{"title":"Efficacy of gigantol, a bibenzyl compound, against <i>Porphyromonas gingivalis</i>.","authors":"Arthit Klaophimai, Nattanon Kosulwat, Thongtos Saeghueng, Tanadon Sirijaruworn, Bunyawat Ua-Arak, Sucharat Sanongkiet, Sirinthip Klaophimai, Pongsak Utaisincharoen, Matsayapan Pudla","doi":"10.1080/20002297.2025.2525234","DOIUrl":null,"url":null,"abstract":"<p><strong>Aim: </strong>This study aims to investigate the inhibitory effect of gigantol against <i>P. gingivalis</i>.</p><p><strong>Materials and methods: </strong>The effect of gigantol against the planktonic culture of <i>P. gingivalis</i> was determined by broth microdilution and CFU assay. In addition, bacterial cell surface hydrophobicity and aggregation were elucidated. Confocal laser scanning microscopy (CLSM) and scanning electron microscopy (SEM) were performed to observe biofilm thickness and the biofilm structure, respectively. The gingipain-related genes were evaluated using qPCR. Moreover, molecular docking analysis has also detected the interaction between gigantol and gingipains. Finally, the cytotoxicity effect of gigantol on human gingival fibroblasts (HGFs) was also observed by MTT assay.</p><p><strong>Results: </strong>The MIC and MBC of gigantol against planktonic <i>P. gingivalis</i> were 0.312 mg/mL. The findings indicated that the effect of gigantol at sub-MIC concentrations can also suppress bacterial growth. Additionally, this compound increased cell surface hydrophobicity and aggregation. CLSM images demonstrated its inhibitory effect on the pre-formed biofilm of <i>P. gingivalis</i>. SEM exhibited that gigantol could affect the bacterial membrane. The downregulation of gingipain-related gene expression was observed. Moreover, molecular docking showed that this compound blocks Kpg and RgpB proteases. Furthermore, the cytotoxicity of gigantol on HGFs exhibited less toxicity than 0.12% CHX.</p><p><strong>Conclusion: </strong>Our findings indicated that gigantol inhibits the <i>P. gingivalis</i> biofilm and establishment, which may lead to a potential therapeutic compound for periodontitis patients.</p>","PeriodicalId":16598,"journal":{"name":"Journal of Oral Microbiology","volume":"17 1","pages":"2525234"},"PeriodicalIF":3.7000,"publicationDate":"2025-06-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12203691/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Oral Microbiology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1080/20002297.2025.2525234","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/1 0:00:00","PubModel":"eCollection","JCR":"Q2","JCRName":"MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Aim: This study aims to investigate the inhibitory effect of gigantol against P. gingivalis.
Materials and methods: The effect of gigantol against the planktonic culture of P. gingivalis was determined by broth microdilution and CFU assay. In addition, bacterial cell surface hydrophobicity and aggregation were elucidated. Confocal laser scanning microscopy (CLSM) and scanning electron microscopy (SEM) were performed to observe biofilm thickness and the biofilm structure, respectively. The gingipain-related genes were evaluated using qPCR. Moreover, molecular docking analysis has also detected the interaction between gigantol and gingipains. Finally, the cytotoxicity effect of gigantol on human gingival fibroblasts (HGFs) was also observed by MTT assay.
Results: The MIC and MBC of gigantol against planktonic P. gingivalis were 0.312 mg/mL. The findings indicated that the effect of gigantol at sub-MIC concentrations can also suppress bacterial growth. Additionally, this compound increased cell surface hydrophobicity and aggregation. CLSM images demonstrated its inhibitory effect on the pre-formed biofilm of P. gingivalis. SEM exhibited that gigantol could affect the bacterial membrane. The downregulation of gingipain-related gene expression was observed. Moreover, molecular docking showed that this compound blocks Kpg and RgpB proteases. Furthermore, the cytotoxicity of gigantol on HGFs exhibited less toxicity than 0.12% CHX.
Conclusion: Our findings indicated that gigantol inhibits the P. gingivalis biofilm and establishment, which may lead to a potential therapeutic compound for periodontitis patients.
期刊介绍:
As the first Open Access journal in its field, the Journal of Oral Microbiology aims to be an influential source of knowledge on the aetiological agents behind oral infectious diseases. The journal is an international forum for original research on all aspects of ''oral health''. Articles which seek to understand ''oral health'' through exploration of the pathogenesis, virulence, host-parasite interactions, and immunology of oral infections are of particular interest. However, the journal also welcomes work that addresses the global agenda of oral infectious diseases and articles that present new strategies for treatment and prevention or improvements to existing strategies.
Topics: ''oral health'', microbiome, genomics, host-pathogen interactions, oral infections, aetiologic agents, pathogenesis, molecular microbiology systemic diseases, ecology/environmental microbiology, treatment, diagnostics, epidemiology, basic oral microbiology, and taxonomy/systematics.
Article types: original articles, notes, review articles, mini-reviews and commentaries