Antifungal and Antibiofilm Activity of Riparin III against Dermatophytes

Author:

Silva Emanuel Pereira1,Rocha Marcelo Antônio Nóbrega da1,Silva Risley Nikael Medeiros1,Moura-Mendes Juliana2ORCID,Sousa Gabriela Ribeiro de3,de Souza-Ferrari Jailton4ORCID,Barbosa-Filho José Maria3ORCID,Lima Edeltrudes de Oliveira5,Pereira Fillipe de Oliveira1

Affiliation:

1. Fungi Research Group, Biochemistry Laboratory, Academic Unit of Health, Education and Health Center, Federal University of Campina Grande, Cuité 58175-000, PB, Brazil

2. Centro Multidisciplinario de Investigaciones Tecnológicas, Universidad Nacional de Asunción, San Lorenzo 111421, Paraguay

3. Postgraduate Program in Natural and Synthetic Bioactive Products, Pharmaceutical Sciences Department, Federal University of Paraiba, João Pessoa 58051-900, PB, Brazil

4. Department of Chemistry, Federal University of Paraiba, João Pessoa 58051-900, PB, Brazil

5. Department of Pharmaceutical Sciences, Federal University of Paraiba, João Pessoa 58051-900, PB, Brazil

Abstract

The ability of dermatophytes to develop biofilms is possibly involved in therapeutic failure because biofilms impair drug effectiveness in the infected tissues. Research to find new drugs with antibiofilm activity against dermatophytes is crucial. In this way, riparins, a class of alkaloids that contain an amide group, are promising antifungal compounds. In this study, we evaluated the antifungal and antibiofilm activity of riparin III (RIP3) against Trichophyton rubrum, Microsporum canis, and Nannizzia gypsea strains. We used ciclopirox (CPX) as a positive control. The effects of RIP3 on fungal growth were evaluated by the microdilution technique. The quantification of the biofilm biomass in vitro was assessed by crystal violet, and the biofilm viability was assessed by quantifying the CFU number. The ex vivo model was performed on human nail fragments, which were evaluated by visualization under light microscopy and by quantifying the CFU number (viability). Finally, we evaluated whether RIP3 inhibits sulfite production in T. rubrum. RIP3 inhibited the growth of T. rubrum and M. canis from 128 mg/L and N. gypsea from 256 mg/L. The results showed that RIP3 is a fungicide. Regarding antibiofilm activity, RIP3 inhibited biofilm formation and viability in vitro and ex vivo. Moreover, RIP3 inhibited the secretion of sulfite significantly and was more potent than CPX. In conclusion, the results indicate that RIP3 is a promising antifungal agent against biofilms of dermatophytes and might inhibit sulfite secretion, one relevant virulence factor.

Publisher

MDPI AG

Subject

Plant Science,Ecology, Evolution, Behavior and Systematics,Microbiology (medical)

Reference43 articles.

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3. The Prevalence of Dermatophytoses in Brazil: A Systematic Review;Gomes;J. Med. Microbiol.,2021

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5. Springer, C. (2017). Immunogenetics of Fungal Diseases, Springer International Publishing.

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