Evidence map›Paper›PMID 39755609›Full record

ArticleBMC oral health2025

Cordycepin affects Streptococcus mutans biofilm and interferes with its metabolism.

Yidan Shao, Wenyan Zhu, Shanshan Liu, Kai Zhang, Yu Sun, Yudong Liu, Tingchi Wen, Yingxue Zou, Qingwei Zheng

Abstract read
In one paragraph

Article in BMC oral health, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Multifaceted roles ofFrontiers in cellular and infection microbiology · 2025
    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.

Yidan ShaoAnhui Key Laboratory of Infection and Immunity, Bengbu Medical University, 2600 Dong Hai Avenue, Bengbu, 233030, China.
Wenyan ZhuAnhui Key Laboratory of Infection and Immunity, Bengbu Medical University, 2600 Dong Hai Avenue, Bengbu, 233030, China.
Shanshan LiuAnhui Key Laboratory of Infection and Immunity, Bengbu Medical University, 2600 Dong Hai Avenue, Bengbu, 233030, China.
Kai ZhangDepartment of Stomatology, The First Affiliated Hospital of Bengbu Medical University, 287 Chuang Huai Road, Bengbu, 233004, China.
Yu SunDepartment of Biochemistry and Molecular Biology, Bengbu Medical University, 2600 Dong Hai Avenue, Bengbu, 233030, China.
Yudong LiuAnhui Key Laboratory of Infection and Immunity, Bengbu Medical University, 2600 Dong Hai Avenue, Bengbu, 233030, China.
Tingchi WenThe Engineering Research Center of Southwest Bio-Pharmaceutical Resources, Ministry of Education, Guizhou University, Guiyang, 550025, China.
Yingxue ZouAcademy of Medical Engineering and Transform Medicine, Tianjin University, No.92 Weijin Road, Nankai District, Tianjin, 300072, China. yingxuezou@163.com.
Qingwei ZhengAcademy of Medical Engineering and Transform Medicine, Tianjin University, No.92 Weijin Road, Nankai District, Tianjin, 300072, China. bio_zqw@bbmu.edu.cn.

Funding

Key Science Research Project Funding of Education Department of Anhui Province KJ2020A0574the First Affiliated Hospital of Bengbu Medical College Science Fund for Outstanding Young Scholars 2019byyfyyq07the University Synergy Innovation Program of Anhui Province GXXT-2021-056
6 · The paper itself

Abstract

backgroundStreptococcus mutans (S. mutans) contributes to caries. The biofilm formed by S. mutans exhibits greater resistance to drugs and host immune defenses than the planktonic form of the bacteria. The objective of this study was to evaluate the anti-biofilm effect of cordycepin from the perspective of metabolomics.

methodsThe minimum inhibitory concentration (MIC) was determined to evaluate the antimicrobial effect of cordycepin on planktonic S. mutans. The 24-h biofilm was treated with 128 µg/mL of cordycepin for 10 min at the 8- or 20-h time points. Biofilm biomass and metabolism were assessed using crystal violet and MTT assays and cordycepin cytotoxicity was evaluated in human oral keratinocytes (HOK) using CCK-8 assays. The live bacterial rate and the biofilm volume were assessed by confocal laser scanning microscopy. Metabolic changes in the biofilm collected at different times during with cordycepin were analyzed by metabolomics and verified by quantitative real-time PCR.

resultsThe results showed that treatment with 128 µg/mL cordycepin reduced both the biomass and metabolic activity of the biofilm without killing the bacteria, and cordycepin at this concentration showed good biocompatibility. Metabolomics analysis showed that differentially abundant metabolites following cordycepin treatment were mainly related to purine and nucleotide metabolism. After immediate treatment with cordycepin, genes related to purine and nucleotide metabolism were downregulated, and the levels of various metabolites changed significantly. However, the effect was reversible. After continuing culture for 4 h, the changes in genes and most metabolites were reversed, although the levels of 2'-deoxyadenosine, 2'-deoxyinosine, and adenine remained significantly different.

conclusionsCordycepin has the effect of anti-biofilm of S. mutans, mainly related to purine and nucleotide metabolism.

Indexed as

BiofilmsDeoxyadenosinesMicrobial Sensitivity TestsStreptococcus mutansAnti-Bacterial AgentsBiomassHumansKeratinocytesMetabolomicsMicroscopy, ConfocalReal-Time Polymerase Chain ReactionTetrazolium SaltsAnti-Bacterial AgentscordycepinDeoxyadenosinesTetrazolium SaltsBiofilmCordycepinMetabolomicStreptococcus mutans

Identifiers

PMID39755609
PMCPMC11700466

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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.