The Value of Single-Molecule Nanopore DNA Sequencing in the Clinical Diagnosis of Suspected Tuberculosis Patients.

IF 0.7 4区 医学 Q4 MEDICAL LABORATORY TECHNOLOGY
Jie Cheng, Song Zheng, Ling Peng, Mei Li, Dianchao Wang, Yong Li, Rong Ma
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引用次数: 0

Abstract

Background: Early diagnosis of Mycobacterium tuberculosis (MTB) infection is of great significance for the clinical management of tuberculosis (TB). We first explored the efficacy of single-molecule nanopore DNA sequencing in the early diagnosis of suspected TB patients and analyzed the advantages in differentiating and diagnosing MTB and non-tuberculous Mycobacteria (NTM).

Methods: In this cohort study, we reviewed the clinical data of suspected TB patients admitted from December 1, 2021, through April 15, 2022. All patients underwent 3 - 6 times acid-fast bacilli smear examinations of sputum, all of which were negative. To make a definitive diagnosis, we extracted specimens from the patients and performed specimen culture, Xpert MTB/Rif assay, and single-molecule nanopore DNA sequencing. The efficacy of different diagnostic methods in diagnosing suspected TB patients was compared using "Diagnostic Criteria for Pulmonary Tuberculosis" (WS288-2017) as the gold standard.

Results: Among the 25 patients, 15 were infected with MTB, 5 were infected with NTM, 1 had mixed MTB and NTM infection, and 4 were negative. The accuracy of single-molecule nanopore DNA sequencing in diagnosing mycobacterial infection (MTB + NTM) was 92.0%, with a sensitivity of 90.5% and a specificity of 100%; the accuracy of diagnosing MTB infection was also 92.0%, with a sensitivity of 87.5% and a specificity of 100%. Single-molecule nanopore DNA sequencing showed an accuracy of 100% in differentiating MTB and NTM. However, the diagnostic accuracy and sensitivity of specimen culture and Xpert MTB/Rif assay were relatively low (≤ 52%) compared to "specimen culture + Xpert MTB/Rif assay". The diagnostic efficacy of single-molecule nanopore DNA sequencing was not affected by the source of tissue samples, while specimen culture and Xpert MTB/Rif assay could not diagnose mycobacterial infection using extrapulmonary specimens.

Conclusions: As a third-generation sequencing technology, single-molecule nanopore DNA sequencing has significant application value in diagnosing suspected TB patients. Compared to traditional diagnostic methods, such as specimen culture and Xpert MTB/Rif assay, single-molecule nanopore DNA sequencing exhibits high diagnostic efficacy, low error rate, and convenient detection.

单分子纳米孔DNA测序在疑似肺结核患者临床诊断中的价值。
背景:结核分枝杆菌(MTB)感染的早期诊断对结核病的临床治疗具有重要意义。首先探讨单分子纳米孔DNA测序在疑似结核患者早期诊断中的作用,分析其在MTB和非结核分枝杆菌(NTM)鉴别诊断中的优势。方法:在这项队列研究中,我们回顾了从2021年12月1日到2022年4月15日住院的疑似结核病患者的临床资料。所有患者均行3 ~ 6次痰抗酸杆菌涂片检查,均为阴性。为了做出明确的诊断,我们从患者身上提取标本,进行标本培养、Xpert MTB/Rif测定和单分子纳米孔DNA测序。以《肺结核诊断标准》(WS288-2017)为金标准,比较不同诊断方法对疑似结核病患者的诊断效果。结果:25例患者中MTB感染15例,NTM感染5例,MTB与NTM混合感染1例,阴性4例。单分子纳米孔DNA测序诊断分枝杆菌感染(MTB + NTM)的准确率为92.0%,灵敏度为90.5%,特异性为100%;诊断结核分枝杆菌感染的准确率为92.0%,敏感性为87.5%,特异性为100%。单分子纳米孔DNA测序对MTB和NTM的鉴别准确率为100%。然而,与“标本培养+ Xpert MTB/Rif检测”相比,标本培养+ Xpert MTB/Rif检测的诊断准确性和灵敏度相对较低(≤52%)。单分子纳米孔DNA测序的诊断效果不受组织样本来源的影响,而标本培养和Xpert MTB/Rif检测不能诊断肺外标本的分枝杆菌感染。结论:单分子纳米孔DNA测序作为第三代测序技术,在诊断疑似结核病患者中具有重要的应用价值。与传统的标本培养、Xpert MTB/Rif检测等诊断方法相比,单分子纳米孔DNA测序具有诊断效率高、错误率低、检测方便等优点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Clinical laboratory
Clinical laboratory 医学-医学实验技术
CiteScore
1.50
自引率
0.00%
发文量
494
审稿时长
3 months
期刊介绍: Clinical Laboratory is an international fully peer-reviewed journal covering all aspects of laboratory medicine and transfusion medicine. In addition to transfusion medicine topics Clinical Laboratory represents submissions concerning tissue transplantation and hematopoietic, cellular and gene therapies. The journal publishes original articles, review articles, posters, short reports, case studies and letters to the editor dealing with 1) the scientific background, implementation and diagnostic significance of laboratory methods employed in hospitals, blood banks and physicians'' offices and with 2) scientific, administrative and clinical aspects of transfusion medicine and 3) in addition to transfusion medicine topics Clinical Laboratory represents submissions concerning tissue transplantation and hematopoietic, cellular and gene therapies.
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