# Suppressive Effects of Kouboku on Methyl Mercaptan Production and Biofilm Formation in Porphyromonas gingivalis

**Authors:** Yuri Taniguchi, Kazuhisa Ouhara, Yoko Sato, Mikio Shoji, Yitong Hou, Ruoqi Zhai, Ryousuke Fujimori, Naoya Kuwahara, Tetsuya Tamura, Shinji Matsuda, Noriyoshi Mizuno

PMC · DOI: 10.1111/omi.12493 · Molecular Oral Microbiology · 2025-02-27

## TL;DR

This study shows that Kouboku, a Chinese herbal medicine, can reduce harmful methyl mercaptan production and biofilm formation in a bacteria linked to gum disease.

## Contribution

The study reveals Kouboku's ability to inhibit P. gingivalis biofilm and adhesion, and enhance antibiotic effectiveness.

## Key findings

- Kouboku inhibited biofilm formation in P. gingivalis and Fusobacterium nucleatum co-cultures.
- Kouboku reduced P. gingivalis adhesion to epithelial cells by downregulating fimA expression.
- Honokiol and magnolol from Kouboku lowered the MICs of several antibiotics against P. gingivalis.

## Abstract

Porphyromonas gingivalis, the bacterium responsible for periodontitis, produces several pathogenic factors, including methyl mercaptan, which contribute to the disease. Kouboku (Magnoliaceae), a Chinese herbal medicine, has been shown to suppress methyl mercaptan production from P. gingivalis. In this study, we investigated the inhibitory effect of Kouboku on methyl mercaptan production, biofilm formation, P. gingivalis‐host cell interactions, and its potential synergistic antibacterial effect with antibiotics. Five standard and five clinically isolated P. gingivalis strains were evaluated. Methyl mercaptan production was measured using OralChroma. The mRNA expression of mgl and fimA, which are involved in methyl mercaptan synthesis and adhesion molecules, was assessed using quantitative PCR. Biofilm formation by P. gingivalis and epithelial cell adhesion were analyzed following treatment with or without Kouboku. Furthermore, the effects of the active ingredients of Kouboku, honokiol, and magnolol, on the minimum inhibitory concentrations (MICs) of antibiotics against P. gingivalis were determined. No significant differences were observed in the suppression of methyl mercaptan production among P. gingivalis strains with different FimA genotypes treated with Kouboku. Moreover, Kouboku inhibited biofilm formation in co‐cultures of P. gingivalis and Fusobacterium nucleatum, as well as the adhesion of P. gingivalis to gingival epithelial cells through the downregulation of fimA. Treatment with honokiol and magnolol reduced the MICs of ampicillin, gentamicin, erythromycin, and tetracycline against P. gingivalis. These findings demonstrate that Kouboku affects P. gingivalis by modulating its adhesion to other bacteria and host cells, and enhances the antibacterial activity of certain antibiotics.

## Linked entities

- **Genes:** CLEC10A (C-type lectin domain containing 10A) [NCBI Gene 10462], fimA (major type 1 subunit fimbrin) [NCBI Gene 913688]
- **Chemicals:** methyl mercaptan (PubChem CID 878), honokiol (PubChem CID 72303), magnolol (PubChem CID 72300), ampicillin (PubChem CID 6249), gentamicin (PubChem CID 3467), erythromycin (PubChem CID 12560), tetracycline (PubChem CID 54675776)
- **Diseases:** periodontitis (MONDO:0005076)
- **Species:** Porphyromonas gingivalis (taxon 837), Fusobacterium nucleatum (taxon 851), Mus musculus (taxon 10090)

## Full-text entities

- **Diseases:** periodontitis (MESH:D010518)
- **Species:** Porphyromonas gingivalis (species) [taxon 837], Fusobacterium nucleatum (species) [taxon 851]

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12000855/full.md

## References

30 references — full list in the complete paper: https://tomesphere.com/paper/PMC12000855/full.md

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Source: https://tomesphere.com/paper/PMC12000855