Thidiazuron, a phenyl-urea cytokinin, inhibits ergosterol synthesis and attenuates biofilm formation of Candida albicans.

Pandurangan Harikrishnan, Balamani Arayambath, Vijay Karthik Jayaraman, Kanimozhi Ekambaram, Emad A Ahmed, Palanisamy Senthilkumar, Hairul-Islam Mohamed Ibrahim, Arjunan Sundaresan, Krishnaraj Thirugnanasambantham

Journal: World journal of microbiology & biotechnology 2022;38(12):224

PMID: 36114903

Abstract

Candida albicans is a common human fungal pathogen that colonizes mucosa and develops biofilm in the oral cavity that causes oral candidiasis. It has been reported that cytochrome P450 enzyme (CYP51), a vital part of the ergosterol synthesis cascade, is associated with Candida infections and its biofilm formation. Thidiazuron, a phenyl-urea cytokinin, exhibits anti-senescence and elicitor activity against fungal infection in plants. However, how Thidiazuron impacts C. albicans biofilm formation is still uncertain. Here, we aimed to investigate the effects of a Thidiazuron against the growth and biofilm formation properties of C. albicans using in silico and in vitro experimental approaches. A preliminary molecular docking study revealed potential interaction between Thidiazuron and amino acid residues of CYP51. Further in vitro antifungal susceptibility test, scanning electron microscopy (SEM) and time kill analysis revealed the anti-fungal activity of Thidiazuron in both dose and time-dependent manner. Crystal violet staining, 2,3-bis-(2-methoxy-4-nitro-5-sulfophenyl)-2H-tetrazolium-5-carboxanilide (XTT) reduction assay revealed 50% inhibition in C. albicans biofilm by Thidiazuron at concentrations 11 and 19 µM respectively. Acridine orange staining assay visually confirmed the biofilm inhibitory potential of Thidiazuron. The gene expression study showed that Thidiazuron treatment down regulated the expression of genes involved in ergosterol synthesis (ERG3, ERG11, ERG25), cell adhesion (ASL3, EAP1), and hyphae development (EFG1, HWP1, SAP5) in C. albicans. Wherease, the expression of negative transcription regulator of hyphae (NRG1) was upregulated (5.7-fold) by Thidiazuron treatment. Collectively, our data suggest that Thidiazuron is a robust antifungal compound and an outstanding biofilm inhibitor, which may promise further therapeutic development due to CYP51 binding and inhibition of ergosterol formation against C. albicans.

© 2022. The Author(s), under exclusive licence to Springer Nature B.V.

Address: Pondicherry Centre for Biological Science and Educational Trust, Sundararaja Nagar, Pondicherry, 605004, India.; Teeth "N" Jaws Center, Lake Area, Chennai, 600034, Tamil Nadu, India.; Dept.of Orthodontics, Faculty of Dental Sciences, SGT University, Gurugram, 122505, Haryana, India.; Department of Orthodontics, Mahatma Gandhi Postgraduate Institute of Dental Sciences, Pondicherry, 605006, India.; Dencity Dental Clinic, Chennai, 600073, Tamil Nadu, India.; Endodontic Clinic, Tamil Nadu, Mettur Dam, Salem, 636404, Tamil Nadu, India.; Biological Science College of Science, King Faisal University, Al Ahsa, 31982, Saudi Arabia.; Department of Genetic Engineering, SRM Institute of Science and Technology, Kattankulathur, 603203, Tamil Nadu, India.; Pondicherry Centre for Biological Science and Educational Trust, Sundararaja Nagar, Pondicherry, 605004, India.; Biological Science College of Science, King Faisal University, Al Ahsa, 31982, Saudi Arabia.; Pondicherry Centre for Biological Science and Educational Trust, Sundararaja Nagar, Pondicherry, 605004, India.; Pondicherry Centre for Biological Science and Educational Trust, Sundararaja Nagar, Pondicherry, 605004, India. [email protected].; Department of Biotechnology, Saveetha School of Engineering, Saveetha Institute of Medical and Technical Sciences, Chennai, India. [email protected].

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