Title

Solasodine inhibits Candida albicans adhesion at sub-MIC level

Document Type

Conference Proceeding

Publication Date

2016

Abstract

Objectives: To investigate the in vitro effects of solasodine on the adhesion of Candida albicans to buccal epithelial cells.

Methods: Buccal epithelial cells (BECs) were collected from healthy adults by gently rubbing the cheek mucosa with sterile swabs, and washed twice in phosphate-buffered saline. Equal volumes of BECs (105 cells/mL) and wild type C. albicans SC5314 (107 cells/mL) were incubated at 37oC for 1 h with gentle agitation in the absence or presence of sub-MIC level (60 μM) of solasodine, and filtered through 12 μm pore polycarbonate filters. Unattached cells were washed away, and the BECs were air-dried and Gram’s stained. Attached fungal cells were counted under light microscope in 50 BECs. qRT-PCR was used to evaluate variations in expression of adhesion-related genes in solasodine-treated fungal cells. Total RNA was extracted using SV Total RNA Isolation System and reverse transcribed with Superscript II. Gene expression was determined by Fast SYBR Green Master Mix with gene-specific primers, and reactions were run: 95oC incubation for 20 s, followed by 40 cycles of 95oC incubation for 1 s and 60oC for 20 s. EFB1 was used for reference. All experiments were performed in triplicate in three different occasions. Student’s t test was used, and a P-value of

Results: Solasodine inhibited C. albicans adhesion to BECs by ~52% (P < 0.05). qRT-PCR analysis showed that while the gene expression of BCR1 was not affected, the gene expression of ALS3, ECE1, and HWP1 was reduced. However, expression of ALS1 was promoted.

Conclusions: The collective data of the present study suggest that solasodine suppresses C. albicans adhesion to the BECs via downregulation of the expression of adhesion-related genes ALS3, ECE1, and HWP1. This provides insights for further investigation of this compound with respect to its antifungal effectiveness in clinical intervention studies.

Source Publication

The 94th General Session & Exhibition of the International Association of Dental Research, Seoul, Republic of Korea

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