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Submitted: 24 Nov 2025
Revision: 13 Feb 2026
Accepted: 15 Feb 2026
ePublished: 26 Sep 2026
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J Iran Dent Assoc. 2026;38(3-4): 72-81.
doi: 10.34172/jida.2303
  Abstract View: 117100
  PDF Download: 57711

Original Article

Effect of Selenium Nanoparticles on Streptococcus Mutans Biofilm Gene Expression Using Real Time PCR

Niyousha Noorullahi ORCID logo, Farid Abbasi ORCID logo, Aliye Sehatpour* ORCID logo, Ronak Bakhtiari ORCID logo
*Corresponding Author: Email: a.sehhat@shahed.ac.ir

Abstract

Background: Streptococcus mutans is one of the main causes of dental caries. Although several nanoparticles have been investigated as antimicrobial agents, the antibiofilm potential and mechanistic action of biosynthesized selenium nanoparticles (SeNPs) remain insufficiently characterized. This study aimed to test the hypothesis that biosynthesized SeNPs inhibit S. mutans growth and biofilm formation through downregulation of the biofilm-associated gtfB gene.

Methods: SeNPs were biosynthesized using Artemisia scoparia extract and characterized for nanoscale morphology. Their antibacterial activity against S. mutans was assessed using standard in vitro susceptibility assays, while antibiofilm effects were evaluated using biofilm detection methods. The impact of SeNPs exposure on gtfB gene expression was analyzed by RT-PCR and compared with untreated controls.

Results: The biosynthesized SeNPs demonstrated significant antibacterial activity against S. mutans and induced a reduction in biofilm-associated phenotypic characteristics. Gene expression analysis revealed significant downregulation of gtfB expression in treated samples compared with untreated controls.

Conclusion: Within the limitations of an in vitro model, biosynthesized SeNPs demonstrated antibacterial and antibiofilm activity against S. mutans, likely mediated through inhibition of gtfB expression. These findings suggest that SeNPs may serve as a promising adjunctive strategy for controlling cariogenic biofilms. However, further in vivo studies and comparative evaluations with existing antimicrobial agents are required to establish clinical relevance.

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