Nanopore Sequencing for smear-negative pulmonary tuberculosis - a multicentre prospective study in China

Author:

Yan Xiaojing1,Yang Guoli2,Wang Yunfei3,Wang Yuqing4,Cheng Jie5,Xu Peisong6,Qiu Xiaoli3,Su Lei7,Liu Lina8,Geng Ruixue9,You Yingxia10,Liu Hui1,Chu Naihui1,Ma Li1,Nie Wenjuan1

Affiliation:

1. Beijing Chest Hospital

2. Tuberculosis Hospital of Jilin Province (Jilin Provincial Infectious Disease Hospital)

3. Hangzhou Shengting Medical Technology

4. The Fourth People's Hospital of Qinghai Province

5. Anhui Provincial Chest Hospital

6. Hangzhou Shengting Medical Technolog, Ltd

7. Henan Province Anyang City Tuberculosis Prevention and Control Institute

8. Hengshui Third People's Hospital

9. Hohhot Second Hospital

10. Zhengzhou Sixth People's Hospital

Abstract

Abstract Purpose: In this prospective study, the diagnosis accuracy of nanopore sequencing-based Mycobacterium tuberculosis (MTB) detection was determined through examining sputum or bronchoalveolar lavage fluid (BALF) samples from pulmonary tuberculosis (PTB) -suspected patients. Compared the diagnostic performance of nanopore sequencing, mycobacterial growth indicator tube (MGIT) culture and Xpert MTB/rifampin resistance (MTB/RIF) assays. Methods: Specimens collected from suspected PTB cases across China from September 2021 to April 2022 were tested then assay diagnostic accuracy rates were compared. Results: Among the 111 suspected PTB cases that were ultimately diagnosed as PTB, the diagnostic rate of nanopore sequencing was statistically significant different from other assays (P < 0.05). Fleiss’ kappa values of 0.219 and 0.303 indicated fair consistency levels between MTB detection results obtained using nanopore sequencing versus other assays, respectively. Respective PTB diagnostic sensitivity rates of MGIT culture, Xpert MTB/RIF and nanopore sequencing of 36.11%, 40.28% and 83.33% indicated superior sensitivity of nanopore sequencing. Analysis of area under the curve (AUC), Youden’s index and accuracy values and the negative predictive value (NPV) indicated superior MTB detection performance for nanopore sequencing (with Xpert MTB/RIF ranking second), while the PTB diagnostic accuracy rate of nanopore sequencing exceeded corresponding rates of the other methods. Conclusions: In comparison with MGIT culture and Xpert MTB/RIF assays, BALF’s nanopore sequencing provided superior MTB detection sensitivity and thus is suitable for testing of sputum-scarce suspected PTB cases. However, negative results obtained using these assays should be confirmed based on additional evidence before ruling out a PTB diagnosis.

Publisher

Research Square Platform LLC

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