In vitro evaluation of antifungal activity of monolaurin against Candida albicans biofilms

• Published in: PeerJ (San Francisco, CA) Vol. 4; p. e2148
• Main Authors: Seleem, Dalia, Chen, Emily, Benso, Bruna, Pardi, Vanessa, Murata, Ramiro M
• Format: Journal Article
• Language: English
• Published: United States PeerJ. Ltd 22.06.2016; PeerJ, Inc; PeerJ Inc
• Subjects: Analysis; Antifungal activity; Antimicrobial agent; Antimicrobial agents; Biochemistry; Biofilms; Candida; Candida albicans; Candidiasis; Care and treatment; Cell Biology; Cell culture; Coconut oil; Cytokines; Cytotoxicity; Dentistry; Drug resistance; Enzymes; Ethanol; Fibroblasts; Fluconazole; Fluorescence microscopy; Fungal infections; Gene expression; Glycerol; Health aspects; HIV; Human immunodeficiency virus; IL-1β; In vitro; Inflammation; Laboratories; Microbial drug resistance; Microbiology; Minimum inhibitory concentration; Monolaurin; Mycoses; Physical characteristics; Ribonucleic acid; RNA; Virulence factors; Candida albicans; Biofilms; Virulence factors; Proteolytic enzymes; MIC/MFC; Monolaurin; Host inflammatory response; Oral candidiasis; In vitro; Antimicrobial agent
• ISSN: 2167-8359; 2167-8359
• DOI: 10.7717/peerj.2148

Monolaurin (also known as glycerol monolaurate) is a natural compound found in coconut oil and is known for its protective biological activities as an antimicrobial agent. The nature of oral candidiasis and the increased antifungal resistance demand the search for novel antifungal therapeutic agents. In this study, we examine the antifungal activity of monolaurin against Candida albicans biofilms (strain ATCC:SC5314/MYA2876) in vitro and investigate whether monolaurin can alter gene expression of host inflammatory cytokines, IL-1α and IL-1β. In a co-culture model, oral fibroblast cells were cultured simultaneously with C. albicans for 24 hrs followed by the exposure to treatments of monolaurin (3.9-2,500 µM), positive control fluconazole (32.2 µM), and vehicle control group (1% ethanol), which was a model used to evaluate the cytotoxicity of monolaurin on fibroblasts as well as to analyze morphological characteristics of biofilms through fluorescence microscopy. In addition, the co-culture model was used for RNA extraction of oral fibroblasts to assess gene expression of host inflammatory cytokines, using quantitative real-time PCR. Our results showed the MIC and MFC of monolaurin were in the range 62.5-125 µM and 125-250 µM, respectively. Biofilm antifungal assay showed significant reduction in Log (CFU/ml) of biofilms treated with 1,250 and 2,500 µM of 1-monolaurin when compared to the control groups . There was also a significant down-regulation of IL-1α and IL-1β in the co-culture treated with monolaurin. It can be concluded that monolaurin has a potential antifungal activity against C. albicans and can modulate the pro-inflammatory response of the host.