Evidence map›Paper›PMID 40691769›Full record

ArticleBMC infectious diseases2025

Determination of the effect of pyocyanin and Saccharomyces boulardii on gut microbiota and TLR4/MyD88/NF-κB and NLRP3 signaling pathways in sepsis induced by cecal ligation and puncture in rats.

Mahmut Ucar, Ozgur Celebi, Demet Celebi, Sumeyye Baser, Mustafa Can Guler, Ayhan Tanyeli, Metin Kılıclıoglu, Ahmet Yılmaz, Serkan Yıldırım

Abstract read
In one paragraph

Article in BMC infectious diseases, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
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

9 authors.

Mahmut UcarDepartment of Medical Microbiology, Atatürk University, Faculty of Medicine, Erzurum, 25240, Turkey.ORCID http://orcid.org/0000-0003-2740-6476
Ozgur CelebiDepartment of Medical Microbiology, Atatürk University, Faculty of Medicine, Erzurum, 25240, Turkey.ORCID http://orcid.org/0000-0003-4578-9474
Demet CelebiDepartment of Microbiology, Atatürk University, Faculty of Veterinary, Erzurum, 25240, Turkey. celebiidil@atauni.edu.tr.ORCID http://orcid.org/0000-0002-2355-0561
Sumeyye BaserDepartment of Pharmaceutical Microbiology, Erzincan Binali Yıldırım University, Faculty of Pharmacy, Erzincan, 24100, Turkey.ORCID http://orcid.org/0000-0003-2391-8191
Mustafa Can GulerDepartment of Physiology, Atatürk University, Faculty of Medicine, Erzurum, 25240, Turkey.ORCID http://orcid.org/0000-0001-8588-1035
Ayhan TanyeliDepartment of Physiology, Atatürk University, Faculty of Medicine, Erzurum, 25240, Turkey.ORCID http://orcid.org/0000-0002-0095-0917
Metin KılıclıogluDepartment of Pathology, Atatürk University, Faculty of Veterinary, Erzurum, 25240, Turkey.ORCID http://orcid.org/0000-0001-9055-2164
Ahmet YılmazAtatürk University, Vocational School of Health Services, Erzurum, 25240, Turkey.ORCID http://orcid.org/0000-0002-2350-1516
Serkan YıldırımDepartment of Pathology, Atatürk University, Faculty of Veterinary, Erzurum, 25240, Turkey.ORCID http://orcid.org/0000-0003-2457-3367

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sepsis is a life-threatening systemic inflammatory condition marked by a dysregulated host response to infection. The intestinal microbiota plays a pivotal role in maintaining immune homeostasis and epithelial barrier integrity, whereas dysbiosis significantly contributes to the pathogenesis of sepsis. This study investigates the effects of the Pseudomonas aeruginosa-derived metabolite Pyocyanin and the probiotic Saccharomyces boulardii (S. boulardii) on microbial composition and the TLR4/MyD88/NF-κB/NLRP3 signaling axis in a cecal ligation and puncture (CLP)-induced rat model of sepsis. The experimental design assessed the synergistic or antagonistic effects of single and combined treatments using molecular, microbiome, and immunohistochemical parameters to evaluate histopathological damage and microbial ecological dynamics. Seven experimental groups were established following CLP. Intra-abdominal Pyocyanin (10 nmol/g) and oral probiotic (10⁶ CFU/kg) treatments were administered either individually or in combination. Focused Ion Beam - Scanning Electron Microscopy (FIB-SEM) analyses revealed that the amorphous structure of Pyocyanin interacted with the surface of S. boulardii. Western blot analysis showed a 2.3-fold increase in TLR4/NF-κB expression in the CLP group (p ≤ 0.05), which synergistically rose to 4.5-fold with Pyocyanin (p ≤ 0.001), whereas probiotic treatment decreased expression levels by 35%. According to 16 S rRNA sequencing, Pyocyanin reduced α-diversity by increasing Lactobacillaceae abundance to 32.66% (Shannon index: 3.598 vs. 4.433 in control), while S. boulardii enhanced β-diversity by elevating Coriobacteriaceae (5.85%) and Prevotellaceae (10.63%) levels (Tables 2, 3 and 4). PCoA confirmed 41.7% Bray-Curtis dissimilarity between groups at the species level (PERMANOVA R²=0.38, p = 0.002). Histopathologically, severe hepatocyte necrosis (73.2 ± 6.1%, p = 0.0022) and a 4.2-fold increase in hepatic TGF-β expression were observed in the CLP group, whereas epithelial barrier damage was significantly attenuated in the probiotic groups. Immunofluorescence analysis revealed that combined treatment reduced Caspase-8 and TLR4 expression by 28% compared to Pyocyanin alone (p ≤ 0.05). In conclusion, S. boulardii supported microbiota homeostasis by suppressing TLR4/NF-κB signaling, whereas Pyocyanin exacerbated the inflammatory response via NLRP3 activation. These findings provide molecular evidence supporting probiotic-assisted immunomodulatory strategies in sepsis therapy.

Indexed as

Carrier ProteinsGastrointestinal MicrobiomeProbioticsPyocyanineSaccharomyces boulardiiSepsisSignal TransductionAnimalsCecumDisease Models, AnimalLigationMaleMyeloid Differentiation Factor 88NF-kappa BNLR Family, Pyrin Domain-Containing 3 ProteinRatsCarrier ProteinsMyd88 protein, ratMyeloid Differentiation Factor 88NF-kappa BNLR Family, Pyrin Domain-Containing 3 ProteinNlrp3 protein, ratPyocyanineTlr4 protein, ratToll-Like Receptor 4Gut microbiotaPyocyaninSaccharomyces boulardiiSepsisWestern blot

Identifiers

PMID40691769
PMCPMC12281731

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.