In Vitro activity of Manuka Honey and polyhexamethylene biguanide on filamentous fungi and toxicity to human cell lines

• Published in: Medical mycology (Oxford) 2017-04, Vol.55 (3), p.334-343
• Main Authors: Yabes, Joseph M., White, Brian K., Murray, Clinton K., Sanchez, Carlos J., Mende, Katrin, Beckius, Miriam L., Zera, Wendy C., Wenke, Joseph C., Akers, Kevin S.
• Format: Article
• Language: English
• Subjects: Biguanides - pharmacology; Biguanides - toxicity; Cell Line; Cell Survival - drug effects; Disinfectants - pharmacology; Disinfectants - toxicity; Fibroblasts - drug effects; Fibroblasts - physiology; Fungi - drug effects; Fungi - physiology; Honey; Humans; Keratinocytes - drug effects; Keratinocytes - physiology; Lethal Dose 50; Microbial Sensitivity Tests; Original; Osteoblasts - drug effects; Osteoblasts - physiology; Time Factors
• ISSN: 1369-3786; 1460-2709
• DOI: 10.1093/mmy/myw070

Abstract Soft-tissue invasive fungal infections are increasingly recognized as significant entities directly contributing to morbidity and mortality. They complicate clinical care, requiring aggressive surgical debridement and systemic antifungal therapy. To evaluate new topical approaches to therapy, we examined the antifungal activity and cytotoxicity of Manuka Honey (MH) and polyhexamethylene biguanide (PHMB). The activities of multiple concentrations of MH (40%, 60%, 80%) and PHMB (0.01%, 0.04%, 0.1%) against 13 clinical mould isolates were evaluated using a time-kill assay between 5 min and 24 h. Concentrations were selected to represent current clinical use. Cell viability was examined in parallel for human epidermal keratinocytes, dermal fibroblasts and osteoblasts, allowing determination of the 50% viability (LD50) concentration. Antifungal activity of both agents correlated more closely with exposure time than concentration. Exophiala and Fusarium growth was completely suppressed at 5 min for all PHMB concentrations, and at 12 and 6 h, respectively, for all MH concentrations. Only Lichtheimia had persistent growth to both agents at 24 h. Viability assays displayed concentration-and time-dependent toxicity for PHMB. For MH, exposure time predicted cytotoxicity only when all cell types were analyzed in aggregate. This study demonstrates that MH and PHMB possess primarily time-dependent antifungal activity, but also exert in vitro toxicity on human cells which may limit clinical use. Further research is needed to determine ideal treatment strategies to optimize antifungal activity against moulds while limiting cytotoxicity against host tissues in vivo.