Terpenoids with antifungal activity trigger mitochondrial dysfunction in Saccharomyces cerevisiae
- Autores: Haque E.1, Irfan S.1, Kamil M.1, Sheikh S.1, Hasan A.2, Ahmad A.2, Lakshmi V.3, Nazir A.4, Mir S.S.2
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Afiliações:
- Department of Biosciences, Faculty of Applied Sciences
- Department of Bioengineering, Faculty of Engineering
- Department of Biochemistry
- Laboratory of Functional Genomics and Molecular Toxicology, Division of Toxicology
- Edição: Volume 85, Nº 4 (2016)
- Páginas: 436-443
- Seção: Experimental Articles
- URL: https://bakhtiniada.ru/0026-2617/article/view/162702
- DOI: https://doi.org/10.1134/S0026261716040093
- ID: 162702
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Resumo
A number of pathogenic fungi like Candida, cannot survive upon damage to mitochondrial DNA (mtDNA) while the budding yeast can tolerate the damage therefore we chose Saccharomyces cerevisiae as a model system for this study. Since a number of potent antifungals have originated from various natural sources, we decided to use a triterpenoid and tetraterpenoid in this study as an antifungal agent. Our data clearly indicates that terpenoids play a role in diminishing the mitochondrial content which results in altered level of reactive oxygen species (ROS) and ATP generation. Here, we report that triterpenoid and tetraterpenoid display MIC at 100 and 120 μg /mL respectively against S. cerevisiae. At MIC dose triterpenoid (Lupeol) treated cells showed relatively higher mitochondrial dysfunction as compared to tetraterpenoid, resulting high level of ROS generation in triterpenoid in comparison to tetraterpenoid treated cells. Whereas the ATP level decreases in triterpenoid treated cells while it remains same in tetraterpenoid treated cells. Hence triterpenoid showed more potent antifungal activity as compared to the tetraterpenoid at their MIC by targeting mitochondrial integrity. The outcome of the study is to decipher the mode of action of terpenoids which will be useful in designing of improved antifungal therapies and also accelerate the development of translational applications.
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Sobre autores
E. Haque
Department of Biosciences, Faculty of Applied Sciences
Email: snobermir@gmail.com
Índia, Lucknow, 226026
S. Irfan
Department of Biosciences, Faculty of Applied Sciences
Email: snobermir@gmail.com
Índia, Lucknow, 226026
M. Kamil
Department of Biosciences, Faculty of Applied Sciences
Email: snobermir@gmail.com
Índia, Lucknow, 226026
S. Sheikh
Department of Biosciences, Faculty of Applied Sciences
Email: snobermir@gmail.com
Índia, Lucknow, 226026
A. Hasan
Department of Bioengineering, Faculty of Engineering
Email: snobermir@gmail.com
Índia, Lucknow, 226026
A. Ahmad
Department of Bioengineering, Faculty of Engineering
Email: snobermir@gmail.com
Índia, Lucknow, 226026
V. Lakshmi
Department of Biochemistry
Email: snobermir@gmail.com
Índia, Lucknow, 226003
A. Nazir
Laboratory of Functional Genomics and Molecular Toxicology, Division of Toxicology
Email: snobermir@gmail.com
Índia, Lucknow, 226001
S. Mir
Department of Bioengineering, Faculty of Engineering
Autor responsável pela correspondência
Email: snobermir@gmail.com
Índia, Lucknow, 226026
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