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  3. Phylogenomics of Mycobacterium africanum reveals a new lineage and a complex evolutionary history.
 

Phylogenomics of Mycobacterium africanum reveals a new lineage and a complex evolutionary history.

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BORIS DOI
10.48350/152081
Date of Publication
February 2021
Publication Type
Article
Division/Institute

Institut für Sozial- ...

Author
Coscolla, Mireia
Gagneux, Sebastien
Menardo, Fabrizio
Loiseau, Chloé
Ruiz-Rodriguez, Paula
Borrell, Sonia
Otchere, Isaac Darko
Asante-Poku, Adwoa
Asare, Prince
Sánchez-Busó, Leonor
Gehre, Florian
Sanoussi, C N'Dira
Antonio, Martin
Affolabi, Dissou
Fyfe, Janet
Beckert, Patrick
Niemann, Stefan
Alabi, Abraham S
Grobusch, Martin P
Kobbe, Robin
Parkhill, Julian
Beisel, Christian
Fenner, Lukasorcid-logo
Institut für Sozial- und Präventivmedizin (ISPM)
Böttger, Erik C
Meehan, Conor J
Harris, Simon R
de Jong, Bouke C
Yeboah-Manu, Dorothy
Brites, Daniela
Subject(s)

600 - Technology::610...

300 - Social sciences...

Series
Microbial genomics
ISSN or ISBN (if monograph)
2057-5858
Publisher
Microbiology Society
Language
English
Publisher DOI
10.1099/mgen.0.000477
PubMed ID
33555243
Uncontrolled Keywords

Mycobacterium african...

Description
Human tuberculosis (TB) is caused by members of the Mycobacterium tuberculosis complex (MTBC). The MTBC comprises several human-adapted lineages known as M. tuberculosis sensu stricto, as well as two lineages (L5 and L6) traditionally referred to as Mycobacterium africanum. Strains of L5 and L6 are largely limited to West Africa for reasons unknown, and little is known of their genomic diversity, phylogeography and evolution. Here, we analysed the genomes of 350 L5 and 320 L6 strains, isolated from patients from 21 African countries, plus 5 related genomes that had not been classified into any of the known MTBC lineages. Our population genomic and phylogeographical analyses showed that the unclassified genomes belonged to a new group that we propose to name MTBC lineage 9 (L9). While the most likely ancestral distribution of L9 was predicted to be East Africa, the most likely ancestral distribution for both L5 and L6 was the Eastern part of West Africa. Moreover, we found important differences between L5 and L6 strains with respect to their phylogeographical substructure and genetic diversity. Finally, we could not confirm the previous association of drug-resistance markers with lineage and sublineages. Instead, our results indicate that the association of drug resistance with lineage is most likely driven by sample bias or geography. In conclusion, our study sheds new light onto the genomic diversity and evolutionary history of M. africanum, and highlights the need to consider the particularities of each MTBC lineage for understanding the ecology and epidemiology of TB in Africa and globally.
Handle
https://boris-portal.unibe.ch/handle/20.500.12422/40006
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Coscolla_MicrobGenom_2021.pdfAdobe PDF2.15 MBAttribution (CC BY 4.0)publishedOpen
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