Cryptococcosis is an emerging and recalcitrant systemic infection occurring in immunocompromised patients. This invasive fungal infection is difficult to treat due to the ability of Cryptococcus neoformans and Cryptococcus laurentii to form biofilms resistant to standard antifungal treatment. The toxicity concern of these drugs has stimulated the search for natural therapeutic alternatives. Essential oil and their active components (EO-ACs) have shown to possess the variety of biological and pharmacological properties. In the present investigation the effect of six (EO-ACs) sourced from Oregano oil (Carvacrol), Cinnamon oil (Cinnamaldehyde), Lemongrass oil (Citral), Clove oil (Eugenol), Peppermint oil (Menthol) and Thyme oil (thymol) against three infectious forms; planktonic cells, biofilm formation and preformed biofilm of C. neoformans and C. laurentii were evaluated as compared to standard drugs. Data showed that antibiofilm activity of the tested EO-ACs were in the order: thymol>carvacrol>citral>eugenol=cinnamaldehyde>menthol respectively. The three most potent EO-ACs, thymol, carvacrol, and citral showed excellent antibiofilm activity at a much lower concentration against C. laurentii in comparison to C. neoformans indicating the resistant nature of the latter. Effect of the potent EO-ACs on the biofilm morphology was visualized using scanning electron microscopy (SEM) and confocal laser scanning microscopy (CLSM), which revealed the absence of extracellular polymeric matrix (EPM), reduction in cellular density and alteration in the surface morphology of biofilm cells. Further, to realize the efficacy of the EO-ACs in terms of human safety, cytotoxicity assays and co-culture model were evaluated. Thymol and carvacrol as compared to citral were the most efficient in terms of human safety in keratinocyte- Cryptococcus sp. co-culture infection model suggesting that these two can be further exploited as cost-effective and non-toxic anti-cryptococcal drugs.
The recalcitrant
biofilm formed by fungus Cryptococcus neoformans is a life-threatening pathogenic condition responsible for further
intensifying cryptococcosis. Considering the enhanced biofilm resistance
and toxicity of synthetic antifungal drugs, the search for efficient,
nontoxic, and cost-effective natural therapeutics has received a major
boost. Phenolic (thymol and carvacrol) and aldehydic (citral) terpenes
are natural and safe alternatives capable of efficient microbial biofilm
inhibition. However, the biofilm inhibition mechanism of these terpenes
still remains unclear. In this study, we adopted an integrative biophysical
and biochemical approach to elucidate the hierarchy of their action
against C. neoformans biofilm cells.
The microscopic analysis revealed disruption of the biofilm cell surface
with elevation in surface roughness and reduction in cell height.
Although all terpenes acted through ergosterol biosynthesis inhibition,
the phenolic terpenes also selectively interacted via ergosterol binding.
Further, the alterations in the fatty acid profile in response to
terpenes attenuated the cell membrane fluidity with enhanced permeability,
resulting in pore formation and efflux of the K+/intracellular
content. Additionally, mitochondrial depolarization caused higher
levels of reactive oxygen species, which led to increased lipid peroxidation
and activation of the antioxidant defense system. Indeed, the oxidative
stress caused a significant decline in the amount of extracellular
polymeric matrix and capsule sugars (mannose, xylose, and glucuronic
acid), leading to a reduced capsule size and an overall negative charge
on the cell surface. This comprehensive data revealed the mechanistic
insights into the mode of action of terpenes on biofilm inhibition,
which could be exploited for formulating novel anti-biofilm agents.
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