Evidence map›Paper›PMID 36517824›Full record

ArticleRespiratory research2022

Evaluation of respiratory samples in etiology diagnosis and microbiome characterization by metagenomic sequencing.

Qing Miao, Tianzhu Liang, Na Pei, Chunjiao Liu, Jue Pan, Na Li, Qingqing Wang, Yanqiong Chen, Yu Chen, Yuyan Ma and 11 more

Abstract read
In one paragraph

Article in Respiratory research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing 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

18 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Lower respiratory tract microbiota characteristics in patients withFrontiers in cellular and infection microbiology · 2026
    Article
  5. Article
  6. ChronicInfection and drug resistance · 2026
    Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. The respiratory tract virome: unravelling the role of viral dark matter in respiratory health and disease.European respiratory review : an official journal of the European Respiratory Society · 2025
    Review
  12. Article
  13. Comparison of molecular testing methods for diagnosing non-tuberculous mycobacterial infections.European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology · 2025
    Article
  14. Article
  15. Observational
  16. Article
  17. Article
  18. Article
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

21 authors.

Qing Miao *Department of Infectious Diseases, Zhongshan Hospital of Fudan University, Shanghai, 200032, China.
Tianzhu Liang *BGI-Shenzhen, Shenzhen, 518083, China.
Na Pei *BGI-Shenzhen, Shenzhen, 518083, China. peina@genomics.cn.
Chunjiao Liu *BGI-Shenzhen, Shenzhen, 518083, China.
Jue PanDepartment of Infectious Diseases, Zhongshan Hospital of Fudan University, Shanghai, 200032, China.
Na LiDepartment of Infectious Diseases, Zhongshan Hospital of Fudan University, Shanghai, 200032, China.
Qingqing WangDepartment of Infectious Diseases, Zhongshan Hospital of Fudan University, Shanghai, 200032, China.
Yanqiong ChenDepartment of Infectious Diseases, Zhongshan Hospital of Fudan University, Shanghai, 200032, China.
Yu ChenDepartment of Infectious Diseases, Zhongshan Hospital of Fudan University, Shanghai, 200032, China.
Yuyan MaDepartment of Infectious Diseases, Zhongshan Hospital of Fudan University, Shanghai, 200032, China.
Wenting JinDepartment of Infectious Diseases, Zhongshan Hospital of Fudan University, Shanghai, 200032, China.
Yao ZhangDepartment of Infectious Diseases, Zhongshan Hospital of Fudan University, Shanghai, 200032, China.
Yi SuDepartment of Infectious Diseases, Zhongshan Hospital of Fudan University, Shanghai, 200032, China.
Yumeng YaoDepartment of Infectious Diseases, Zhongshan Hospital of Fudan University, Shanghai, 200032, China.
Yingnan HuangDepartment of Infectious Diseases, Zhongshan Hospital of Fudan University, Shanghai, 200032, China.
Chunmei ZhouDepartment of Microbiology, Zhongshan Hospital of Fudan University, Shanghai, 200032, China.
Rong BaoDepartment of Microbiology, Zhongshan Hospital of Fudan University, Shanghai, 200032, China.
Xiaoling XuBGI-Shenzhen, Shenzhen, 518083, China.
Weijun ChenBGI-Shenzhen, Shenzhen, 518083, China.
Bijie HuDepartment of Infectious Diseases, Zhongshan Hospital of Fudan University, Shanghai, 200032, China. hu.bijie@zs-hospital.sh.cn.
Junhua LiBGI-Shenzhen, Shenzhen, 518083, China. lijunhua@genomics.cn.

Funding

Clinical Research Plan of Shanghai Hospital Development Center SHDC2020CR2031B
6 · The paper itself

Abstract

backgroundThe application of clinical mNGS for diagnosing respiratory infections improves etiology diagnosis, however at the same time, it brings new challenges as an unbiased sequencing method informing all identified microbiomes in the specimen.

methodsStrategy evaluation and metagenomic analysis were performed for the mNGS data generated between March 2017 and October 2019. Diagnostic strengths of four specimen types were assessed to pinpoint the more appropriate type for mNGS diagnosis of respiratory infections. Microbiome complexity was revealed between patient cohorts and infection types. A bioinformatic pipeline resembling diagnosis results was built based upon multiple bioinformatic parameters.

resultsThe positive predictive values (PPVs) for mNGS diagnosing of non-mycobacterium, Nontuberculous Mycobacteria (NTM), and Aspergillus were obviously higher in bronchoalveolar lavage fluid (BALF) demonstrating the potency of BALF in mNGS diagnosis. Lung tissues and sputum were acceptable for diagnosis of the Mycobacterium tuberculosis (MTB) infections. Interestingly, significant taxonomy differences were identified in sufficient BALF specimens, and unique bacteriome and virome compositions were found in the BALF specimens of tumor patients. Our pipeline showed comparative diagnostic strength with the clinical microbiological diagnosis.

conclusionsTo achieve reliable mNGS diagnosis result, BALF specimens for suspicious common infections, and lung tissues and sputum for doubtful MTB infections are recommended to avoid the false results given by the complexed respiratory microbiomes. Our developed bioinformatic pipeline successful helps mNGS data interpretation and reduces manual corrections for etiology diagnosis.

Indexed as

MicrobiotaMycobacterium tuberculosisRespiratory Tract InfectionsBronchoalveolar Lavage FluidHumansMetagenomicsSensitivity and SpecificityBronchoalveolar lavage fluidClinical metagenomicMicrobiome characterization

Identifiers

PMID36517824
PMCPMC9748891

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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.