Pereira Fillipe de Oliveira, Mendes Juliana Moura, Lima Igara Oliveira, Mota Kelly Samara de Lira, Oliveira Wylly Araújo de, Lima Edeltrudes de Oliveira
Unidade Acadêmica de Saúde, Centro de Educação e Saúde, Universidade Federal de Campina Grande , Cuité , Brasil and.
Pharm Biol. 2015 Feb;53(2):228-34. doi: 10.3109/13880209.2014.913299. Epub 2014 Nov 21.
Trichophyton rubrum is the most common fungus causing chronic dermatophytosis in humans. Antifungal activity of promising agents is of great interest. Geraniol and citronellol are monoterpenes with antimicrobial properties.
This study aimed to investigate the inhibitory effects and possible mechanism of antifungal activity of geraniol and citronellol against strains of T. rubrum.
The minimum inhibitory concentration (MIC) of each drug against 14 strains was determined by broth microdilution. The effects of the drugs on dry mycelial weight, conidial germination, infectivity on human nail fragments, and morphogenesis of T. rubrum were analyzed. The effects on the cell wall (test with sorbitol) and cell membrane (release of intracellular material and ergosterol biosynthesis) were investigated.
MIC values of geraniol ranged between 16 and 256 µg/mL while citronellol showed MIC values from 8 to 1024 µg/mL. The drugs (MIC and 2 × MIC) inhibited the mycelial growth, conidia germination, and fungal growth on nail fragments. The drugs (half of MIC) induced the formation of wide, short, and crooked hyphae in T. rubrum morphology. With sorbitol, geraniol MIC was increased by 64-fold and citronellol by 32-fold. The drugs caused leakage of intracellular material and inhibited ergosterol biosynthesis.
The results suggest that the drugs damage cell wall and cell membrane of T. rubrum through a mechanism that seems to involve the inhibition of the ergosterol biosynthesis.
This study confirms that geraniol and citronellol can be regarded as potential drugs for controlling T. rubrum growth, with great potential against agents of dermatophytosis.
红色毛癣菌是引起人类慢性皮肤癣菌病最常见的真菌。有前景的抗真菌药物的活性备受关注。香叶醇和香茅醇是具有抗菌特性的单萜类化合物。
本研究旨在探讨香叶醇和香茅醇对红色毛癣菌菌株的抑制作用及其抗真菌活性的可能机制。
采用肉汤微量稀释法测定每种药物对14株菌株的最低抑菌浓度(MIC)。分析药物对红色毛癣菌干菌丝重量、分生孢子萌发、对人指甲碎片的感染性及形态发生的影响。研究药物对细胞壁(用山梨醇试验)和细胞膜(细胞内物质释放及麦角甾醇生物合成)的影响。
香叶醇的MIC值在16至256μg/mL之间,而香茅醇的MIC值为8至1024μg/mL。这些药物(MIC和2×MIC)抑制了菌丝生长、分生孢子萌发以及在指甲碎片上的真菌生长。这些药物(MIC的一半)诱导红色毛癣菌形态形成宽、短且弯曲的菌丝。使用山梨醇时,香叶醇的MIC增加64倍,香茅醇增加32倍。这些药物导致细胞内物质泄漏并抑制麦角甾醇生物合成。
结果表明,这些药物通过一种似乎涉及抑制麦角甾醇生物合成的机制破坏红色毛癣菌的细胞壁和细胞膜。
本研究证实香叶醇和香茅醇可被视为控制红色毛癣菌生长的潜在药物,对皮肤癣菌病病原体具有巨大潜力。