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

Author:

Coscolla Mireia1ORCID,Gagneux Sebastien23ORCID,Menardo Fabrizio23ORCID,Loiseau Chloé23ORCID,Ruiz-Rodriguez Paula1ORCID,Borrell Sonia23,Otchere Isaac Darko4ORCID,Asante-Poku Adwoa4ORCID,Asare Prince4ORCID,Sánchez-Busó Leonor56ORCID,Gehre Florian78,Sanoussi C. N’Dira910,Antonio Martin11,Affolabi Dissou10,Fyfe Janet12,Beckert Patrick1314,Niemann Stefan1314,Alabi Abraham S.15,Grobusch Martin P.161715ORCID,Kobbe Robin18ORCID,Parkhill Julian19,Beisel Christian20,Fenner Lukas21ORCID,Böttger Erik C.22ORCID,Meehan Conor J.23ORCID,Harris Simon R.245ORCID,de Jong Bouke C.9,Yeboah-Manu Dorothy4ORCID,Brites Daniela23ORCID

Affiliation:

1. I2SysBio, University of Valencia-FISABIO Joint Unit, Valencia, Spain

2. University of Basel, Basel, Switzerland

3. Swiss Tropical and Public Health Institute, Basel, Switzerland

4. Noguchi Memorial Institute for Medical Research, University of Ghana, Legon, Accra, Ghana

5. Wellcome Sanger Institute, Wellcome Genome Campus, Cambridge, UK

6. Centre for Genomic Pathogen Surveillance, Big Data Institute, Nuffield Department of Medicine, University of Oxford, Oxford, UK

7. Health Department, East African Community (EAC), Arusha, Tanzania

8. Infectious Disease Epidemiology Department, Bernhard-Nocht-Institute for Tropical Medicine, Hamburg, Germany

9. Mycobacteriology Unit, Institute of Tropical Medicine, Antwerp, Belgium

10. Laboratoire de Référence des Mycobactéries, Ministry of Health, Cotonou, Bénin

11. London School of Hygiene and Tropical Medicine, London, UK

12. Mycobacterium Reference Laboratory, Victoria Infectious Diseases Reference Laboratory, Peter Doherty Institute, Melbourne, Victoria, Australia

13. Partner Site Hamburg-Lübeck-Borstel-Riems, German Center for Infection Research, Borstel, Germany

14. Molecular and Experimental Mycobacteriology, Research Center Borstel, Borstel, Germany

15. Centre de Recherches Médicales en Lambaréné (Cermel), Lambaréné, Gabon

16. Center of Tropical Medicine and Travel Medicine, Department of Infectious Diseases, Amsterdam University Medical Centers, Amsterdam Infection and Immunity, Amsterdam Public Health, University of Amsterdam, Amsterdam, The Netherlands

17. Institut für Tropenmedizin, Deutsches Zentrum fuer Infektionsforschung, University of Tübingen, Tübingen, Germany

18. First Department of Medicine, Division of Infectious Diseases, University Medical Center Hamburg-Eppendorf, Germany

19. Department of Veterinary Medicine, University of Cambridge, Madingley Road, Cambridge, UK

20. Department of Biosystems Science and Engineering, ETH Zürich, Basel, Switzerland

21. Institute of Social and Preventive Medicine, University of Bern, Bern, Switzerland

22. Institute of Medical Microbiology, University of Zürich, Zürich, Switzerland

23. School of Chemistry and Biosciences, University of Bradford, Bradford, UK

24. Microbiotica Limited, Bioinnovation Centre, Wellcome Genome Campus, Cambridge, CB10 1DR, UK

Abstract

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.

Funder

Wellcome Trust

Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung

Ministerio de Ciencia, Innovación y Universidades

Conselleria d'Educació, Investigació, Cultura i Esport

European Society of Clinical Microbiology and Infectious Diseases

H2020 European Research Council

Publisher

Microbiology Society

Subject

General Medicine

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