Evidence map›Paper›PMID 41938865›Full record

ArticleFrontiers in cellular and infection microbiology2026

Polydatin as a natural ClpP modulator for combating methicillin-resistant

Ying Qin, Jingjing Yang, Guangming Wang, Luna Yang, Dacheng Wang, Yongxin Luan

Abstract read
In one paragraph

Article in Frontiers in cellular and infection microbiology, 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
–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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

6 authors.

Ying Qin *Department of Neurosurgery, First Hospital of Jilin University, Changchun, China.
Jingjing Yang *College of Animal Science, Jilin University, Changchun, China.
Guangming WangDepartment of Neurosurgery, First Hospital of Jilin University, Changchun, China.
Luna YangDepartment of Pharmacology, College of Basic Medical Sciences, Jilin University, Changchun, China.
Dacheng WangCollege of Animal Science, Jilin University, Changchun, China.
Yongxin LuanDepartment of Neurosurgery, First Hospital of Jilin University, Changchun, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Methicillin resistant Methods: ClpP inhibitory activity was evaluated by enzymatic assay. The effects of polydatin on bacterial growth, hemolytic activity, virulence gene expression, adhesion to fibrinogen, and host cell invasion were assessed Results: Polydatin showed limited antibacterial activity but significantly inhibited ClpP and reduced the expression of key virulence factors, including Hla, PVL, and RNAIII. It also impaired bacterial adhesion to fibrinogen and invasion of host cells. Binding studies supported the interaction between polydatin and ClpP. Discussion: Polydatin attenuates MRSA pathogenicity by targeting ClpP associated virulence regulation rather than bacterial viability. These findings identify polydatin as a promising antivirulence candidate and provide a basis for developing alternative therapeutic strategies against MRSA infections.

Indexed as

Anti-Bacterial AgentsEndopeptidase ClpGlucosidesMethicillin-Resistant Staphylococcus aureusStaphylococcal InfectionsStilbenesAnimalsBacterial AdhesionDisease Models, AnimalFallopia japonicaFemaleHumansMicePneumonia, StaphylococcalVirulenceVirulence FactorsAnti-Bacterial AgentsEndopeptidase ClpGlucosidespolydatinStilbenesVirulence Factorsantibiotic resistancecaseinolytic protease P (ClpP)hemolysis inhibitionmethicillin-resistant Staphylococcus aureus (MRSA)pneumonia modelpolydatin

Identifiers

PMID41938865
PMCPMC13044082

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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.