Abstract :
Bacterial wilt caused by Ralstonia solanacearum remains one of the most destructive constraints in tomato production worldwide. The pathogen’s virulence is tightly regulated by quorum sensing (QS), which controls exopolysaccharide (EPS) biosynthesis, extracellular enzyme secretion, and biofilm formation. Targeting QS through quorum quenching (QQ) represents a promising anti-virulence strategy without imposing the selective pressure associated with conventional bactericides. This study investigated the dual role of potassium silicate as (i) a QS-interfering agent that modulates bacterial virulence traits and (ii) an inducer of host systemic resistance. Potassium silicate at 1 mM significantly reduced EPS production and biofilm formation, whereas 2 mM enhanced peroxidase activity in tomato plants. Disease severity was reduced during the early stages of infection in silica-treated plants. These findings indicate that potassium silicate attenuates bacterial wilt development through the integrated modulation of pathogen virulence and host defense responses. This study provides mechanistic insight into silicon-mediated plant protection and highlights potassium silicate as a sustainable strategy for bacterial wilt management.
Keywords :
Bacterial wilt, quorum quenching., quorum sensing, Silicon-Mediated Resistance, Tomato ImmunityReferences :
- D’Aquila, P., De Rose, E., Sena, G., Scorza, A., Cretella, B., Passarino, G., & Bellizzi, D. (2024). Quorum Quenching Approaches against Bacterial-Biofilm-Induced Antibiotic Resistance. Antibiotics, 13(7), 1–26. https://doi.org/10.3390/antibiotics13070619
- Hawerroth, C., Araujo, L., Bermúdez-Cardona, M. B., Silveira, P. R., Wordell Filho, J. A., & Rodrigues, F. A. (2019). Silicon-mediated maize resistance to macrospora leaf spot. Tropical Plant Pathology, 44(2), 192–196. https://doi.org/10.1007/s40858-018-0247-8
- Huang, J., Wang, R., Zhang, Q., Wang, C., Liang, T., Hikichi, Y., Ohnishi, K., Jiang, G., Guo, T., & Zhang, Y. (2023). Positive regulation of the PhcB neighbouring regulator PrhX on expression of the type III secretion system and pathogenesis in Ralstonia solanacearum. Molecular Plant Pathology, (July), 1–13. https://doi.org/10.1111/mpp.13398
- Jiang, N., Wang, L., Gao, Y., Lin, W., & Cai, K. (2019). Transcriptome Analysis Reveals New Insights into the Silicon-Induced Bacterial Wilt Resistance in Tomato (Solanum lycopersicum L.). International Journal of Molecular Sciences, 20(4), 904. https://pmc.ncbi.nlm.nih.gov/articles/PMC6387441/
- Jinli, Y., Peng, L., Xiaoqing, W., Minya, Z., Hongyu, S., Guohui, Y., Xuemei, C., Huishan, W., Xiaofan, Z., Lisheng, L., & Lianhui, Z. (2022). RasI/R Quorum Sensing System Controls the Virulence of Ralstonia solanacearum Strain EP1. Applied and Environmental Microbiology, 88(15), e00325-22. https://doi.org/10.1128/aem.00325-22
- Kumar, J. S., Umesha, S., Prasad, K. S., & Niranjana, P. (2016). Detection of Quorum Sensing Molecules and Biofilm Formation in Ralstonia solanacearum. Current Microbiology, 72(3), 297–305. https://doi.org/10.1007/s00284-015-0953-0
- Lijon, M. B., Matsu-ura, Y., Ukita, T., Arakawa, K., & Miyamoto, T. (2025). Identification and Characterization of Antiyeast Organic Acids Produced by Lactiplantibacillus plantarum 3121M0s Derived from Mongolian Traditional Fermented Milk, Airag. Microorganisms, 13(9). https://doi.org/10.3390/microorganisms13092017
- Milling, A., Babujee, L., & Allen, C. (2011). Ralstonia solanacearum extracellular polysaccharide is a specific elicitor of defense responses in wilt-resistant tomato plants. PLoS ONE, 6(1). https://doi.org/10.1371/journal.pone.0015853
- Pereira, L. S. (2024). Silicon, An Emergent Strategy to Lighten the Effects of (A)Biotic Stresses on Crops: A Review. Journal of Agronomy and Crop Science, 210(6), e12762. https://onlinelibrary.wiley.com/doi/10.1111/jac.12762
- Santos, C. dos, & Franco, O. L. (2023). Pathogenesis-Related Proteins (PRs) with Enzyme Activity in Plant Defense: Peroxidase, Chitinase, and Ribonuclease. Encyclopedia, 3(3), 958–972.
- Shannon, L. M., Kay, E., & Lew, J. Y. (1966). Peroxidase Isozymes from Horseradish Roots: I. Isolation and Physical Properties. Journal of Biological Chemistry, 241(9), 2166–2172. https://www.jbc.org
- Spratt, M. R., & Lane, K. (2022). Navigating Environmental Transitions: the Role of Phenotypic Variation in Bacterial Responses. In J. Yount (Ed.), mBio (Vol. 13, Number 6). American Society for Microbiology. https://doi.org/10.1128/mbio.02212-22
- Tsumori, C., Matsuo, S., Murai, Y., & Kai, K. (2022). Quorum Sensing-Dependent Invasion of Ralstonia solanacearum into Fusarium oxysporum Chlamydospores. Microbiology Spectrum, 11(4), 00036–23. https://doi.org/10.1128/spectrum.00036-23
- Verma, K. K., Song, X. P., Liang, Q., Huang, H. R., Bhatt, R., Xu, L., Chen, G. L., & Li, Y. R. (2024). Unlocking the role of silicon against biotic stress in plants. Frontiers in Plant Science, 15, 1–12. https://doi.org/10.3389/fpls.2024.1430804
- Wang, L., Gao, Y., Jiang, N., Yan, J., Lin, W., & Cai, K. (2022). Silicon Controls Bacterial Wilt Disease in Tomato Plants and Inhibits the Virulence-Related Gene Expression of Ralstonia solanacearum. International Journal of Molecular Sciences, 23(13). https://doi.org/10.3390/ijms23136965
- Yang, L., Wei, Z., Li, S., Xiao, R., Xu, Q., Ran, Y., & Ding, W. (2021). Plant secondary metabolite , daphnetin reduces extracellular polysaccharides production and virulence factors of Ralstonia solanacearum. Pesticide Biochemistry and Physiology, (August), 104948. https://doi.org/10.1016/j.pestbp.2021.104948
- Yi, L., Dong, X., Grenier, D., Wang, K., & Wang, Y. (2021). Research progress of bacterial quorum sensing receptors: Classification, structure, function and characteristics. Science of the Total Environment, 763(1). https://doi.org/10.1016/j.scitotenv.2020.143031
- Youmbi, D. Y., Eke, P., Kouokap, L. R. K., Dinango, V. N., Tamghe, G. G., Wakam, L., & Boyom, F. (2022). Endophytic bacteria from Euphorbia antiquorum L. protect Solanum lycopersicum L. against bacterial wilt caused by Ralstonia solanacearum. Egyptian Journal of Biological Pest Control, 32(77), 1–13. https://doi.org/10.1186/s41938-022-00575-x

