TY - JOUR
T1 - Comparative genomics of Mycobacterium africanum Lineage 5 and Lineage 6 from Ghana suggests distinct ecological niches
AU - Otchere, Isaac Darko
AU - Coscollá, Mireia
AU - Sánchez-Busó, Leonor
AU - Asante-Poku, Adwoa
AU - Brites, Daniela
AU - Loiseau, Chloe
AU - Meehan, Conor
AU - Osei-Wusu, Stephen
AU - Forson, Audrey
AU - Laryea, Clement
AU - Yahayah, Abdallah Iddrisu
AU - Baddoo, Akosua
AU - Ansa, Gloria Akosua
AU - Aboagye, Samuel Yaw
AU - Asare, Prince
AU - Borrell, Sonia
AU - Gehre, Florian
AU - Beckert, Patrick
AU - Kohl, Thomas A.
AU - N’dira, Sanoussi
AU - Beisel, Christian
AU - Antonio, Martin
AU - Niemann, Stefan
AU - de Jong, Bouke C.
AU - Parkhill, Julian
AU - Harris, Simon R.
AU - Gagneux, Sebastien
AU - Yeboah-Manu, Dorothy
N1 - Publisher Copyright:
© 2018, The Author(s).
PY - 2018/12/1
Y1 - 2018/12/1
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=85050671725&partnerID=8YFLogxK
U2 - 10.1038/s41598-018-29620-2
DO - 10.1038/s41598-018-29620-2
M3 - Article
C2 - 30050166
AN - SCOPUS:85050671725
SN - 2045-2322
VL - 8
JO - Scientific Reports
JF - Scientific Reports
IS - 1
M1 - 11269
ER -