Back to Search Start Over

Mo-CBP4, a purified chitin-binding protein from Moringa oleifera seeds, is a potent antidermatophytic protein: In vitro mechanisms of action, in vivo effect against infection, and clinical application as a hydrogel for skin infection

Authors :
Pedro F.N. Souza
Ilka M. Vasconcelos
Jose T.A. Oliveira
Mirella Leite Pereira
Tiago Deiveson Pereira Lopes
Helen Paula Silva da Costa
João Xavier da Silva Neto
Paulo Carvalho de Paula
Raimunda Sâmia Nogueira Brilhante
Daniele O.B. Sousa
Source :
International Journal of Biological Macromolecules. 149:432-442
Publication Year :
2020
Publisher :
Elsevier BV, 2020.

Abstract

Dermatophytes belonging to Trichophyton ssp. are important anthropophilic and zoophilic pathogens, which developed resistance to griseofulvin, the common antifungal drug used to treat dermatophytosis. In this context, Moringa oleifera seed proteins have been described as antifungal agents with potential applications. Thus, this work aimed to evaluate the antidermatophytic in vitro, focusing on mechanisms, and in vivo potential of Mo-CBP4, purified from M. oleifera seeds. Mo-CBP4was purified after protein extraction with 50 mM Tris-HCl buffer, pH 8.0, and chromatography on chitin and CM Sepharose™ columns and antidermatophytic potential of Mo-CBP4 evaluated in vitro and in vivo. In vitro, Mo-CBP4 reduced in 50% the germination of microconidia of Trichophyton mentagrophytes at 45 μM; but did not show inhibition of mycelial growth. Mo-CBP4 (45 μM) presents the inhibitory activity even when incubated with N-acetyl- d -glucosamine (NAG). Analysis of the mechanisms of Mo-CBP4 revealed an increase in membrane permeability, ROS overproduction and damage to cell wall leading to microconidia death. Furthermore, using in vivo models, Mo-CBP4 (5, 10 and 20 mg g−1) reduced the severity and time of dermatophytosis. Altogether, these findings indicate that Mo-CBP4 has great potential for the development of novel antifungal drugs for the clinical treatment of dermatophytosis.

Details

ISSN :
01418130
Volume :
149
Database :
OpenAIRE
Journal :
International Journal of Biological Macromolecules
Accession number :
edsair.doi...........4c9fb95e8c8bc24d6a3bd651e517c7dc
Full Text :
https://doi.org/10.1016/j.ijbiomac.2020.01.257