Novel Antibiofilm Approach Using Bioactive Glasses F18 and 45S5 Against Clinical Isolates of Staphylococcus aureus in Chronic Rhinosinusitis
Authors:
- João Vitor Bizinoto CaetanoJCJoão Vitor Bizinoto Caetano
- Maria Clara Antunes AlvesMAMaria Clara Antunes Alves
- Marina Zilio FantucciMarina Zilio Fantucci
- Lilian Eslaine Costa Mendes da SilvaLilian Eslaine Costa Mendes da Silva
- Denny Marcos GarciaDenny Marcos Garcia
- Marina Trevelin SouzaMarina Trevelin Souza
- Rafael Soares StenicoRSRafael Soares Stenico
- Márcia Andreia Mesquita Silva da VeigaMárcia Andreia Mesquita Silva da Veiga
- Wilma Terezinha Anselmo‐LimaWilma Terezinha Anselmo‐Lima
- Fabiana Cardoso Pereira ValeraFabiana Cardoso Pereira Valera
- Edwin TamashiroEdwin Tamashiro
Open Access
- 15 May 2026
- journal article
- Published by Wiley in Journal of Biomedical Materials Research Part A
- Vol. 114 (5) , e70082
Abstract
S. aureus plays a central role in chronic rhinosinusitis (CRS), contributing to acute exacerbations and persistent infections through biofilm formation. With rising antibiotic resistance, bioactive glasses such as F18 and 45S5 have emerged as potential alternative antimicrobial agents. To evaluate the antimicrobial effects of F18 and 45S5 on S. aureus isolates from CRS patients, focusing on planktonic growth, biofilm formation, and mechanisms of action. Clinical S. aureus isolates were exposed to F18 and 45S5 (0–512 μg/mL) using a modified Calgary Biofilm Device. Biofilm biomass was quantified by crystal violet staining and spectrophotometry. A pH‐controlled assay was performed to determine whether alkalinization mediated antibiofilm effects. Inductively coupled plasma analysis characterized F18 ion‐release kinetics. Expression of biofilm‐related genes (icaA, icaB, icaD, agrA, agrC) was quantified, and biofilm morphology was examined by scanning electron microscopy. Both bioglasses inhibited biofilm formation at concentrations ≥ 128 μg/mL but did not eradicate mature biofilms. At 512 μg/mL, F18 and 45S5 reduced the biofilm optical density by 78% and 67%, respectively. Although pH elevation occurred, biofilm inhibition was independent of pH variation. F18 exposure downregulated ica operon genes but not agr genes. Ion analysis demonstrated concentration‐dependent release of Ca and Si, with no evidence of apatite formation. SEM showed reduced extracellular matrix and altered bacterial organization. F18 and 45S5 inhibit S. aureus biofilm formation through pH‐independent mechanisms associated with ion release and suppression of matrix‐related genes, supporting their potential as adjunctive strategies in CRS management.Keywords
Funding Information
- Fundação de Amparo à Pesquisa do Estado de São Paulo (2019/05843‐2)
- Fundação de Amparo à Pesquisa do Estado de São Paulo (2013/07793‐6)
- Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (001)
- Fundação de Apoio ao Ensino, Pesquisa e Assistência
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