Sweet Relief: Determining the Antimicrobial Activity of Medical Grade Honey Against Vaginal Isolates of Candida albicans
- PMID: 31505796
- PMCID: PMC6787731
- DOI: 10.3390/jof5030085
Sweet Relief: Determining the Antimicrobial Activity of Medical Grade Honey Against Vaginal Isolates of Candida albicans
Abstract
Recurrent vulvovaginal candidiasis (RVVC) is predicted to increase to almost 158 million cases annually by 2030. Extensive self-diagnosis and easily accessible over-the-counter (OTC) fungistatic drugs contribute to antifungal-resistance, illustrating the need for novel therapies. Honey possesses multiple antimicrobial mechanisms, and there is no antimicrobial resistance towards honey reported. We evaluated the susceptibility of five clinical isolates of Candida albicans and a control strain to regular honey and a medical grade honey (MGH) gel formulation (L-Mesitran, containing 40% honey and vitamins C and E) using an adapted version of the EUCAST protocol at pH 5.2, 4.6, and 4.0. 40% regular honey did not kill or inhibit C. albicans. In contrast, the minimal inhibitory concentration (MIC) of L-Mesitran was 25%-50%, while fungicidal effects occurred at a 50% concentration (MBC) of the MGH formulation, except for one strain which was not killed at pH 4.0. Overall, pH had little effect on antimicrobial activity. MGH formulation L-Mesitran has antimicrobial activity against C. albicans over a relevant pH range. The vitamin supplements or other components of L-Mesitran may enhance the antifungal activity of the honey. This study supports performing clinical trials for conditions, such as RVVC, to find an alternative to available OTC fungistatic drugs.
Keywords: antibiotic resistance; candida; candidiasis; medical grade honey; recurrent vulvovaginal candidiasis; vaginitis.
Conflict of interest statement
EvdW is a Senior Lecturer in Infectious Diseases and Epidemiology of the School of Medicine at Taylor’s University in Malaysia and declares no conflict of interest. At the time of the study, EvdW was employed by the University of Bristol, United Kingdom and is responsible for initiation of the study. JL is a Clinical Scientist specialised in Infection Sciences at Southmead Hospital, Bristol, United Kingdom and declares no conflict of interest. JL was responsible for the design of the study, susceptibility testing and presentation of the results. RH and NC are employed by Triticum Exploitatie B.V. which provided the test compounds used in this study free of charge. No other conflict of interest applies. RH and NC were responsible for drafting this manuscript but were not involved in the design or interpretation of the data.
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