Comparative genomics of Mycobacterium africanum Lineage 5 and Lineage 6 from Ghana suggests different ecological niches
Isaac Darko OtchereiD, Mireia CoscolláiD, Leonor Sánchez-BusóiD, Adwoa Asante-PokuiD, Daniela BritesiD, Chloé LoiseauiD, Conor Joseph MeehaniD, Stephen Osei-WusuiD, Audrey G. ForsoniD, Clement LaryeaiD, Abdallah Iddrisu Yahayah, Akosua Baddoo, Gloria Akosua AnsaiD, Samuel Yaw AboagyeiD, Prince Philip Ankapong AsareiD, Sònia BorrelliD, Florian GehreiD, Patrick Beckert, Thomas Andreas KohliD, N'Dira SanoussiiD, Christian BeiseliD, Martín AntonioiD, Stefan NiemanniD, Bouke Catherine de JongiD, Julian ParkhilliD, , Dorothy Yeboah‐ManuiD
Abstract
Mycobacterium africanum (Maf) causes up to half of human tuberculosis in West Africa, but little is known on this pathogen. We compared the genomes of 253 Maf clinical isolates from Ghana, including both L5 and L6. We found that the genomic diversity of L6 was higher than in L5, and the selection pressures differed between both groups. Regulatory proteins appeared to evolve neutrally in L5 but under purifying selection in L6. Conversely, human T cell epitopes were under purifying selection in L5, but under positive selection in L6. Although only 10% of the T cell epitopes were variable, mutations were mostly lineage-specific. Our findings indicate that Maf L5 and L6 are genomically distinct, possibly reflecting different ecological niches.
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