Onset of infectiousness explains differences in transmissibility across Mycobacterium tuberculosis lineages

Mycobacterium tuberculosis complex (MTBC) lineages show substantial variability in virulence, but the epidemiological consequences of this variability have not been studied in detail. Here, we aimed for a lineage-specific epidemiological characterization by applying phylodynamic models to genomic data from different countries, representing the most abundant MTBC lineages. Our results suggest that all lineages are associated with similar durations and levels of infectiousness, resulting in similar reproductive numbers. However, L1 and L6 are associated with a delayed onset of infectiousness, leading to longer periods between subsequent transmission events. Together, our findings highlight the role of MTBC genetic diversity in tuberculosis disease progression and transmission.

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Publication Details

Journal
Epidemics
Published
2025-03-12
DOI
https://doi.org/10.1016/j.epidem.2025.100821
Citations
3
Primary Topic
Tuberculosis Research and Epidemiology
Type
article
Field-Weighted Citation Impact
4.19

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article

Onset of infectiousness explains differences in transmissibility across Mycobacterium tuberculosis lineages

Cecilia Valenzuela Agüí, Etthel M. Windels, Daniela Brites, Bouke C. de Jong et al.
3 citations
Epidemics
Tuberculosis Research and Epidemiology
4.19
article

Onset of infectiousness explains differences in transmissibility across Mycobacterium tuberculosis lineages

Cecilia Valenzuela Agüí, Etthel M. Windels, Daniela Brites, Bouke C. de Jong, Conor Joseph Meehan, Tanja Stadler, Sònia Borrell, Galo Adrián Goig, Chloé Loiseau, Sébastien Gagneux, Michaela Zwyer
article en
3 citations

Abstract

Mycobacterium tuberculosis complex (MTBC) lineages show substantial variability in virulence, but the epidemiological consequences of this variability have not been studied in detail. Here, we aimed for a lineage-specific epidemiological characterization by applying phylodynamic models to genomic data from different countries, representing the most abundant MTBC lineages. Our results suggest that all lineages are associated with similar durations and levels of infectiousness, resulting in similar reproductive numbers. However, L1 and L6 are associated with a delayed onset of infectiousness, leading to longer periods between subsequent transmission events. Together, our findings highlight the role of MTBC genetic diversity in tuberculosis disease progression and transmission.

EpidemicsVol. 51
SIB Swiss Institute of Bioinformatics (CH), Swiss Tropical and Public Health Institute (CH), University of Basel (CH), Nottingham Trent University (GB), Instituut voor Tropische Geneeskunde (BE)
National Science Foundation, Universität Basel, European Commission, Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung, Eidgenössische Technische Hochschule Zürich, HORIZON EUROPE European Research Council
Openalex Percentile: Top 7%
Tuberculosis Research and Epidemiology
4.19
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