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

被引:18
|
作者
Pereira Lopes, Tiago Deiveson [1 ]
Noronha Souza, Pedro Filho [1 ]
Silva da Costa, Helen Paula [1 ]
Pereira, Mirella Leite [1 ]
da Silva Neto, Joao Xavier [1 ]
de Paula, Paulo Carvalho [1 ]
Nogueira Brilhante, Raimunda Samia [2 ]
Abreu Oliveira, Jose Tadeu [1 ]
Vasconcelos, Ilka Maria [1 ]
Bezerra Sousa, Daniele Oliveira [1 ]
机构
[1] Univ Fed Ceara, Dept Biochem & Mol Biol, Fortaleza, Ceara, Brazil
[2] Univ Fed Ceara, Dept Pathol, Fortaleza, Ceara, Brazil
关键词
Moringa oleifera; Chitin-binding protein; Anti-dermatophytic potential; ANTIFUNGAL ACTIVITY; ESSENTIAL OIL; TRICHOPHYTON-MENTAGROPHYTES; THIOCARBAMATE; RESISTANCE; EXTRACTS; INSIGHTS; ALBUMIN; ANTIGEN; PLANTS;
D O I
10.1016/j.ijbiomac.2020.01.257
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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 MoCBP4, purified from M. oleifera seeds. Mo-CBP4 was purified after protein extraction with 50 mM Tris-HCl buffer, pH 8.0, and chromatography on chitin and CM Sepharose (TM) columns and antidermatophytic potential of MoCBP4 evaluated in vitro and in vivo. In vitro, Mo-CBP4 reduced in 50% the germination of microconidia of Trichophyton mentagrophytes at 45 mu M; but did not show inhibition of mycelial growth. Mo-CBP4 (45 mu M) presents the inhibitory activity even when incubated with N-acetyl-n-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 anti fungal drugs for the clinical treatment of dermatophytosis. (C) 2020 Elsevier B.V. All rights reserved.
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页码:432 / 442
页数:11
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