Evidence map›Paper›PMID 39419957›Full record

ArticleInfection2025

Targeted next-generation sequencing - a promising approach in the diagnosis of Mycobacterium tuberculosis and drug resistance.

Xiaocui Wu, Guangkun Tan, Chunlei Sun, Yang Wang, Jinghui Yang, Chunqiu Wu, Chaohui Hu, Fangyou Yu

Abstract read
In one paragraph

Article in Infection, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

20 citing papers in PubMed.

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  9. Infantile pulmonary abscess due toFrontiers in pediatrics · 2026
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Xiaocui Wu *Department of Clinical Laboratory, Shanghai Pulmonary Hospital, School of Medicine, Tongji University, Shanghai, China.
Guangkun Tan *Department of Clinical Laboratory, Shanghai University of Traditional Chinese Medical Attached Shuguang Hospital, Shanghai, China.
Chunlei Sun *Department of Clinical Laboratory, Shanghai Eye Disease Prevention & Treatment Center, Shanghai Eye Hospital, Shanghai, China.
Yang WangGuangzhou KingCreate Biotechnology Co., Ltd., Guangzhou, China.
Jinghui YangDepartment of Clinical Laboratory, Shanghai Pulmonary Hospital, School of Medicine, Tongji University, Shanghai, China.
Chunqiu WuGuangzhou KingCreate Biotechnology Co., Ltd., Guangzhou, China.
Chaohui HuGuangzhou KingCreate Biotechnology Co., Ltd., Guangzhou, China. huzh@kingcreate.com.cn.
Fangyou YuDepartment of Clinical Laboratory, Shanghai Pulmonary Hospital, School of Medicine, Tongji University, Shanghai, China. wzjxyfy@163.com.

Funding

Shanghai Municipal Health Commission's Special Youth Project for Clinical Research in the Health Industry 20224Y0129Shanghai Science and Technology Innovation Action Plan, Medical Innovation Research Special Project 22Y11902600Shanghai Three-year (2023-2025) Action Plan to Strengthen the Public Health System GWVI-11.1-05Shanghai Three-year (2023-2025) Action Plan to Strengthen the Public Health System . GWVI-11.2-YQ52
6 · The paper itself

Abstract

Targeted next-generation sequencing (tNGS) offers a high-throughput, culture-independent approach that delivers a comprehensive resistance profile in a significantly shorter turn-around time, making it promising in enhancing tuberculosis (TB) diagnosis and informing treatment decisions. This study aims to evaluate the performance of tNGS in the TB diagnosis and drug resistance detection of Mycobacterium tuberculosis (MTB) using MTB clinical isolates and bronchoalveolar lavage fluid (BALF) samples. A total of 143 MTB clinical isolates were assessed, tNGS, phenotypic antimicrobial susceptibility testing (AST), and AST based on whole genome sequencing (WGS) exhibited high concordance rates, averaging 95.10% and 97.05%. Among 158 BALF samples, culture, Xpert MTB/RIF, and tNGS reported 29, 70 and 111 positives, respectively. In the confirmed cases with etiological evidence (smears, cultures, or molecular test), the positive rate of tNGS (73/83, 87.95%) was higher than that of Xpert MTB (67/83, 80.72%). Additionally, 45% (27/60) of clinically diagnosed cases (with imaging or immunological evidence) were positive for tNGS. Further validation on the discrepant results between tNGS and Xpert MTB/RIF with droplet digital PCR (ddPCR) yielded 35 positives, tNGS detected all, and Xpert MTB/RIF only identified 6 positives. In conclusion, tNGS demonstrates robust and rapid performance in the identification of MTB and its associated drug resistance, and can be directly applied to clinical samples, positioning it as a promising approach for laboratory testing of tuberculosis.

Indexed as

Drug Resistance, BacterialHigh-Throughput Nucleotide SequencingMycobacterium tuberculosisTuberculosisTuberculosis, Multidrug-ResistantAdultAntitubercular AgentsBronchoalveolar Lavage FluidFemaleHumansMaleMicrobial Sensitivity TestsWhole Genome SequencingAntitubercular AgentsDiagnosisDrug resistanceMycobacterium tuberculosisTargeted next-generation sequencing

Identifiers

PMID39419957
PMCPMC12137396

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.