Evidence map›Paper›PMID 40221512›Full record

ArticleScientific reports2025

The clinical value of metagenomic next-generation sequencing in the diagnosis of pulmonary tuberculosis and the exploration of lung microbiota characteristics.

Yan Yong, Lihong Zhou, Xiaojing Zhang, Xiaoqin Ran, Yuxin Guo, Wei Gai, Yuanyuan Chen

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

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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

3 citing papers in PubMed.

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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

7 authors.

Yan Yong *Zhejiang Tuberculosis Diagnosis and Treatment Center, Zhejiang Hospital of Integrated Traditional Chinese and Western Medicine, No. 208 Huancheng East Road, Hangzhou, China.
Lihong Zhou *Zhejiang Tuberculosis Diagnosis and Treatment Center, Zhejiang Hospital of Integrated Traditional Chinese and Western Medicine, No. 208 Huancheng East Road, Hangzhou, China.
Xiaojing Zhang *WillingMed Technology (Beijing) Co., Ltd, No. 156 Jinghai 4th Road, Beijing Economic and Technological Development Zone, Beijing, China.
Xiaoqin RanZhejiang Tuberculosis Diagnosis and Treatment Center, Zhejiang Hospital of Integrated Traditional Chinese and Western Medicine, No. 208 Huancheng East Road, Hangzhou, China.
Yuxin GuoWillingMed Technology (Beijing) Co., Ltd, No. 156 Jinghai 4th Road, Beijing Economic and Technological Development Zone, Beijing, China.
Wei GaiWillingMed Technology (Beijing) Co., Ltd, No. 156 Jinghai 4th Road, Beijing Economic and Technological Development Zone, Beijing, China. weigai@willingmed.com.
Yuanyuan ChenZhejiang Tuberculosis Diagnosis and Treatment Center, Zhejiang Hospital of Integrated Traditional Chinese and Western Medicine, No. 208 Huancheng East Road, Hangzhou, China. dryuanyuan_chen@sina.com.

Funding

National Natural Science Foundation of China 82104236
6 · The paper itself

Abstract

The lung microbiota plays a critical role in many important physiological processes and is linked with various pulmonary infectious diseases. The present study aimed to characterize the lung microbiota in patients with pulmonary tuberculosis (PTB), and to explore the association between the abundance of Mycobacterium tuberculosis complex (MTBC) and the lung microbiota. This retrospective study included 190 patients with MTBC infection. The enrolled patients were classified into three groups based on the abundance results of bronchoalveolar lavage fluid (BALF) mNGS: low [reads per ten million (RPTM) = 1 ~ 1000], medium (RPTM = 1001 ~  10000) and high (RPTM > 10000). In the high-abundance group, there were more bilateral lobar involvement and symptoms of cavitation. In addition to mNGS, the highest positivity rates were T-spot (92.36%), GeneXpert (71.58%), culture (68.95%) and AFB smear (17.84%). The positive rates of culture, AFB smear and GeneXpert increased with the increase of MTBC abundance, and the positive rates were highest in the high-abundance MTBC group. Both the alpha and beta diversity showed significant difference between the three groups, with the high-abundance MTBC groups showed lowest alpha diversity. The increased abundance of MTBC positively associated with the longer time of hospital stay. To sum up, the lung microbiota of patients with PTB were significantly distinct between groups with different abundant levels of MTBC. Combined with imaging features, a high abundance of MTBC suggests the patient is more severely ill and has a poorer prognosis.

Indexed as

High-Throughput Nucleotide SequencingLungMetagenomicsMicrobiotaMycobacterium tuberculosisTuberculosis, PulmonaryAdultAgedBronchoalveolar Lavage FluidFemaleHumansMaleMiddle AgedRetrospective StudiesAbundanceLung microbiotaMycobacterium tuberculosis complexPulmonary tuberculosis

Identifiers

PMID40221512
PMCPMC11993618

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