Phylogenomics and antimicrobial resistance of the leprosy bacillus Mycobacterium leprae
Benjak APapers in this archive, Avanzi CPapers in this archive, Singh PPapers in this archive, Loiseau CPapers in this archive, Girma SPapers in this archive, Busso PPapers in this archive, Fontes ANBPapers in this archive, Miyamoto YPapers in this archive, Namisato MPapers in this archive, Bobosha KPapers in this archive, Salgado CGPapers in this archive, da Silva MBPapers in this archive, Bouth RCPapers in this archive, Frade MACPapers in this archive, Filho FBPapers in this archive, Barreto JGPapers in this archive, Nery JACPapers in this archive, Bührer-Sékula SPapers in this archive, Lupien APapers in this archive, Al-Samie ARPapers in this archive, Al-Qubati YPapers in this archive, Alkubati ASPapers in this archive, Bretzel GPapers in this archive, Vera-Cabrera LPapers in this archive, Sakho FPapers in this archive, Johnson CRPapers in this archive, Kodio MPapers in this archive, Fomba APapers in this archive, Sow SOPapers in this archive, Gado MPapers in this archive, Konaté OPapers in this archive, Stefani MMAPapers in this archive, Penna GOPapers in this archive, Suffys PNPapers in this archive, Sarno ENPapers in this archive, Moraes MOPapers in this archive, Rosa PSPapers in this archive, Baptista IMFDPapers in this archive, Spencer JSPapers in this archive, Aseffa APapers in this archive, Matsuoka MPapers in this archive, Kai MPapers in this archive, Cole STPapers in this archive
Abstract
Leprosy is a chronic human disease caused by the yet-uncultured pathogen Mycobacterium leprae. Although readily curable with multidrug therapy (MDT), over 200,000 new cases are still reported annually. Here, we obtain M. leprae genome sequences from DNA extracted directly from patients’ skin biopsies using a customized protocol. Comparative and phylogenetic analysis of 154 genomes from 25 countries provides insight into evolution and antimicrobial resistance, uncovering lineages and phylogeographic trends, with the most ancestral strains linked to the Far East. In addition to known MDT-resistance mutations, we detect other mutations associated with antibiotic resistance, and retrace a potential stepwise emergence of extensive drug resistance in the pre-MDT era. Some of the previously undescribed mutations occur in genes that are apparently subject to positive selection, and two of these (ribD, fadD9) are restricted to drug-resistant strains. Finally, nonsense mutations in the nth excision repair gene are associated with greater sequence diversity and drug resistance.
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