Evidence map›Paper›PMID 41120658›Full record

ArticleProbiotics and antimicrobial proteins2026

Restoration of the Mucosal Barrier by Lactobacillus gasseri HDS0266 and Enterococcus faecium HDS0288 in Dextran Sodium Sulfate and Clostridioides difficile-Induced Colitis Mice.

Eunjung Kim, Bobae Kim, Haeun Kim, Dongyeol Kim, Ju Yeong Kim, Jun Ho Choi, Sun-Ju Oh, Minjae Lee, Woorim Park, Hoyeon Kim and 2 more

Abstract read
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In one paragraph

Article in Probiotics and antimicrobial proteins, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Frontiers in microbiology · 2026
    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

12 authors.

Eunjung KimSchool of Life Science, Handong Global University, Pohang, 37554, Republic of Korea.
Bobae KimSchool of Life Science, Handong Global University, Pohang, 37554, Republic of Korea.
Haeun KimSchool of Life Science, Handong Global University, Pohang, 37554, Republic of Korea.
Dongyeol KimSchool of Life Science, Handong Global University, Pohang, 37554, Republic of Korea.
Ju Yeong KimDepartment of Tropical Medicine, Institute of Tropical Medicine, Arthropods of Medical Importance Resource Bank, Yonsei University College of Medicine, Seoul, 03722, Republic of Korea.
Jun Ho ChoiDepartment of Tropical Medicine, Institute of Tropical Medicine, Arthropods of Medical Importance Resource Bank, Yonsei University College of Medicine, Seoul, 03722, Republic of Korea.
Sun-Ju OhDepartment of Pathology, Kosin University College of Medicine, Busan, 49267, Republic of Korea.
Minjae LeeSchool of Life Science, Handong Global University, Pohang, 37554, Republic of Korea.
Woorim ParkSchool of Life Science, Handong Global University, Pohang, 37554, Republic of Korea.
Hoyeon KimSchool of Life Science, Handong Global University, Pohang, 37554, Republic of Korea.
Wilhelm H HolzapfelDepartment of Advanced Convergence, Handong Global University, Pohang, 37554, Republic of Korea. wilhelm@woodapple.net.
Hongsup YoonSchool of Life Science, Handong Global University, Pohang, 37554, Republic of Korea. hong@handong.edu.

Funding

Handong Global University Research Grants No. 202300560001
6 · The paper itself

Abstract

Inflammatory bowel disease (IBD), which includes Crohn's disease and ulcerative colitis, along with Clostridioides difficile (C. difficile) infection (CDI), are significant gastrointestinal disorders characterized by microbial dysbiosis and influenced by environmental factors. The success of current treatments for IBD and CDI, such as anti-inflammatory drugs and antibiotics, is limited by recurrence, antibiotic resistance, and disruption of healthy gut microbiota. These limitations have given rise to increased interest in probiotics as alternative, adjuvant therapies for both IBD and CDI. In this study, we evaluated the therapeutic potential of two probiotic strains, Enterococcus faecium HDS0288 and Lactobacillus gasseri HDS0266, in a dextran sodium sulfate (DSS) and CDI-induced colitis mouse model, which replicates key aspects of both IBD and CDI. Administration of the combination of E. faecium HDS0288 and L. gasseri HDS0266 led to significant improvements in intestinal barrier function, including increased goblet cell numbers and enhanced integrity of the mucus barrier, all of which contributed to the intestinal epithelium recovery. Our findings demonstrate that E. faecium HDS0288 and L. gasseri HDS0266 may serve as promising adjuvant therapies for the treatment of both IBD and CDI by promoting restoration of epithelial integrity and intestinal barrier function.

Indexed as

Clostridium InfectionsColitisEnterococcus faeciumIntestinal MucosaLactobacillus gasseriProbioticsAnimalsClostridioides difficileDextran SulfateDisease Models, AnimalFemaleMaleMiceMice, Inbred C57BLDextran SulfateAdjuvant therapiesClostridioides difficile infectionInflammatory bowel diseaseMucosal barrierProbiotics

Identifiers

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.