Diagnosis of Non-Tuberculous Mycobacterial Pulmonary Disease by Metagenomic Next-Generation Sequencing on Bronchoalveolar Lavage Fluid

被引:8
|
作者
Zhang, Xuan [1 ]
Chen, Huixin [1 ]
Lin, Yaqing [2 ]
Yang, Meifang [1 ]
Zhao, Hong [1 ]
Hu, Jianhua [1 ]
Han, Dongsheng [3 ,4 ,5 ,6 ]
机构
[1] Zhejiang Univ, Affiliated Hosp 1, Natl Clin Res Ctr Infect Dis, Sch Med,Collaborat Innovat Ctr Diag & Treatment In, Hangzhou, Zhejiang, Peoples R China
[2] Zhejiang Shuren Univ, Shulan Hangzhou Hosp, Shulan Int Med Coll, Hangzhou, Zhejiang, Peoples R China
[3] Zhejiang Univ, Affiliated Hosp 1, Dept Lab Med, Sch Med, Hangzhou, Zhejiang, Peoples R China
[4] Key Lab Clin In Vitro Diagnost Tech Zhejiang Prov, Hangzhou, Zhejiang, Peoples R China
[5] Zhejiang Univ, Inst Lab Med, Hangzhou, Zhejiang, Peoples R China
[6] Zhejiang Univ, Affiliated Hosp 1, Coll Med, Ctr Clin Lab, 79 Qingchun Rd, Hangzhou 310003, Peoples R China
来源
关键词
non-tuberculous mycobacterial; culture; metagenomic next-generation sequencing; bronchoalveolar lavage fluid; HEALTH;
D O I
10.2147/IDR.S417088
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Purpose: Metagenomic next-generation sequencing (mNGS) has been extensively used in the diagnosis of infectious diseases but has rarely been applied in non-tuberculous mycobacterial pulmonary disease (NTMPD). This study analyzed the diagnostic performance of mNGS in bronchoalveolar lavage fluid (BALF) samples to identify non-tuberculous mycobacteria (NTM). Patients and Methods: A total of 231 patients with suspected NTMPD were recruited from the First Affiliated Hospital, School of Medicine, Zhejiang University, from March 2021 to October 2022. A total of 118 cases were ultimately included. Of these patients, 61 cases were enrolled in the NTMPD group, 23 cases were enrolled in the suspected-NTMPD group, and 34 cases were enrolled in the non-NTMPD group. The diagnostic performance of traditional culture, acid-fast staining (AFS), and mNGS for NTMPD was assessed. Results: Patients in the NTMPD group had a higher proportion of bronchiectasis (P=0.007). Among mNGS-positive samples in the NTMPD group, a significantly higher reads number of NTM was observed in AFS-positive patients [61.50 (22.00, 395.00) vs 15.50 (6.00, 36.25), P=0.008]. Meanwhile, mNGS demonstrated a sensitivity of 90.2%, which was far superior to AFS (42.0%) and culture (77.0%) (P<0.001). The specificity of mNGS in detecting NTM was 100%, which was the same as that of traditional culture. The area under the receiver operating characteristic curve of mNGS was 0.951 (95% CI 0.906-0.996), which was higher than that of culture (0.885 [95% CI 0.818-0.953]) and AFS (0.686 [95% CI 0.562-0.810]). In addition to NTM, other pulmonary pathogens were also found by mNGS. Conclusion: mNGS using BALF samples is a rapid and effective diagnostic tool for NTMPD, and mNGS is recommended for patients with suspected NMTPD or NTM coinfected pneumonia.
引用
收藏
页码:4137 / 4145
页数:9
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