Insight into the evolution and origin of leprosy bacilli from the genome sequence of Mycobacterium lepromatosis.
- Singh P Global Health Institute, Ecole Polytechnique Fédérale de Lausanne, 1015 Lausanne, Switzerland;
- Benjak A Global Health Institute, Ecole Polytechnique Fédérale de Lausanne, 1015 Lausanne, Switzerland;
- Schuenemann VJ Institute for Archaeological Sciences, University of Tübingen, 72076 Tübingen, Germany;
- Herbig A Institute for Archaeological Sciences, University of Tübingen, 72076 Tübingen, Germany;
- Avanzi C Global Health Institute, Ecole Polytechnique Fédérale de Lausanne, 1015 Lausanne, Switzerland;
- Busso P Global Health Institute, Ecole Polytechnique Fédérale de Lausanne, 1015 Lausanne, Switzerland;
- Nieselt K Center for Bioinformatics Tübingen, University of Tübingen, 72070 Tübingen, Germany;
- Krause J Institute for Archaeological Sciences, University of Tübingen, 72076 Tübingen, Germany; Senckenberg Centre for Human Evolution and Palaeoenvironment, University of Tübingen, 72070 Tübingen, Germany; Max Planck Institute for the Science of Human History, 07745 Jena, Germany; and.
- Vera-Cabrera L Laboratorio Interdisciplinario de Investigación Dermatológica, Servicio de Dermatología, Hospital Universitario, Universidad Autónoma de Nuevo León, 64460 Monterrey, Nuevo León, Mexico.
- Cole ST Global Health Institute, Ecole Polytechnique Fédérale de Lausanne, 1015 Lausanne, Switzerland; stewart.cole@epfl.ch.
- 2015-04-02
Published in:
- Proceedings of the National Academy of Sciences of the United States of America. - 2015
Mycobacterium leprae
Mycobacterium lepromatosis
comparative genomics
genome sequencing
reductive evolution
Biopsy
Chromosome Mapping
Contig Mapping
DNA, Bacterial
Evolution, Molecular
Genome, Bacterial
Genomics
Geography
Humans
Leprosy
Mexico
Molecular Sequence Data
Mycobacterium
Phylogeny
Phylogeography
Polymerase Chain Reaction
Polymorphism, Single Nucleotide
Sequence Analysis, DNA
Species Specificity
English
Mycobacterium lepromatosis is an uncultured human pathogen associated with diffuse lepromatous leprosy and a reactional state known as Lucio's phenomenon. By using deep sequencing with and without DNA enrichment, we obtained the near-complete genome sequence of M. lepromatosis present in a skin biopsy from a Mexican patient, and compared it with that of Mycobacterium leprae, which has undergone extensive reductive evolution. The genomes display extensive synteny and are similar in size (∼3.27 Mb). Protein-coding genes share 93% nucleotide sequence identity, whereas pseudogenes are only 82% identical. The events that led to pseudogenization of 50% of the genome likely occurred before divergence from their most recent common ancestor (MRCA), and both M. lepromatosis and M. leprae have since accumulated new pseudogenes or acquired specific deletions. Functional comparisons suggest that M. lepromatosis has lost several enzymes required for amino acid synthesis whereas M. leprae has a defective heme pathway. M. lepromatosis has retained all functions required to infect the Schwann cells of the peripheral nervous system and therefore may also be neuropathogenic. A phylogeographic survey of 227 leprosy biopsies by differential PCR revealed that 221 contained M. leprae whereas only six, all from Mexico, harbored M. lepromatosis. Phylogenetic comparisons indicate that M. lepromatosis is closer than M. leprae to the MRCA, and a Bayesian dating analysis suggests that they diverged from their MRCA approximately 13.9 Mya. Thus, despite their ancient separation, the two leprosy bacilli are remarkably conserved and still cause similar pathologic conditions.
- Language
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- English
- Open access status
- bronze
- Identifiers
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- DOI 10.1073/pnas.1421504112
- PMID 25831531
- Persistent URL
- https://sonar.ch/global/documents/150984
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