Antifungal activity of redox-active benzaldehydes that target cellular antioxidation

• Main Authors: Mahoney Noreen (Author), Chan Kathleen L (Author), Kim Jong H (Author), Campbell Bruce C (Author)
• Format: Book
• Published: BMC, 2011-05-01T00:00:00Z.
• Subjects: article
• Online Access: Connect to this object online.
• Notes: 10.1186/1476-0711-10-23; 1476-0711
• Keywords: Therapeutics. Pharmacology; RM1-950; Infectious and parasitic diseases; RC109-216; Microbiology; QR1-502
• Source: Annals of Clinical Microbiology and Antimicrobials, Vol 10, Iss 1, p 23 (2011)

<p>Abstract</p> <p>Background</p> <p>Disruption of cellular antioxidation systems should be an effective method for control of fungal pathogens. Such disruption can be achieved with redox-active compounds. Natural phenolic compounds can serve as potent redox cyclers that inhibit microbial growth through destabilization of cellular redox homeostasis and/or antioxidation systems. The aim of this study was to identify benzaldehydes that disrupt the fungal antioxidation system. These compounds could then function as chemosensitizing agents in concert with conventional drugs or fungicides to improve antifungal efficacy.</p> <p>Methods</p> <p>Benzaldehydes were tested as natural antifungal agents against strains of <it>Aspergillus fumigatus</it>, <it>A. flavus</it>, <it>A. terreus </it>and <it>Penicillium expansum</it>, fungi that are causative agents of human invasive aspergillosis and/or are mycotoxigenic. The yeast <it>Saccharomyces cerevisiae </it>was also used as a model system for identifying gene targets of benzaldehydes. The efficacy of screened compounds as effective chemosensitizers or as antifungal agents in formulations was tested with methods outlined by the Clinical Laboratory Standards Institute (CLSI).</p> <p>Results</p> <p>Several benzaldehydes are identified having potent antifungal activity. Structure-activity analysis reveals that antifungal activity increases by the presence of an <it>ortho</it>-hydroxyl group in the aromatic ring. Use of deletion mutants in the oxidative stress-response pathway of <it>S. cerevisiae </it>(<it>sod1</it>Δ, <it>sod2</it>Δ, <it>glr1</it>Δ) and two mitogen-activated protein kinase (MAPK) mutants of <it>A. fumigatus </it>(<it>sakA</it>Δ, <it>mpkC</it>Δ), indicates antifungal activity of the benzaldehydes is through disruption of cellular antioxidation. Certain benzaldehydes, in combination with phenylpyrroles, overcome tolerance of <it>A. fumigatus </it>MAPK mutants to this agent and/or increase sensitivity of fungal pathogens to mitochondrial respiration inhibitory agents. Synergistic chemosensitization greatly lowers minimum inhibitory (MIC) or fungicidal (MFC) concentrations. Effective inhibition of fungal growth can also be achieved using combinations of these benzaldehydes.</p> <p>Conclusions</p> <p>Natural benzaldehydes targeting cellular antioxidation components of fungi, such as superoxide dismutases, glutathione reductase, <it>etc</it>., effectively inhibit fungal growth. They possess antifungal or chemosensitizing capacity to enhance efficacy of conventional antifungal agents. Chemosensitization can reduce costs, abate resistance, and alleviate negative side effects associated with current antifungal treatments.</p>