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Sanguinarine, Isolated From Macleaya cordata , Exhibits Potent Antifungal Efficacy Against Candida albicans Through Inhibiting Ergosterol Synthesis

In recent decades, infections caused by the opportunistic fungus have increased, especially in patients with immunodeficiency. In this study, we investigated the mechanism of action of sanguinarine (SAN) against both and . SAN exhibited antifungal activity against clinical isolates, with MICs in the...

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Published in:Frontiers in microbiology 2022-06, Vol.13, p.908461-908461
Main Authors: Hu, Ziwei, Hu, Hao, Hu, Zhili, Zhong, Xiaojun, Guan, Yifu, Zhao, Yunshi, Wang, Lu, Ye, Liang, Ming, Liliang, Riaz Rajoka, Muhammad Shahid, He, Zhendan, Wang, Yan, Song, Xun
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Language:English
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Summary:In recent decades, infections caused by the opportunistic fungus have increased, especially in patients with immunodeficiency. In this study, we investigated the mechanism of action of sanguinarine (SAN) against both and . SAN exhibited antifungal activity against clinical isolates, with MICs in the range of 112.8-150.5 μM. Furthermore, scanning electron and transmission electron microscopy showed that SAN induced morphological changes as well as structure disruption in cells, including masses of cellular debris, ruptured cell walls, and membrane deformation. Flow cytometry revealed that SAN could lead to cell membrane damage, and ergosterol content analysis indicated that SAN could cause ergosterol content reduction exceeding 90%. Further, we validated the efficacy of SAN against candidiasis caused by in a murine model, and SAN significantly improved survival and reduced weight loss compared to vehicle. The treatment of 1.5 and 2.5 mg/kg/d SAN obviously reduced the fungal burden in the kidney. In addition, histopathological examination indicated that no fungal cells were observed in lung and kidney tissues after SAN treatment. Hence, this study suggests that SAN is a promising plant-derived compound for the development of an effective anticandidal agent.
ISSN:1664-302X
1664-302X
DOI:10.3389/fmicb.2022.908461