Eighteenth-century genomes show that mixed infections were common at time of peak tuberculosis in Europe
Tuberculosis (TB) was once a major killer in Europe, but it is unclear how the strains and patterns of infection at ‘peak TB’ relate to what we see today. Here we describe 14 genome sequences of M. tuberculosis , representing 12 distinct genotypes, obtained from human remains from eighteenth-century...
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| Vydáno v: | Nature communications Ročník 6; číslo 1; s. 6717 |
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| Jazyk: | angličtina |
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07.04.2015
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| ISSN: | 2041-1723, 2041-1723 |
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| Abstract | Tuberculosis (TB) was once a major killer in Europe, but it is unclear how the strains and patterns of infection at ‘peak TB’ relate to what we see today. Here we describe 14 genome sequences of
M. tuberculosis
, representing 12 distinct genotypes, obtained from human remains from eighteenth-century Hungary using metagenomics. All our historic genotypes belong to
M. tuberculosis
Lineage 4. Bayesian phylogenetic dating, based on samples with well-documented dates, places the most recent common ancestor of this lineage in the late Roman period. We find that most bodies yielded more than one
M. tuberculosis
genotype and we document an intimate epidemiological link between infections in two long-dead individuals. Our results suggest that metagenomic approaches usefully inform detection and characterization of historical and contemporary infections.
Tuberculosis was once a major killer in Europe. Here the authors use metagenomics to obtain genomic sequences of
Mycobacterium tuberculosis
from human remains from eighteenth-century Hungary, revealing mixed infections within individuals as well as presence of the same strain in two individuals. |
|---|---|
| AbstractList | Tuberculosis (TB) was once a major killer in Europe, but it is unclear how the strains and patterns of infection at ‘peak TB' relate to what we see today. Here we describe 14 genome sequences of M. tuberculosis, representing 12 distinct genotypes, obtained from human remains from eighteenth-century Hungary using metagenomics. All our historic genotypes belong to M. tuberculosis Lineage 4. Bayesian phylogenetic dating, based on samples with well-documented dates, places the most recent common ancestor of this lineage in the late Roman period. We find that most bodies yielded more than one M. tuberculosis genotype and we document an intimate epidemiological link between infections in two long-dead individuals. Our results suggest that metagenomic approaches usefully inform detection and characterization of historical and contemporary infections.
Tuberculosis was once a major killer in Europe. Here the authors use metagenomics to obtain genomic sequences of Mycobacterium tuberculosis from human remains from eighteenth-century Hungary, revealing mixed infections within individuals as well as presence of the same strain in two individuals. Tuberculosis (TB) was once a major killer in Europe, but it is unclear how the strains and patterns of infection at ‘peak TB’ relate to what we see today. Here we describe 14 genome sequences of M. tuberculosis , representing 12 distinct genotypes, obtained from human remains from eighteenth-century Hungary using metagenomics. All our historic genotypes belong to M. tuberculosis Lineage 4. Bayesian phylogenetic dating, based on samples with well-documented dates, places the most recent common ancestor of this lineage in the late Roman period. We find that most bodies yielded more than one M. tuberculosis genotype and we document an intimate epidemiological link between infections in two long-dead individuals. Our results suggest that metagenomic approaches usefully inform detection and characterization of historical and contemporary infections. Tuberculosis (TB) was once a major killer in Europe, but it is unclear how the strains and patterns of infection at 'peak TB' relate to what we see today. Here we describe 14 genome sequences of M. tuberculosis, representing 12 distinct genotypes, obtained from human remains from eighteenth-century Hungary using metagenomics. All our historic genotypes belong to M. tuberculosis Lineage 4. Bayesian phylogenetic dating, based on samples with well-documented dates, places the most recent common ancestor of this lineage in the late Roman period. We find that most bodies yielded more than one M. tuberculosis genotype and we document an intimate epidemiological link between infections in two long-dead individuals. Our results suggest that metagenomic approaches usefully inform detection and characterization of historical and contemporary infections. Tuberculosis (TB) was once a major killer in Europe, but it is unclear how the strains and patterns of infection at ‘peak TB’ relate to what we see today. Here we describe 14 genome sequences of M. tuberculosis , representing 12 distinct genotypes, obtained from human remains from eighteenth-century Hungary using metagenomics. All our historic genotypes belong to M. tuberculosis Lineage 4. Bayesian phylogenetic dating, based on samples with well-documented dates, places the most recent common ancestor of this lineage in the late Roman period. We find that most bodies yielded more than one M. tuberculosis genotype and we document an intimate epidemiological link between infections in two long-dead individuals. Our results suggest that metagenomic approaches usefully inform detection and characterization of historical and contemporary infections. Tuberculosis was once a major killer in Europe. Here the authors use metagenomics to obtain genomic sequences of Mycobacterium tuberculosis from human remains from eighteenth-century Hungary, revealing mixed infections within individuals as well as presence of the same strain in two individuals. |
| ArticleNumber | 6717 |
| Author | Quick, Joshua Spigelman, Mark Szikossy, Ildikó Pap, Ildikó Achtman, Mark Pallen, Mark J. Loman, Nicholas J. Zhou, Zhemin Sergeant, Martin J. Millard, Andrew Kay, Gemma L. Donoghue, Helen D. Chan, Jacqueline Z.-M. |
| Author_xml | – sequence: 1 givenname: Gemma L. surname: Kay fullname: Kay, Gemma L. organization: Division of Translational and Systems Medicine, Microbiology and Infection Unit, Warwick Medical School, University of Warwick, Gibbet Hill Road – sequence: 2 givenname: Martin J. surname: Sergeant fullname: Sergeant, Martin J. organization: Division of Translational and Systems Medicine, Microbiology and Infection Unit, Warwick Medical School, University of Warwick, Gibbet Hill Road – sequence: 3 givenname: Zhemin surname: Zhou fullname: Zhou, Zhemin organization: Division of Translational and Systems Medicine, Microbiology and Infection Unit, Warwick Medical School, University of Warwick, Gibbet Hill Road – sequence: 4 givenname: Jacqueline Z.-M. surname: Chan fullname: Chan, Jacqueline Z.-M. organization: Division of Translational and Systems Medicine, Microbiology and Infection Unit, Warwick Medical School, University of Warwick, Gibbet Hill Road – sequence: 5 givenname: Andrew surname: Millard fullname: Millard, Andrew organization: Division of Translational and Systems Medicine, Microbiology and Infection Unit, Warwick Medical School, University of Warwick, Gibbet Hill Road – sequence: 6 givenname: Joshua surname: Quick fullname: Quick, Joshua organization: Institute of Microbiology and Infection, School of Biosciences, University of Birmingham – sequence: 7 givenname: Ildikó surname: Szikossy fullname: Szikossy, Ildikó organization: Department of Anthropology, Hungarian Natural History Museum, Ludovika tér 2–6 – sequence: 8 givenname: Ildikó surname: Pap fullname: Pap, Ildikó organization: Department of Anthropology, Hungarian Natural History Museum, Ludovika tér 2–6 – sequence: 9 givenname: Mark surname: Spigelman fullname: Spigelman, Mark organization: Department of Anatomy and Anthropology, Sackler Faculty of Medicine, Tel-Aviv University, Division of Infection and Immunity, Centre for Clinical Microbiology, University College London – sequence: 10 givenname: Nicholas J. surname: Loman fullname: Loman, Nicholas J. organization: Institute of Microbiology and Infection, School of Biosciences, University of Birmingham – sequence: 11 givenname: Mark surname: Achtman fullname: Achtman, Mark organization: Division of Translational and Systems Medicine, Microbiology and Infection Unit, Warwick Medical School, University of Warwick, Gibbet Hill Road – sequence: 12 givenname: Helen D. surname: Donoghue fullname: Donoghue, Helen D. organization: Division of Infection and Immunity, Centre for Clinical Microbiology, University College London – sequence: 13 givenname: Mark J. surname: Pallen fullname: Pallen, Mark J. email: m.pallen@warwick.ac.uk organization: Division of Translational and Systems Medicine, Microbiology and Infection Unit, Warwick Medical School, University of Warwick, Gibbet Hill Road |
| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/25848958$$D View this record in MEDLINE/PubMed |
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| Snippet | Tuberculosis (TB) was once a major killer in Europe, but it is unclear how the strains and patterns of infection at ‘peak TB’ relate to what we see today. Here... Tuberculosis (TB) was once a major killer in Europe, but it is unclear how the strains and patterns of infection at 'peak TB' relate to what we see today. Here... Tuberculosis (TB) was once a major killer in Europe, but it is unclear how the strains and patterns of infection at ‘peak TB' relate to what we see today. Here... |
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| Title | Eighteenth-century genomes show that mixed infections were common at time of peak tuberculosis in Europe |
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