Evidence map›Paper›PMID 33140283›Full record

ArticleFolia microbiologica2021

Pathogen determination from clinical abscess fluids using metagenomic next-generation sequencing.

Yuxi Zhao, Jinlian Chen, Bing Bai, Yu Wang, Jinxin Zheng, Zhijian Yu, Qiwen Deng, Peiyu Li

Abstract read
PubMed Publisher
In one paragraph

Article in Folia microbiologica, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.2field-weighted citation impact, top 22% of its field
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

9 citing papers in PubMed, 14 citations in OpenAlex.

  1. Trial
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  6. Pyopneumothorax caused byWorld journal of emergency medicine · 2023
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  7. Detection ofOpen life sciences · 2023
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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 at 2 institutions in 1 country.

Yuxi Zhao *Department of Infectious Diseases and Shenzhen Key Laboratory for Endogenous Infection, Shenzhen Nanshan People's Hospital and the 6th Affiliated Hospital of Shenzhen University Health Science Center, Shenzhen, China.
Jinlian Chen *Department of Infectious Diseases and Shenzhen Key Laboratory for Endogenous Infection, Shenzhen Nanshan People's Hospital and the 6th Affiliated Hospital of Shenzhen University Health Science Center, Shenzhen, China.
Bing BaiDepartment of Infectious Diseases and Shenzhen Key Laboratory for Endogenous Infection, Shenzhen Nanshan People's Hospital and the 6th Affiliated Hospital of Shenzhen University Health Science Center, Shenzhen, China.
Yu WangDepartment of Infectious Diseases and Shenzhen Key Laboratory for Endogenous Infection, Shenzhen Nanshan People's Hospital and the 6th Affiliated Hospital of Shenzhen University Health Science Center, Shenzhen, China.
Jinxin ZhengDepartment of Infectious Diseases and Shenzhen Key Laboratory for Endogenous Infection, Shenzhen Nanshan People's Hospital and the 6th Affiliated Hospital of Shenzhen University Health Science Center, Shenzhen, China.
Zhijian YuDepartment of Infectious Diseases and Shenzhen Key Laboratory for Endogenous Infection, Shenzhen Nanshan People's Hospital and the 6th Affiliated Hospital of Shenzhen University Health Science Center, Shenzhen, China.
Qiwen DengDepartment of Infectious Diseases and Shenzhen Key Laboratory for Endogenous Infection, Shenzhen Nanshan People's Hospital and the 6th Affiliated Hospital of Shenzhen University Health Science Center, Shenzhen, China.
Peiyu LiDepartment of Infectious Diseases and Shenzhen Key Laboratory for Endogenous Infection, Affiliated Shenzhen Sixth Hospital of Guangdong Medical University, Shenzhen, China. lpy_email2011@126.com.ORCID http://orcid.org/0000-0002-1001-7485
Shenzhen University Health Science Center · CNGuangdong Medical College · CN

Funding

Natural Science Foundation of Guangdong Province 2020A1515010979provincial medical funds of Guangdong A2018163Science, Technology and Innovation Commission of Shenzhen Municipality of basic research funds JCYJ20180302144340004Science, Technology and Innovation Commission of Shenzhen Municipality of basic research funds JCYJ20180302144345028Science, Technology and Innovation Commission of Shenzhen Municipality of basic research funds JCYJ20180302144431923Science, Technology and Innovation Commission of Shenzhen Municipality of basic research funds JCYJ20180302144721183Science, Technology and Innovation Commission of Shenzhen Municipality of key funds JCYJ20170412143551332Shenzhen Key Medical Discipline Construction Fund SZXK06162Shenzhen Nanshan District Scientific Research Program of the People's Republic of China 2019001Shenzhen Nanshan District Scientific Research Program of the People's Republic of China 2019004Shenzhen Nanshan District Scientific Research Program of the People's Republic of China 2019005Shenzhen Nanshan District Scientific Research Program of the People's Republic of China 2019027
6 · The paper itself

Abstract

Abscesses are often clinically manifested as local necrotic tissues in various organs or systems of the human body, which is commonly caused by microbial infection. Rapid and accurate identification of pathogens from clinical abscetic samples would greatly guide a clinician to make the precise choices of the antimicrobial treatment. Here, this study aimed to investigate the application of metagenomic next-generation sequencing (mNGS) in the microbial detection of clinical samples of abscess fluids from various organs or systems. Nine patients with abscess from various organs or systems were enrolled in this study. The pathogenic bacteria in abscess fluid were detected and compared by the conventional bacterial culture and mNGS respectively. The dominant pathogens of abscess fluids in 8 cases can be found directly from mNGS, dominating over 80% of the total reads abundance of the microbiome. Although the pathogens from 6 cases detected by mNGS were consistent with that from the conventional bacteria culture method, the fastidious obligate anaerobic bacteria in 2 cases additionally detected by mNGS were not found by the conventional culture method. Moreover, complex polymicrobial infection containing Parvimonas micra in one case negatively with conventional bacterial culture were demonstrated by the mNGS method. And the mNGS method can directly reflect the diversity of microbial ecology in the abscess fluids from the different parts of the human body. Conclusively, mNGS can be used as a supplemental method for the pathogen detection of clinically abscess fluids.

Indexed as

AbscessMetagenomicsBacillotaHigh-Throughput Nucleotide SequencingHumansSensitivity and Specificity

Identifiers

PMID33140283
OpenAlexW3096368612

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.