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Comparative genomics of Mycobacterium africanum Lineage 5 and Lineage 6 from Ghana suggests distinct ecological niches

  • Isaac Darko Otchere
  • , Mireia Coscollá
  • , Leonor Sánchez-Busó
  • , Adwoa Asante-Poku
  • , Daniela Brites
  • , Chloe Loiseau
  • , Conor Meehan
  • , Stephen Osei-Wusu
  • , Audrey Forson
  • , Clement Laryea
  • , Abdallah Iddrisu Yahayah
  • , Akosua Baddoo
  • , Gloria Akosua Ansa
  • , Samuel Yaw Aboagye
  • , Prince Asare
  • , Sonia Borrell
  • , Florian Gehre
  • , Patrick Beckert
  • , Thomas A. Kohl
  • , Sanoussi N’dira
  • Christian Beisel, Martin Antonio, Stefan Niemann, Bouke C. de Jong, Julian Parkhill, Simon R. Harris, Sebastien Gagneux, Dorothy Yeboah-Manu
  • University of Ghana
  • Swiss Tropical and Public Health Institute Swiss TPH
  • University of Basel
  • University of Cambridge
  • Institute of Tropical Medicine Antwerp
  • Korle Bu Teaching Hospital
  • 37 Military Hospital
  • Tamale Teaching Hospital
  • London School of Hygiene & Tropical Medicine
  • Research Center Borstel - Leibniz Lung Center
  • German Center for Infection Research, Partner Site Hamburg-Borstel
  • National Reference Laboratory for Mycobacteria
  • Swiss Federal Institute of Technology Zurich
  • Warwick Medical School

Research output: Contribution to journalArticlepeer-review

38 Citations (Scopus)

Abstract

Mycobacterium africanum (Maf) causes a substantial proportion of human tuberculosis in some countries of West Africa, but little is known on this pathogen. We compared the genomes of 253 Maf clinical isolates from Ghana, including N = 175 Lineage 5 (L5) and N = 78 Lineage 6 (L6). We found that the genomic diversity of L6 was higher than in L5 despite the smaller sample size. Regulatory proteins appeared to evolve neutrally in L5 but under purifying selection in L6. Even though over 90% of the human T cell epitopes were conserved in both lineages, L6 showed a higher ratio of non-synonymous to synonymous single nucleotide variation in these epitopes overall compared to L5. Of the 10% human T cell epitopes that were variable, most carried mutations that were lineage-specific. Our findings indicate that Maf L5 and L6 differ in some of their population genomic characteristics, possibly reflecting different selection pressures linked to distinct ecological niches.

Original languageEnglish
Article number11269
JournalScientific Reports
Volume8
Issue number1
DOIs
Publication statusPublished - 1 Dec 2018

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

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