Evidence map›Paper›PMID 41168250›Full record

ArticleScientific reports2025

Insight into immunoregulatory and neuromodulatory capability of Bacteroides cellulosilyticus and Bacteroides xylanisolvens human gut microbiota isolates.

Miroslav Dinić, Jelena Đokić, Stefan Jakovljević, Emilija Brdarić, Hristina Mitrović, Aleksandar Bisenić, Dušan Radojević, Svetlana Soković Bajić, Sergej Tomić, Nataša Golić

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 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Review
  2. Article
  3. Detoxification of Ochratoxin A byFoods (Basel, Switzerland) · 2026
    Article
  4. Review
  5. 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

10 authors.

Miroslav Dinić *Group for Probiotics and Microbiota-Host Interaction, Department of Microbiology and Plant Biology, Institute of Molecular Genetics and Genetic Engineering, University of Belgrade, Belgrade, Serbia. miroslav.dinic@imgge.bg.ac.rs.
Jelena Đokić *Group for Probiotics and Microbiota-Host Interaction, Department of Microbiology and Plant Biology, Institute of Molecular Genetics and Genetic Engineering, University of Belgrade, Belgrade, Serbia.
Stefan JakovljevićGroup for Probiotics and Microbiota-Host Interaction, Department of Microbiology and Plant Biology, Institute of Molecular Genetics and Genetic Engineering, University of Belgrade, Belgrade, Serbia.
Emilija BrdarićGroup for Probiotics and Microbiota-Host Interaction, Department of Microbiology and Plant Biology, Institute of Molecular Genetics and Genetic Engineering, University of Belgrade, Belgrade, Serbia.
Hristina MitrovićGroup for Probiotics and Microbiota-Host Interaction, Department of Microbiology and Plant Biology, Institute of Molecular Genetics and Genetic Engineering, University of Belgrade, Belgrade, Serbia.
Aleksandar BisenićGroup for Probiotics and Microbiota-Host Interaction, Department of Microbiology and Plant Biology, Institute of Molecular Genetics and Genetic Engineering, University of Belgrade, Belgrade, Serbia.
Dušan RadojevićGroup for Probiotics and Microbiota-Host Interaction, Department of Microbiology and Plant Biology, Institute of Molecular Genetics and Genetic Engineering, University of Belgrade, Belgrade, Serbia.
Svetlana Soković BajićGroup for Probiotics and Microbiota-Host Interaction, Department of Microbiology and Plant Biology, Institute of Molecular Genetics and Genetic Engineering, University of Belgrade, Belgrade, Serbia.
Sergej TomićInstitute for the Application of Nuclear Energy, University of Belgrade, Belgrade, Serbia.
Nataša GolićGroup for Probiotics and Microbiota-Host Interaction, Department of Microbiology and Plant Biology, Institute of Molecular Genetics and Genetic Engineering, University of Belgrade, Belgrade, Serbia.

Funding

Ministry of Science, Technological Development and Innovations of the Republic of Serbia 451-03-136/2025-03/200042Ministry of Science, Technological Development and Innovations of the Republic of Serbia 451-03-66/2024-03/200019Science Fund of the Republic of Serbia 7744507, NextGenBiotics
6 · The paper itself

Abstract

Alterations in the abundance of Bacteroides species are linked to the disruption of the intestinal epithelial barrier and chronic inflammation and has been increasingly recognized as a factor in the development of neurological and neuropsychiatric disorders. Nevertheless, the exact role of Bacteroides species in the gut-brain cross-talk is still largely unexplored. Here, we investigated the immunoregulatory and neuromodulatory potential of two poorly characterized Bacteroides species, including Bacteroides cellulosilyticus and Bacteroides xylanisolvens. The results revealed that both Bacteroides isolates reduced inflammation in Caco-2 intestinal epithelial cells by decreasing the level of IL-8 chemokine and transcription of NF-kB, the two key factors involved in gut inflammation development and barrier disruption. In addition, the Bacteroides strains in the co-culture of Caco-2 cells and phytohemagglutinin-stimulated PBMCs reduced the production of pro-inflammatory cytokines TNF-α and IL-1β, as well as Th1-polarizing IFN-γ cytokine. Finally, in Caenorhabditis elegans, Bacteroides strains differently modulated the expression of the genes implicated in GABA, serotonin and dopamine signaling and synaptic vesicles release pointed to the strain-specific effects of these isolates on neural function. Altogether, these in vitro results show that tested Bacteroides strains may exert anti-inflammatory and neuromodulatory effects, indicating their potential role in microbiota-gut-brain axis.

Indexed as

BacteroidesGastrointestinal MicrobiomeAnimalsCaco-2 CellsCaenorhabditis elegansCoculture TechniquesCytokinesHumansInflammationLeukocytes, MononuclearNF-kappa BCytokinesNF-kappa BBacteroides cellulosilyticusBacteroides xylanisolvensCaenorhabditis elegansGut epithelial barrierNeurotransmittersShort-chain fatty acids

Identifiers

PMID41168250
PMCPMC12575647

What OpenQuestion holds

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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.