In vitro evaluation of antimicrobial activity of 1-lauroyl-rac-glycerol on Candidaalbicans biofilms

Herman Ostrow School of Dentistry, University of Southern California, Los Angeles, California, United States
Department of Periodontology Diagnostic Sciences, Dental Hygiene and Biomedical Science, University of Southern California, Los Angeles, CA, United States
Department of Physiological Sciences, Piracicaba Dental School, State University of Campinas, Piracicaba, SP, Brazil
Herman Ostrow School of Dentistry, University of Southern California, Los Angeles, Ca, USA
DOI
10.7287/peerj.preprints.1717v1
Subject Areas
Cell Biology, Microbiology, Dentistry
Keywords
Candida albicans, in vitro, antimicrobial agent, monolaurin, biofilms., virulence factors, proteolytic enzymes, oral candidiasis, MIC/MFC, host inflammatory response
Copyright
© 2016 Chen et al.
Licence
This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ PrePrints) and either DOI or URL of the article must be cited.
Cite this article
Chen E, Seleem D, Benso B, Pardi V, Murata RM. 2016. In vitro evaluation of antimicrobial activity of 1-lauroyl-rac-glycerol on Candidaalbicans biofilms . PeerJ PrePrints 4:e1717v1

Abstract

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, culminate the need for investigating 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 how monolaurin may alter specific host inflammatory markers, such as gene expression of inflammatory cytokines IL-1α and IL-1β, as illustrated in co-culture models. The results from three groups were compared: 1- monolaurin (in the range of 3.9-2500 μM), positive control fluconazole (322 μM), and vehicle control group 1% Ethanol (v/v) The MIC and MFC of monolaurin were in the range 62.5-125 µM and 125-250 µM, respectively. The results show significant reduction in Log (CFU/ ml) of biofilms treated with 1250 and 2500 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 biofilms treated with monolaurin. It can be concluded that monolaurin has a potential antifungal activity against C. albicans and can modulate the host’s pro-inflammatory response.

Author Comment

This is a submission to PeerJ for review.

Supplemental Information

Biofilms fungal load results with monolaurin treatments

DOI: 10.7287/peerj.preprints.1717v1/supp-1

Real-time PCR Quantitative analysis of virulence factors of C. albicans and fibroblasts inflammatory cytokines gene expression after treatment with monolaurin

DOI: 10.7287/peerj.preprints.1717v1/supp-2

Toxicity of monolaurin on fibroblasts

DOI: 10.7287/peerj.preprints.1717v1/supp-3

Minimum inhibitory concentration (MIC) of monolaurin on c. albicans

DOI: 10.7287/peerj.preprints.1717v1/supp-4

Proteolytic enzyme analysis of C. albicans proteinase and phospholipase after biofilms treatments with monolaurin

DOI: 10.7287/peerj.preprints.1717v1/supp-5