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Background <p><i>Mycolicibacterium houstonense</i> is prone to being misidentified as other mycobacteria, particularly <i>M. fortuitum</i>. This study characterized the genome of a clinical <i>M. houstonense</i> isolate and delineated its phylogenetic relationship with <i>M. fortuitum</i> to provide a basis for accurate diagnosis and management of infections caused by this species.</p> Methods <p>Genome sequencing was used to determine the taxonomic status, virulence profile, and resistance traits of the clinical isolate, while comparative genomics was employed to delineate its evolutionary relationship with <i>M. fortuitum</i>.</p> Results <p>The clinical isolate was definitively identified as <i>M. houstonense</i>. Genomic analysis revealed a unique repertoire of virulence and resistance genes. Its genome harbors 590 virulence genes, many of which encode T7SS effectors. In addition to resistance genes commonly found in nontuberculous mycobacteria, it also carries <i>M. tuberculosis</i>-related resistance determinants, enhancing its resilience to disinfectants, antiseptics, and antimicrobials commonly used in clinical settings. Phylogenomic analysis indicates that <i>M. houstonense</i> and <i>M. fortuitum</i> drive reciprocal divergence, reinforcing their environmental adaptability.</p> Conclusion <p>Genomic analysis is poised to serve as a robust tool for the identification of <i>M. houstonense</i>. The clinical isolate in our study suggests a potential dual escalation of <i>M. houstonense</i> in adaptability and virulence, underscoring the need for stricter clinical monitoring and environmental surveillance.</p>

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Genomic analysis of a clinical Mycolicibacterium houstonense isolate reveals dual escalation in adaptability and virulence

  • 期刊论文

  • 出版模式：

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  • 发表日期：

    2025年12月20日

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  • Ailing Xu,
  • Nifang Pan,
  • Bibo Zhang,
  • Xuan Liu,
  • Yuefeng Sheng,
  • Yimai Deng,
  • Zhenghao Wu,
  • Shuyan Wu

摘要

Background

Mycolicibacterium houstonense is prone to being misidentified as other mycobacteria, particularly M. fortuitum. This study characterized the genome of a clinical M. houstonense isolate and delineated its phylogenetic relationship with M. fortuitum to provide a basis for accurate diagnosis and management of infections caused by this species.

Methods

Genome sequencing was used to determine the taxonomic status, virulence profile, and resistance traits of the clinical isolate, while comparative genomics was employed to delineate its evolutionary relationship with M. fortuitum.

Results

The clinical isolate was definitively identified as M. houstonense. Genomic analysis revealed a unique repertoire of virulence and resistance genes. Its genome harbors 590 virulence genes, many of which encode T7SS effectors. In addition to resistance genes commonly found in nontuberculous mycobacteria, it also carries M. tuberculosis-related resistance determinants, enhancing its resilience to disinfectants, antiseptics, and antimicrobials commonly used in clinical settings. Phylogenomic analysis indicates that M. houstonense and M. fortuitum drive reciprocal divergence, reinforcing their environmental adaptability.

Conclusion

Genomic analysis is poised to serve as a robust tool for the identification of M. houstonense. The clinical isolate in our study suggests a potential dual escalation of M. houstonense in adaptability and virulence, underscoring the need for stricter clinical monitoring and environmental surveillance.