A sister lineage of the Mycobacterium tuberculosis complex discovered in the African Great Lakes region

Jean Claude Semuto Ngabonziza(University of Antwerp), Chloé Loiseau(Swiss Tropical and Public Health Institute), Michaël Marceau(Centre National de la Recherche Scientifique), Agathe Jouet(Institut Pasteur de Lille), Fabrizio Menardo(Swiss Tropical and Public Health Institute), Oren Tzfadia(Instituut voor Tropische Geneeskunde), Rudy Antoine(Centre National de la Recherche Scientifique), Esdras Belamo Niyigena(Rwanda Biomedical Center), Wim Mulders(Instituut voor Tropische Geneeskunde), K. Fissette(Instituut voor Tropische Geneeskunde), Maren Diels(Instituut voor Tropische Geneeskunde), Cyril Gaudin(Institut Pasteur de Lille), Stéphanie Duthoy(Institut Pasteur de Lille), Willy Ssengooba(Makerere University), Emmanuel André(KU Leuven), Michel Kaswa(Programme National Multisectoriel de Lutte contre le sida), Yves Mucyo Habimana(Rwanda Biomedical Center), Daniela Brites(Swiss Tropical and Public Health Institute), Dissou Affolabi(Aidjan-Lagos Corridor Organization), Jean Baptiste Mazarati(Rwanda Biomedical Center), Bouke C. de Jong(Instituut voor Tropische Geneeskunde), Leen Rigouts(University of Antwerp), Sébastien Gagneux(Swiss Tropical and Public Health Institute), Conor J. Meehan(University of Bradford), Philip Supply(Centre National de la Recherche Scientifique)
Nature Communications
June 9, 2020
Cited by 221Open Access
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Abstract

The human- and animal-adapted lineages of the Mycobacterium tuberculosis complex (MTBC) are thought to have expanded from a common progenitor in Africa. However, the molecular events that accompanied this emergence remain largely unknown. Here, we describe two MTBC strains isolated from patients with multidrug resistant tuberculosis, representing an as-yet-unknown lineage, named Lineage 8 (L8), seemingly restricted to the African Great Lakes region. Using genome-based phylogenetic reconstruction, we show that L8 is a sister clade to the known MTBC lineages. Comparison with other complete mycobacterial genomes indicate that the divergence of L8 preceded the loss of the cobF genome region - involved in the cobalamin/vitamin B12 synthesis - and gene interruptions in a subsequent common ancestor shared by all other known MTBC lineages. This discovery further supports an East African origin for the MTBC and provides additional molecular clues on the ancestral genome reduction associated with adaptation to a pathogenic lifestyle.


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