4.6 Article

Hydroquinones Including Tetrachlorohydroquinone Inhibit Candida albicans Biofilm Formation by Repressing Hyphae-Related Genes

Journal

MICROBIOLOGY SPECTRUM
Volume -, Issue -, Pages -

Publisher

AMER SOC MICROBIOLOGY
DOI: 10.1128/spectrum.02536-22

Keywords

biofilm; C. albicans; hydroquinone; hyphal inhibition; tetrachlorohydroquinone

Categories

Funding

  1. Basic Science Research Program of the National Research Foundation of Korea (NRF) - Ministry of Education [2021R1I1A3A04037486]
  2. NRF - Korean government (MSIT) [2022R1C1C2006146, 2021R1A2C1008368]
  3. Priority Research Center Program of the NRF - Ministry of Education [2014R1A6A1031189]
  4. National Research Foundation of Korea [2022R1C1C2006146] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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This study found that hydroquinones, especially tetrachlorohydroquinone (TCHQ), can reduce the virulence, biofilm formation, and animal tissue adhesion of C. albicans, making them potential candidate antifungal agents against drug-resistant C. albicans strains.
Candida albicans is an opportunistic pathogenic fungus responsible for candidiasis. The pathogen readily forms antifungal agent-resistant biofilms on implanted medical devices or human tissue. Morphologic transition from yeast to filamentous cells and subsequent biofilm formation is a key virulence factor and a prerequisite for biofilm development by C. albicans. We investigated the antibiofilm and antifungal activities of 18 hydroquinones against fluconazole-resistant C. albicans. Tetrachlorohydroquinone (TCHQ) at subinhibitory concentrations (2 to 10 mu g/mL) significantly inhibited C. albicans biofilm formation with an MIC of 50 mu g/mL, whereas the backbone hydroquinone did not (MIC. 400 mu g/mL), and it markedly inhibited cell aggregation and hyphal formation. Transcriptomic analyses showed that TCHQ downregulated the expressions of several hyphae-forming and biofilm-related genes (ALS3, ECE1, HWP1, RBT5, and UME6) but upregulated hyphae- and biofilm-inhibitory genes (IFD6 and YWP1). Furthermore, it prevented C. albicans biofilm development on porcine skin and at concentrations of 20 to 50 mu g/mL was nontoxic to the nematode Caenorhabditis elegans and did not adversely affect Brassica rapa seed germination and growth. This study indicates that hydroquinones, particularly TCHQ, diminish the virulence, biofilm formation, and animal tissue adhesion of C. albicans, which suggests hydroquinones should be considered potential candidate antifungal agents against drug-resistant C. albicans strains. IMPORTANCE Persistence in chronic infections by Candida albicans is due to its ability of biofilm formation that endures conventional antifungals and host immune systems. Hence, the inhibition of biofilm formation and virulence characteristics is another mean of addressing infections. This study is a distinctive one since 18 hydroquinone analogues were screened and TCHQ efficiently inhibited the biofilm formation by C. albicans with significantly changed expressional profile of hyphae-forming and biofilm-related genes. The antibiofilm efficacy was confirmed using a porcine skin model and chemical toxicity was investigated using plant seed germination and nematode models. Our findings reveal that TCHQ can efficiently control the C. albicans biofilms and virulence characteristics.

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