# Genome-wide analyses of Mycobacterium tuberculosis complex isolates reveal insights into circulating lineages and drug resistance mutations in The Gambia

**Authors:** Leopold Tientcheu, Fatou Faal, Naffie Top, Olimatou Jobe, Sang Marie Colley, Abigail Ayorinde, Alieu Mendy, Binta Sarr-Kuyateh, Simon Donkor, Martin Antonio, Bouke de Jong, Andrea Rachow, Beate Kampmann, Jayne S. Sutherland, Hongwei Li, Tom Blundell, Susana Campino, Thomas Kohl, Viola Dreyer, Stefan Niemann, Arun Pandurangan, Taane Clark, Jody Phelan

PMC · DOI: 10.21203/rs.3.rs-5913893/v1 · Research Square · 2025-02-27

## TL;DR

This study uses genome sequencing to analyze TB strains in The Gambia, revealing lineage diversity and drug resistance patterns to improve local TB control.

## Contribution

The study provides new insights into MTBC lineage distribution and drug resistance mutations specific to The Gambia.

## Key findings

- Lineage 4 and 6 strains dominate in The Gambia, with lineage 4 showing higher genetic variability.
- A significant proportion of isolates had uncertain drug resistance mutations, including a lineage 6-specific ethambutol mutation.
- Drug resistance mutations often occur in conserved, solvent-inaccessible protein regions, affecting stability and fitness.

## Abstract

Tuberculosis (TB), caused by the Mycobacterium tuberculosis complex (MTBC), remains a pressing global health challenge, with the West African region, including The Gambia, experiencing a substantial burden. This study explores the genetic diversity of MTBC strains circulating in The Gambia for nearly two decades (2002–2021) to enhance understanding of drug resistance dynamics and inform targeted diagnostic and treatment strategies. Using whole-genome sequencing (WGS) data from 1,803 TB isolates, we identified the predominance of lineage 4 (L4, 67.2%) and lineage 6 (L6, 26.6%) strains, with L4 showing more significant genetic variability over time. Drug susceptibility analysis of these isolates revealed that 78% (1421 isolates) were drug-susceptible, while 6.5% (119 isolates) exhibited resistance, primarily to isoniazid, rifampicin, and their combination. Additionally, 15.5% (282 isolates) were classified as Other, having potential drug-resistance mutations of uncertain significance by the WHO catalogue. Interestingly, our resistance-associated analysis showed the lineage 6 specific ethambutol uncertain significance (by WHO catalogue) mutation (embC Ala307Thr) more prevalent in The Gambia than in West Africa and globally. Structural analysis showed that first-line drug resistance mutations frequently occur in solvent-inaccessible and conserved regions of proteins, often impacting protein stability and reflecting a balance between resistance, fitness, and evolutionary adaptation.

This study highlights the coexistence of globally prevalent and regionally restricted MTBC lineages, underscoring the importance of region-specific TB control measures. Integrating bioinformatic and structural analyses revealed many uncertain significant mutations by the WHO catalogue in The Gambian isolates compared to West Africa and globally. These findings reinforce the necessity of continuous genomic surveillance to address the evolving challenges of TB in high-burden settings like West Africa.

## Linked entities

- **Chemicals:** isoniazid (PubChem CID 3767), rifampicin (PubChem CID 135398735), ethambutol (PubChem CID 14052)
- **Diseases:** tuberculosis (MONDO:0018076), TB (MONDO:0018076)
- **Species:** Mycobacterium tuberculosis complex (taxon 77643)

## Full-text entities

- **Diseases:** TB (MESH:D014376)
- **Chemicals:** ethambutol (MESH:D004977), rifampicin (MESH:D012293), isoniazid (MESH:D007538)
- **Species:** Mycobacterium tuberculosis complex (species group) [taxon 77643]
- **Mutations:** Ala307Thr

## Full text

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## Figures

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## References

41 references — full list in the complete paper: https://tomesphere.com/paper/PMC11888536/full.md

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Source: https://tomesphere.com/paper/PMC11888536