# Whole-genome and pangenome insights into Mycobacterium colombiense clinical isolates from human infections

**Authors:** Chutinthorn Oungbamnet, Yothin Hinwan, Nut Nithimongkolchai, Vorthon Sawaswong, Suwalak Chitcharoen, Kiatichai Faksri, Auttawit Sirichoat

PMC · DOI: 10.7717/peerj.20716 · PeerJ · 2026-02-02

## TL;DR

This study analyzes the genomes of 12 Mycobacterium colombiense isolates to understand their genetic diversity, drug resistance, and virulence.

## Contribution

The study provides the first comprehensive genomic and drug resistance analysis of M. colombiense clinical isolates from Thailand.

## Key findings

- M. colombiense isolates showed high resistance to moxifloxacin and linezolid.
- Pangenome analysis revealed a closed structure with low genetic variability among isolates.
- Antibiotic resistance genes and virulence factors were identified, suggesting immune evasion potential.

## Abstract

Nontuberculous mycobacteria are opportunistic pathogens which cause infections in various tissues, with the Mycobacterium avium complex (MAC) being a major cause of pulmonary diseases. Among MAC members, Mycobacterium colombiense is a clinically significant species with recognized pathogenic potential; however, studies on its genomic structure and genetic diversity remain limited.

This study investigated the drug susceptibility profiles and performed whole-genome sequencing of 12 clinical M. colombiense isolates from the Clinical Microbiology Laboratory at Srinagarind Hospital, Khon Kaen University, Khon Kaen, Thailand.

Based on minimum inhibitory concentration values, moxifloxacin resistance was most prevalent (100%), followed by linezolid (90%), clarithromycin (30%), and amikacin (30%). The presence of antibiotic resistance genes and virulence factors, including ESX secretion systems and efflux pumps, highlights the bacterium’s potential for immune evasion and survival under stress. Single nucleotide polymorphism-based phylogenetic analysis revealed a close genetic relatedness between the isolates. Pangenome analysis of 16 M. colombiense genomes (12 newly sequenced and four publicly available) identified 7,771 gene clusters, comprising 4,468 core genes, 1,834 accessory genes, and 1,469 unique genes, supporting a closed pangenome structure and indicating evolutionary conservation and low genetic variability among isolates.

This study provides valuable insight into the genomic diversity, antimicrobial resistance profiles, and virulence potential of M. colombiense isolates. These findings enhance understanding of the pathogen and may inform clinical management, targeted diagnostic development, and therapeutic strategies.

## Linked entities

- **Chemicals:** moxifloxacin (PubChem CID 152946), linezolid (PubChem CID 3929), clarithromycin (PubChem CID 84029), amikacin (PubChem CID 37768)
- **Diseases:** pulmonary diseases (MONDO:0005275)
- **Species:** Mycobacterium colombiense (taxon 339268)

## Full-text entities

- **Diseases:** infections (MESH:D007239), pulmonary diseases (MESH:D008171)
- **Chemicals:** amikacin (MESH:D000583), clarithromycin (MESH:D017291), linezolid (MESH:D000069349), moxifloxacin (MESH:D000077266)
- **Species:** Mycobacterium colombiense (species) [taxon 339268], Mycobacterium avium complex sp. (species) [taxon 37162], Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12875251/full.md

## References

73 references — full list in the complete paper: https://tomesphere.com/paper/PMC12875251/full.md

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Source: https://tomesphere.com/paper/PMC12875251