Gruhn C M, Boyle S M
Department of Biology, College of Arts and Sciences, Virginia-Maryland Regional College of Veterinary Medicine, Virginia Polytechnic Institute and State University, Blacksburg 24061.
J Med Vet Mycol. 1991;29(2):63-72.
The minimum inhibitory concentrations (MICs) of three known irreversible inhibitors of polyamine synthesis, alpha-difluoromethylornithine (DFMO) and monofluoromethyldehydroornithine methylester (MFMOme), inhibitors of ornithine decarboxylase (ODC) and alpha-difluoromethylarginine (DFMA), an inhibitor of arginine decarboxylase (ADC), were determined for 10 species of dermatophytic fungi. Trichophyton species were generally more sensitive to these inhibitors than Microsporum species. Both genera produced arginase, and treatment of members of either genus with DFMO or DFMA resulted in an inhibition of ODC activity and a depletion of cellular polyamines. However, conversion of labelled DFMA to DFMO, either in vivo or in vitro, could not be demonstrated in spite of both genera producing arginase. The ultrastructure of cells cultured in the presence of either DFMO or DFMA was similar, and revealed disruption of calcium metabolism, an increase in mitochondrial number and alterations to membrane systems. DFMA and DFMO also inhibited sporulation in Microsporum gypseum. Our findings indicate that DFMO limits the growth of dermatophytes by direct inhibition of ODC and lowering of cellular polyamine levels; in contrast, DFMA inhibits polyamine synthesis in an unspecified manner as ADC activity was undetected.
测定了三种已知的多胺合成不可逆抑制剂,即鸟氨酸脱羧酶(ODC)抑制剂α-二氟甲基鸟氨酸(DFMO)和单氟甲基脱氢鸟氨酸甲酯(MFMOme),以及精氨酸脱羧酶(ADC)抑制剂α-二氟甲基精氨酸(DFMA)对10种皮肤癣菌的最低抑菌浓度(MIC)。毛癣菌属通常比小孢子菌属对这些抑制剂更敏感。两个属都产生精氨酸酶,用DFMO或DFMA处理这两个属的成员都会导致ODC活性受到抑制和细胞内多胺耗尽。然而,尽管两个属都产生精氨酸酶,但在体内或体外均未证实标记的DFMA能转化为DFMO。在DFMO或DFMA存在下培养的细胞超微结构相似,显示钙代谢紊乱、线粒体数量增加以及膜系统改变。DFMA和DFMO还抑制了石膏样小孢子菌的孢子形成。我们的研究结果表明,DFMO通过直接抑制ODC和降低细胞内多胺水平来限制皮肤癣菌的生长;相比之下,由于未检测到ADC活性,DFMA以一种未明确的方式抑制多胺合成。