Ions released from a S-PRG filler induces oxidative stress in Candida albicans inhibiting its growth and pathogenicity
Open accessAbstract
Candida albicans causes opportunistic fungal infections usually hidden among more dominant bacteria and does not exhibit high pathogenicity in vivo. Among the elderly, due to reduced host resistance to pathogens attributable to immunoscenesence, oral candidiasis is more likely to develop often leading to systemic candidiasis. Surface pre-reacted glass ionomer filler (S-PRG filler) is an ion-releasing functional bioactive glass that can release and recharge six ions which in turn strengthens tooth structure, inhibits demineralization arising from dental caries, and suppresses dental plaque accumulation. However, its effects on C. albicans have never been elucidated. Here, we evaluated the effects of ion released from S-PRG filler on C. albicans. Results show that extraction liquids containing released ions (ELIS) decreased the amount of hydrogen peroxide and catalase activity in C. albicans. Moreover, ELIS presence was found to affect C. albicans: (1) suppression of fungal growth and biofilm formation, (2) prevent adherence to denture base resin, (3) inhibit dimorphism conversion, and (4) hinder the capability to produce secreted aspartyl proteinase. Taken together, our findings suggest that ELIS induces oxidative stress in C. albicans and suppresses its growth and pathogenicity. In this regard, we propose that ELIS has the potential to be clinically used to help prevent the onset and inhibition of oral candidiasis among the elderly population.
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Increases in ROS levels could explain the observed fungicidal activity against planktonic and biofilm C. auris.
“These increases in ROS levels could explain the observed fungicidal activity against planktonic and biofilms of C. auris as previously demonstrated in other studies [57–59].”
From Aprepitant, an antiemetic agent, interferes with metal ion homeostasis of<i>Candida auris</i>and displays potent synergistic interactions with azole drugs (2020) · cites this paper as [59]
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References 38 · Cited by 37
- Authors
- Tamura, M., Cueno, M. E., Abe, K., Kamio, N., Ochiai, K., & Imai, K.
- Affiliations
- Nihon University (JP)
- Corresponding author
- Tamura, Muneaki
- Venue
- Cell Stress and Chaperones
- Publisher
- Elsevier BV
- Published
- 2018-11
- Volume
- 23
- Issue
- 6
- Pages
- 1337-1343
- ISSN
- 1355-8145 (ISSN-L)
- PMC
- PMC6237688
- OpenAlex
- W2805527156
- Cited by
- 37
- References
- 38
- Citations by year
- 2026: 4 · 2025: 5 · 2024: 3 · 2023: 4 · 2022: 8 · 2021: 9 · 2020: 3 · 2019: 1
- FWCI
- 2.46
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Cell Stress and Chaperones (publishedVersion, cc-by-nc-nd)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Japan Society for the Promotion of Science (24593168 and 15K11456)
- Topics
- Health Sciences › Medicine › Infectious Diseases › Antifungal resistance and susceptibility
- Health Sciences › Dentistry › Orthodontics › Dental materials and restorations
- Health Sciences › Dentistry › Oral Surgery › Endodontics and Root Canal Treatments
- Keywords
- Candida albicans, oxidative stress, oral candidiasis, fungal growth inhibition, biofilm formation, secreted aspartyl proteinases, hydrogen peroxide, catalase activity, immunosenescence
- MeSH terms
- Acrylic Resins, Aged, Candida albicans, Candidiasis, Oral, Catalase, Cell Adhesion, Denture Bases, Glass Ionomer Cements, Humans, Ions, Silicon Dioxide, Oxidative Stress, Biofilms, Aspartic Acid Proteases
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