In vitro inhibitory effect of statins on planktonic cells and biofilms of the Sporothrix schenckii species complex
Abstract
Introduction. Sporotrichosis, caused by species of the Sporothrix schenckii complex, is the most prevalent subcutaneous mycosis in many areas of Latin America. Statins are a class of drugs widely used for lowering high sterol levels through their action on 3-hydroxy-3-methylglutaryl-CoA reductase, a key enzyme in the synthesis of sterol. Aim. In this study, the antifungal activity of statins (simvastatin, atorvastatin, pravastatin) against planktonic cells and biofilms of S. schenckii complex species was evaluated, as well as the interaction of pravastatin with classical antifungals (amphotericin B, itraconazole, terbinafine). Methodology. Eighteen strains of Sporothrix species were used. The antifungal susceptibility assay was performed using the broth microdilution method. Mature biofilms were exposed to statins and metabolic activity was measured by the XTT reduction assay. Results. MICs of statins ranged from 8 to 512 μg ml−1 and from 8 to 256 μg ml−1 for filamentous and yeast forms, respectively. Regarding mature biofilms, MICs of 50 % inhibition (SMIC50) were 128 μg ml−1 for simvastatin and atorvastatin and >2048 μg ml−1 for pravastatin. MICs of 90 % inhibition (SMIC90) were 512 μg ml−1 for simvastatin and >2048 μg ml−1 for atorvastatin and pravastatin. Conclusion. These results highlight the antifungal and antibiofilm potential of statins against S. schenckii complex species.
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Statins exhibit a broad spectrum of biological activities, including antimicrobial, antiparasitic, antibacterial, antiviral, and antifungal potential.
“Moreover, statins exhibit a broad spectrum of biological activities, including antimicrobial, antiparasitic, antibacterial, antiviral, and antifungal potential [110, 111, 112, 113].”
From Statins as Antifungal Agents: A Review on Drug Repurposing and Nanotechnology-Driven Delivery Strategies (2025) · cites this paper as [113]
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- Authors
- Brilhante, R. S. N., Fonseca, X. M. Q. C., Pereira, V. S., Araújo, G. D. S., Oliveira, J. S. D., Garcia, L. G. S., Rodrigues, A. M., Camargo, Z. P. D., Pereira-Neto, W. A., Castelo-Branco, D. D. S. C. M., Cordeiro, R. D. A., Sidrim, J. J. C., & Rocha, M. F. G.
- Affiliations
- Universidade Federal do Ceará (BR)
- Universidade Estadual do Ceará (BR)
- Universidade Federal de São Paulo (BR)
- Cellular Biology Division, Department of Microbiology, Immunology and Parasitology, Federal University of São Paulo, Sao Paulo, São Paulo, 04023-062, Brazil
- Specialized Center in Medical Mycology, Postgraduate Program in Medical Microbiology, Department of Pathology and Forensic Medicine, Federal University of Ceará, Fortaleza, Ceará, 60430-275, Brazil
- ORCID
- Venue
- Journal of Medical Microbiology
- Publisher
- Microbiology Society
- Published
- 2020-06-01
- Volume
- 69
- Issue
- 6
- Pages
- 838-843
- ISSN
- 0022-2615 (ISSN-L)
- 1473-5644
- OpenAlex
- W3028310048
- Cited by
- 5
- References
- 25
- Citations by year
- 2026: 1 · 2025: 1 · 2024: 1 · 2023: 2
- FWCI
- 0.07
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Journal of Medical Microbiology (publishedVersion)
- PubMed (publishedVersion)
- Funders
- CNPq (305024/2017-5)
- Topics
- Health Sciences › Medicine › Infectious Diseases › Antifungal resistance and susceptibility
- Health Sciences › Medicine › Epidemiology › Fungal Infections and Studies
- Health Sciences › Medicine › Microbiology › Actinomycetales infections and treatment
- Keywords
- Sporothrix schenckii, sporotrichosis, statins, antifungal activity, biofilm, planktonic cells, pravastatin, simvastatin, atorvastatin, 3-hydroxy-3-methylglutaryl-CoA reductase, antifungal drug interactions, amphotericin B, itraconazole, terbinafine, subcutaneous mycosis, minimum inhibitory concentration
- MeSH terms
- Antifungal Agents, Microbial Sensitivity Tests, Plankton, Sporothrix, Biofilms, Hydroxymethylglutaryl-CoA Reductase Inhibitors
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