A seventeenth-century Mycobacterium tuberculosis genome supports a Neolithic emergence of the Mycobacterium tuberculosis complex
Abstract Background Although tuberculosis accounts for the highest mortality from a bacterial infection on a global scale, questions persist regarding its origin. One hypothesis based on modern Mycobacterium tuberculosis complex (MTBC) genomes suggests their most recent common ancestor followed huma...
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doaj-10aeed7bf557409b90db23ff5640aa172020-11-25T03:35:51ZengBMCGenome Biology1474-760X2020-08-0121112410.1186/s13059-020-02112-1A seventeenth-century Mycobacterium tuberculosis genome supports a Neolithic emergence of the Mycobacterium tuberculosis complexSusanna Sabin0Alexander Herbig1Åshild J. Vågene2Torbjörn Ahlström3Gracijela Bozovic4Caroline Arcini5Denise Kühnert6Kirsten I. Bos7Department of Archaeogenetics, Max Planck Institute for the Science of Human HistoryDepartment of Archaeogenetics, Max Planck Institute for the Science of Human HistoryDepartment of Archaeogenetics, Max Planck Institute for the Science of Human HistoryDepartment of Archaeology and Ancient History, Lund UniversityDepartment of Medical Imaging and Clinical Physiology, Skåne University Hospital Lund and Lund UniversityArkeologerna, National Historical MuseumTransmission, Infection, Diversification & Evolution Group, Max Planck Institute for the Science of Human HistoryDepartment of Archaeogenetics, Max Planck Institute for the Science of Human HistoryAbstract Background Although tuberculosis accounts for the highest mortality from a bacterial infection on a global scale, questions persist regarding its origin. One hypothesis based on modern Mycobacterium tuberculosis complex (MTBC) genomes suggests their most recent common ancestor followed human migrations out of Africa approximately 70,000 years before present. However, studies using ancient genomes as calibration points have yielded much younger dates of less than 6000 years. Here, we aim to address this discrepancy through the analysis of the highest-coverage and highest-quality ancient MTBC genome available to date, reconstructed from a calcified lung nodule of Bishop Peder Winstrup of Lund (b. 1605–d. 1679). Results A metagenomic approach for taxonomic classification of whole DNA content permitted the identification of abundant DNA belonging to the human host and the MTBC, with few non-TB bacterial taxa comprising the background. Genomic enrichment enabled the reconstruction of a 141-fold coverage M. tuberculosis genome. In utilizing this high-quality, high-coverage seventeenth-century genome as a calibration point for dating the MTBC, we employed multiple Bayesian tree models, including birth-death models, which allowed us to model pathogen population dynamics and data sampling strategies more realistically than those based on the coalescent. Conclusions The results of our metagenomic analysis demonstrate the unique preservation environment calcified nodules provide for DNA. Importantly, we estimate a most recent common ancestor date for the MTBC of between 2190 and 4501 before present and for Lineage 4 of between 929 and 2084 before present using multiple models, confirming a Neolithic emergence for the MTBC.http://link.springer.com/article/10.1186/s13059-020-02112-1TuberculosisAncient DNAMycobacterium tuberculosisMolecular datingMetagenomics |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Susanna Sabin Alexander Herbig Åshild J. Vågene Torbjörn Ahlström Gracijela Bozovic Caroline Arcini Denise Kühnert Kirsten I. Bos |
spellingShingle |
Susanna Sabin Alexander Herbig Åshild J. Vågene Torbjörn Ahlström Gracijela Bozovic Caroline Arcini Denise Kühnert Kirsten I. Bos A seventeenth-century Mycobacterium tuberculosis genome supports a Neolithic emergence of the Mycobacterium tuberculosis complex Genome Biology Tuberculosis Ancient DNA Mycobacterium tuberculosis Molecular dating Metagenomics |
author_facet |
Susanna Sabin Alexander Herbig Åshild J. Vågene Torbjörn Ahlström Gracijela Bozovic Caroline Arcini Denise Kühnert Kirsten I. Bos |
author_sort |
Susanna Sabin |
title |
A seventeenth-century Mycobacterium tuberculosis genome supports a Neolithic emergence of the Mycobacterium tuberculosis complex |
title_short |
A seventeenth-century Mycobacterium tuberculosis genome supports a Neolithic emergence of the Mycobacterium tuberculosis complex |
title_full |
A seventeenth-century Mycobacterium tuberculosis genome supports a Neolithic emergence of the Mycobacterium tuberculosis complex |
title_fullStr |
A seventeenth-century Mycobacterium tuberculosis genome supports a Neolithic emergence of the Mycobacterium tuberculosis complex |
title_full_unstemmed |
A seventeenth-century Mycobacterium tuberculosis genome supports a Neolithic emergence of the Mycobacterium tuberculosis complex |
title_sort |
seventeenth-century mycobacterium tuberculosis genome supports a neolithic emergence of the mycobacterium tuberculosis complex |
publisher |
BMC |
series |
Genome Biology |
issn |
1474-760X |
publishDate |
2020-08-01 |
description |
Abstract Background Although tuberculosis accounts for the highest mortality from a bacterial infection on a global scale, questions persist regarding its origin. One hypothesis based on modern Mycobacterium tuberculosis complex (MTBC) genomes suggests their most recent common ancestor followed human migrations out of Africa approximately 70,000 years before present. However, studies using ancient genomes as calibration points have yielded much younger dates of less than 6000 years. Here, we aim to address this discrepancy through the analysis of the highest-coverage and highest-quality ancient MTBC genome available to date, reconstructed from a calcified lung nodule of Bishop Peder Winstrup of Lund (b. 1605–d. 1679). Results A metagenomic approach for taxonomic classification of whole DNA content permitted the identification of abundant DNA belonging to the human host and the MTBC, with few non-TB bacterial taxa comprising the background. Genomic enrichment enabled the reconstruction of a 141-fold coverage M. tuberculosis genome. In utilizing this high-quality, high-coverage seventeenth-century genome as a calibration point for dating the MTBC, we employed multiple Bayesian tree models, including birth-death models, which allowed us to model pathogen population dynamics and data sampling strategies more realistically than those based on the coalescent. Conclusions The results of our metagenomic analysis demonstrate the unique preservation environment calcified nodules provide for DNA. Importantly, we estimate a most recent common ancestor date for the MTBC of between 2190 and 4501 before present and for Lineage 4 of between 929 and 2084 before present using multiple models, confirming a Neolithic emergence for the MTBC. |
topic |
Tuberculosis Ancient DNA Mycobacterium tuberculosis Molecular dating Metagenomics |
url |
http://link.springer.com/article/10.1186/s13059-020-02112-1 |
work_keys_str_mv |
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