanisms for the association remain unknown. Here, we perform resequencing of the FOXO3 locus and single-nucleotide variant (SNV) genotyping in three European populations. We find two FOXO3 SNVs, rs12206094 and rs4946935, to be most significantly associated with longevity and further characterize them functionally. We experimentally validate the in silico predicted allele-dependent binding of transcription factors (CTCF, SRF) to the SNVs. Specifically, in luciferase reporter assays, the longevity alleles of both variants show considerable enhancer activities that are reversed by IGF-1 treatment. An eQTL database search reveals that the alleles are also associated with higher FOXO3 mRNA expression in various human tissues, which is in line with observations in long-lived model organisms. In summary, we present experimental evidence for a functional link between common intronic variants in FOXO3 and human longevity.FOXO3 is one of the few established longevity genes. Here, the authors fine-map the FOXO3-longevity association to two intronic SNPs and, using luciferase assays and EMSAs, show that these SNPs affect binding of transcription factors CTCF and SRF and associate with FOXO3 expression.
PLOS Pathogens | 2018
Verena J. Schuenemann; Charlotte Avanzi; Ben Krause-Kyora; Alexander Seitz; Alexander Herbig; Sarah Inskip; Marion Bonazzi; Ella Reiter; Christian Urban; Dorthe Dangvard Pedersen; G. Michael Taylor; Pushpendra Singh; Graham R. Stewart; Petr Velemínský; Jakub Likovsky; Antónia Marcsik; Erika Molnár; György Pálfi; Valentina Mariotti; Alessandro Riga; M. Giovanna Belcastro; Jesper Lier Boldsen; Almut Nebel; Simon Mays; Helen D. Donoghue; Sonia R. Zakrzewski; Andrej Benjak; Kay Nieselt; Stewart T. Cole; Johannes Krause
Studying ancient DNA allows us to retrace the evolutionary history of human pathogens, such as Mycobacterium leprae, the main causative agent of leprosy. Leprosy is one of the oldest recorded and most stigmatizing diseases in human history. The disease was prevalent in Europe until the 16th century and is still endemic in many countries with over 200,000 new cases reported annually. Previous worldwide studies on modern and European medieval M. leprae genomes revealed that they cluster into several distinct branches of which two were present in medieval Northwestern Europe. In this study, we analyzed 10 new medieval M. leprae genomes including the so far oldest M. leprae genome from one of the earliest known cases of leprosy in the United Kingdom—a skeleton from the Great Chesterford cemetery with a calibrated age of 415–545 C.E. This dataset provides a genetic time transect of M. leprae diversity in Europe over the past 1500 years. We find M. leprae strains from four distinct branches to be present in the Early Medieval Period, and strains from three different branches were detected within a single cemetery from the High Medieval Period. Altogether these findings suggest a higher genetic diversity of M. leprae strains in medieval Europe at various time points than previously assumed. The resulting more complex picture of the past phylogeography of leprosy in Europe impacts current phylogeographical models of M. leprae dissemination. It suggests alternative models for the past spread of leprosy such as a wide spread prevalence of strains from different branches in Eurasia already in Antiquity or maybe even an origin in Western Eurasia. Furthermore, these results highlight how studying ancient M. leprae strains improves understanding the history of leprosy worldwide.
eLife | 2018
Ben Krause-Kyora; Julian Susat; Felix M. Key; Denise Kühnert; Esther Bosse; Alexander Immel; Christoph Rinne; Sabin-Christin Kornell; Diego Yepes; Sören Franzenburg; Henrike O. Heyne; Thomas Meier; Sandra Lösch; Harald Meller; Susanne Friederich; Nicole Nicklisch; Kurt W. Alt; Stefan Schreiber; Andreas Tholey; Alexander Herbig; Almut Nebel; Johannes Krause
The hepatitis B virus (HBV) is one of the most widespread human pathogens known today, yet its origin and evolutionary history are still unclear and controversial. Here, we report the analysis of three ancient HBV genomes recovered from human skeletons found at three different archaeological sites in Germany. We reconstructed two Neolithic and one medieval HBV genome by de novo assembly from shotgun DNA sequencing data. Additionally, we observed HBV-specific peptides using paleo-proteomics. Our results demonstrated that HBV has circulated in the European population for at least 7000 years. The Neolithic HBV genomes show a high genomic similarity to each other. In a phylogenetic network, they do not group with any human-associated HBV genome and are most closely related to those infecting African non-human primates. The ancient viruses appear to represent distinct lineages that have no close relatives today and possibly went extinct. Our results reveal the great potential of ancient DNA from human skeletons in order to study the long-time evolution of blood borne viruses.
Nature Communications | 2018
Ben Krause-Kyora; Marcel Nutsua; Lisa Boehme; Federica Pierini; Dorthe Dangvard Pedersen; Sabin Kornell; Dmitriy Drichel; Marion Bonazzi; Lena Möbus; Peter Tarp; Julian Susat; Esther Bosse; Beatrix Willburger; Alexander H. Schmidt; Jürgen Sauter; Andre Franke; Michael Wittig; Amke Caliebe; Michael Nothnagel; Stefan Schreiber; Jesper Lier Boldsen; Tobias L. Lenz; Almut Nebel
Leprosy, a chronic infectious disease caused by Mycobacterium leprae (M. leprae), was very common in Europe till the 16th century. Here, we perform an ancient DNA study on medieval skeletons from Denmark that show lesions specific for lepromatous leprosy (LL). First, we test the remains for M. leprae DNA to confirm the infection status of the individuals and to assess the bacterial diversity. We assemble 10 complete M. leprae genomes that all differ from each other. Second, we evaluate whether the human leukocyte antigen allele DRB1*15:01, a strong LL susceptibility factor in modern populations, also predisposed medieval Europeans to the disease. The comparison of genotype data from 69 M. leprae DNA-positive LL cases with those from contemporary and medieval controls reveals a statistically significant association in both instances. In addition, we observe that DRB1*15:01 co-occurs with DQB1*06:02 on a haplotype that is a strong risk factor for inflammatory diseases today.Leprosy, caused by infection with Mycobacterium leprae, was common in Europe in the Middle Ages. Here, Krause-Kyora et al. analyze ancient DNA from a medieval Danish leprosarium to assemble 10 complete bacterial genomes and perform association analysis of the DRB1*15:01 allele with risk of leprosy infection.
Current Biology | 2018
Frank Maixner; Dmitrij Turaev; Amaury Cazenave-Gassiot; Marek Janko; Ben Krause-Kyora; Michael R. Hoopmann; Ulrike Kusebauch; Mark J. Sartain; Gea Guerriero; Niall O’Sullivan; Matthew D. Teasdale; Giovanna Cipollini; Alice Paladin; Valeria Mattiangeli; Marco Samadelli; Umberto Tecchiati; Andreas Putzer; Mine Palazoglu; John K. Meissen; Sandra Lösch; Philipp Rausch; John F. Baines; Bum Jin Kim; Hyun-Joo An; Paul Gostner; Eduard Egarter-Vigl; Peter Malfertheiner; Andreas Keller; Robert W. Stark; Markus R. Wenk
Summary The history of humankind is marked by the constant adoption of new dietary habits affecting human physiology, metabolism, and even the development of nutrition-related disorders. Despite clear archaeological evidence for the shift from hunter-gatherer lifestyle to agriculture in Neolithic Europe [1], very little information exists on the daily dietary habits of our ancestors. By undertaking a complementary -omics approach combined with microscopy, we analyzed the stomach content of the Iceman, a 5,300-year-old European glacier mummy [2, 3]. He seems to have had a remarkably high proportion of fat in his diet, supplemented with fresh or dried wild meat, cereals, and traces of toxic bracken. Our multipronged approach provides unprecedented analytical depth, deciphering the nutritional habit, meal composition, and food-processing methods of this Copper Age individual.