# Resistance phenotypes and genomic features of Mycobacterium seoulense isolates

**Authors:** Jin Zhao, Xinli Shen, Lulu Jin, Songjun Ji, Xinling Pan

PMC · DOI: 10.3389/fcimb.2025.1553591 · Frontiers in Cellular and Infection Microbiology · 2025-04-07

## TL;DR

This study examines the antibiotic resistance and genetic diversity of Mycobacterium seoulense, an emerging pathogen, to better understand its clinical implications.

## Contribution

The study provides the first detailed analysis of drug resistance and genomic features of clinical M. seoulense isolates.

## Key findings

- All isolates showed high resistance to minocycline, doxycycline, and amikacin.
- Genomic diversity was observed, with 315 unique genes and two potential virulence genes identified.
- M. seoulense isolates demonstrated the ability to survive within macrophages.

## Abstract

Mycobacterium seoulense (M. seoulense) is an emerging pathogen increasingly associated with infections; however, its resistance phenotypes and genomic characteristics remain largely unknown.

Seven M. seoulense isolates were collected from clinical samples. Drug susceptibility testing was conducted using Sensititre™ SLOMYCO2 susceptibility plates. Whole genome sequencing and supporting bioinformatics analyses were performed to analyze the genomic features.

All M. seoulense isolates (n=7) exhibited growth on 7H10 agar medium containing thiophenecarboxylic acid hydrazide or p-Nitrobenzoic acid, with marked diversity in growth rates in liquid culture. All strains exhibited high minimum inhibitor concentrations (MICs) for minocycline (>8 μg/mL), doxycycline (>8 μg/mL), and amikacin (16-32 μg/mL). The MICs for linezolid, rifabutin, moxifloxacin, ciprofloxacin, streptomycin, clarithromycin, and rifampicin varied among the isolates. High levels of genomic diversity were noted among these strains concerning genome-called single nucleotide polymorphisms and average nucleotide identity. In total, 4,282 genes were shared across all genomes, while 315 unique genes were restricted to one strain. Comparative genomic analysis identified two unique virulence genes encoding a catalase enzyme and a protein involved in capsule biosynthesis and transport. Additionally, all M. seoulense strains demonstrated the ability to survive within macrophages.

The clinical M. seoulense isolates analyzed in this study exhibited varying levels of antibiotic susceptibility, suggesting the potential need for susceptibility testing to guide clinical treatment. Genomic features of these isolates indicated that they are likely pathogenic non-tuberculous mycobacterium, highlighting a need for closer epidemiological monitoring.

## Linked entities

- **Chemicals:** minocycline (PubChem CID 54675783), doxycycline (PubChem CID 54671203), amikacin (PubChem CID 37768), linezolid (PubChem CID 3929), moxifloxacin (PubChem CID 152946), ciprofloxacin (PubChem CID 2764), streptomycin (PubChem CID 5297), clarithromycin (PubChem CID 84029), rifampicin (PubChem CID 135398735), p-Nitrobenzoic acid (PubChem CID 6108)
- **Species:** Mycobacterium seoulense (taxon 386911)

## Full-text entities

- **Genes:** CAT (catalase) [NCBI Gene 847]
- **Diseases:** infections (MESH:D007239)
- **Chemicals:** minocycline (MESH:D008911), 7H10 (-), linezolid (MESH:D000069349), p-Nitrobenzoic acid (MESH:C008629), rifampicin (MESH:D012293), doxycycline (MESH:D004318), streptomycin (MESH:D013307), ciprofloxacin (MESH:D002939), clarithromycin (MESH:D017291), moxifloxacin (MESH:D000077266), rifabutin (MESH:D017828), amikacin (MESH:D000583)
- **Species:** Mycobacterium (genus) [taxon 1763], Mycobacterium seoulense (species) [taxon 386911]

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12009822/full.md

## References

56 references — full list in the complete paper: https://tomesphere.com/paper/PMC12009822/full.md

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Source: https://tomesphere.com/paper/PMC12009822