Evidence map›Paper›PMID 41699716›Full record

ArticleGut pathogens2026

Enhanced pathogen detection and gut microbiome alterations in pyogenic liver abscess: insights from next-generation sequencing.

Ju Sun Song, Young Kul Jung, Solbi Kweon, Seong-Hee Kang, Hyung Joon Yim, Seung Kak Shin, Gwang Hyeon Choi, Eun Sun Jang, Hae Lim Lee, Sung Won Lee and 7 more

Abstract read
In one paragraph

Article in Gut pathogens, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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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

17 authors.

Ju Sun Song *Department of Laboratory Medicine, GC Genome, Green Cross Laboratories, Seoul, Republic of Korea.
Young Kul Jung *Division of Gastroenterology and Hepatology, Department of Internal Medicine, Korea University Ansan Hospital, Ansan, Republic of Korea.
Solbi KweonDepartment of Laboratory Medicine, GC Genome, Green Cross Laboratories, Seoul, Republic of Korea.
Seong-Hee KangDivision of Gastroenterology and Hepatology, Department of Internal Medicine, Korea University Ansan Hospital, Ansan, Republic of Korea.
Hyung Joon YimDivision of Gastroenterology and Hepatology, Department of Internal Medicine, Korea University Ansan Hospital, Ansan, Republic of Korea.
Seung Kak ShinDepartment of Internal Medicine, Gil Medical Center, Gachon University College of Medicine, Incheon, Republic of Korea.
Gwang Hyeon ChoiDepartment of Internal Medicine, Seoul National University Bundang Hospital, Seoul National University College of Medicine, Seongnam-si, Republic of Korea.
Eun Sun JangDepartment of Internal Medicine, Seoul National University Bundang Hospital, Seoul National University College of Medicine, Seongnam-si, Republic of Korea.
Hae Lim LeeDepartment of Internal Medicine, Bucheon St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Incheon, Republic of Korea.
Sung Won LeeDepartment of Internal Medicine, Bucheon St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Incheon, Republic of Korea.
Jung Hwan YuDepartment of Internal Medicine, Inha University Hospital, Inha University School of Medicine, Incheon, Republic of Korea.
Ji Eun HanDepartment of Gastroenterology, Ajou University School of Medicine, Suwon, Republic of Korea.
Soon Sun KimDepartment of Gastroenterology, Ajou University School of Medicine, Suwon, Republic of Korea.
Sang Gyune KimDivision of Gastroenterology and Hepatology, Department of internal medicine, Soonchunhyang University Bucheon Hospital, 170 Jomaruro Wonmigu, Bucheonsi, 14584, Gyeonggido, Republic of Korea.
Young Seok KimDivision of Gastroenterology and Hepatology, Department of internal medicine, Soonchunhyang University Bucheon Hospital, 170 Jomaruro Wonmigu, Bucheonsi, 14584, Gyeonggido, Republic of Korea.
Min Jae Kim *Department of Infectious Diseases Asan Medical Center, University of Ulsan College of Medicine, 88 Olympic-ro 43 Gil, Songpa-gu, Seoul, 05505, Republic of Korea. nahani99@gmail.com.
Jeong-Ju Yoo *Division of Gastroenterology and Hepatology, Department of internal medicine, Soonchunhyang University Bucheon Hospital, 170 Jomaruro Wonmigu, Bucheonsi, 14584, Gyeonggido, Republic of Korea. puby17@naver.com.

Funding

Asan Medical Center fund 2020IF0005
6 · The paper itself

Abstract

objectivesPyogenic liver abscess (PLA) is a life-threatening infection with high mortality in Asia. Although Klebsiella pneumoniae is commonly implicated, emerging data suggest a more diverse microbial spectrum. This study investigated pathogen detection using conventional culture and next-generation sequencing (NGS) and characterized gut microbiome alterations in PLA patients compared to healthy controls.

methodThis was a prospective, multicenter cohort study conducted across eight tertiary hospitals. We enrolled 100 PLA patients who underwent percutaneous aspiration. Abscess aspirates underwent both conventional culture and 16 S rRNA-based NGS. Stool samples from PLA patients and 100 healthy controls were analyzed for gut microbiome composition using NGS.

resultsCulture positivity was 82%, with abscess cultures positive in 77 cases and blood cultures in 32. K. pneumoniae was the most frequently isolated pathogen (67%), and polymicrobial infections were identified in only 3% of cases by culture. NGS of abscess aspirates was available in 92% of patients, including 15 culture-negative cases. NGS identified polymicrobial infections in 16.3% of patients-more than fivefold higher than culture. Among 77 patients who underwent both culture and NGS, 13 (16.9%) showed discordance, mostly due to polymicrobial or anaerobic organisms identified by NGS. Stool NGS analysis revealed significantly reduced alpha diversity in PLA patients compared to healthy controls (Shannon index 2.9 vs. 3.5, p < 0.001), increased abundance of Enterococcus species (27.1% vs. 8.6%, p < 0.001), and depletion of SCFA-producing genera including Faecalibacterium, Roseburia, and Lachnospira species. Despite K. pneumoniae dominance in abscesses, its stool abundance did not significantly differ between PLA patients and controls.

conclusionNGS improves the detection of anaerobes and mixed infections in PLA. The gut microbiota of PLA patients shows marked dysbiosis, suggesting a potential role in disease pathogenesis and future therapeutic targets.

Indexed as

Gut-liver axisGut microbiomeNext generation sequencingPyogenic liver abscess

Identifiers

PMID41699716
PMCPMC12922343

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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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 Socratic graph.