Diagnostic value of third-generation nanopore sequencing in extrapulmonary tuberculosis

Front Cell Infect Microbiol. 2025 Jan 7:14:1432446. doi: 10.3389/fcimb.2024.1432446. eCollection 2024.

Abstract

Background: This study aimed to explore the accuracy of third-generation nanopore sequencing to diagnose extrapulmonary tuberculosis (EPTB).

Methods: Samples were collected from the lesions of 67 patients with suspected EPTB admitted between April 2022 and August 2023. Nanopore sequencing, acid-fast bacilli (AFB) staining, DNA testing, and X-pert and mycobacterial cultures were performed. The sensitivity, specificity, positive predictive value (PPV), negative predictive value (NPV) and area under the receiver operating characteristic curve (AUC) were calculated for different diagnostic methods, and their diagnostic accuracies were compared.

Results: Nanopore sequencing demonstrated the highest correct diagnosis rate among 50 positive EPTB cases, independently diagnosing 19 positive cases missed by conventional methods. Its sensitivity (62.00%), specificity (94.10%), PPV (96.90%), NPV (45.70%) and AUC (0.781, 95% CI: 0.67-0.89) were superior to those of conventional methods, such as AFB staining, DNA testing, X-pert, and solid culture, indicating its significantly efficient advantage in EPTB detection.

Conclusion: Nanopore sequencing technology significantly outperforms conventional methods such as AFB staining, DNA testing, X-pert, and mycobacterial culture to diagnose EPTB, promising to improve the diagnosis of EPTB.

Keywords: clinical microbiology; conventional methods; diagnostic value; extrapulmonary tuberculosis; nanopore sequencing.

MeSH terms

  • Adult
  • Aged
  • DNA, Bacterial / genetics
  • Female
  • Humans
  • Male
  • Middle Aged
  • Mycobacterium tuberculosis* / genetics
  • Mycobacterium tuberculosis* / isolation & purification
  • Nanopore Sequencing* / methods
  • Predictive Value of Tests
  • ROC Curve
  • Sensitivity and Specificity*
  • Tuberculosis* / diagnosis
  • Tuberculosis* / microbiology
  • Tuberculosis, Extrapulmonary
  • Young Adult

Substances

  • DNA, Bacterial

Grants and funding

The author(s) declare financial support was received for the research, authorship, and/or publication of this article. This work was supported by the Guangxi Zhuang Autonomous Region Health Commission Selffinanced Scientific Research Project (Z-A20231211); The Health Commission of Guangxi Zhuang Autonomous Region Natural Science Project (Z20211324).