• Sònia Borrell
  • Andrej Trauner
  • Daniela Brites
  • Leen Rigouts
  • Chloe Loiseau
  • Mireia Coscolla
  • Stefan Niemann
  • Bouke De Jong
  • Dorothy Yeboah-Manu
  • Midori Kato-Maeda
  • Julia Feldmann
  • Miriam Reinhard
  • Christian Beisel
  • Sebastien Gagneux

The Mycobacterium tuberculosis complex (MTBC) causes tuberculosis (TB) in humans and various other mammals. The human-adapted members of the MTBC comprise seven phylogenetic lineages that differ in their geographical distribution. There is growing evidence that this phylogeographic diversity modulates the outcome of TB infection and disease. For decades, TB research and development has focused on the two canonical MTBC laboratory strains H37Rv and Erdman, both of which belong to Lineage 4. Relying on only a few laboratory-adapted strains can be misleading as study results might not be directly transferrable to clinical settings where patients are infected with a diverse array of strains, including drug-resistant variants. Here, we argue for the need to expand TB research and development by incorporating the phylogenetic diversity of the MTBC. To facilitate such work, we have assembled a group of 20 genetically well-characterized clinical strains representing the seven known human-adapted MTBC lineages. With the "MTBC clinical strains reference set" we aim to provide a standardized resource for the TB community. We hope it will enable more direct comparisons between studies that explore the physiology of MTBC beyond the laboratory strains used thus far. We anticipate that detailed phenotypic analyses of this reference strain set will increase our understanding of TB biology and assist in the development of new control tools that are broadly effective.

Original languageEnglish
JournalPLoS ONE
Volume14
Issue number3
Pages (from-to)e0214088
ISSN1932-6203
DOIs
Publication statusPublished - 2019

Bibliographical note

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