da Silva Neto Benedito Rodrigues, Carvalho Patrícia Fernanda Zambuzzi, Bailão Alexandre Melo, Martins Wellington Santos, Soares Célia Maria de Almeida, Pereira Maristela
Departamento de Bioquímica e Biologia Molecular, Laboratório de Biologia Molecular, Instituto de Ciências Biológicas, ICBII, Campus II, Universidade Federal de Goiás, C,P, 131, 74001-970 Goiânia, GO, Brazil.
BMC Genomics. 2014 Apr 1;15:254. doi: 10.1186/1471-2164-15-254.
Itraconazole is currently used to treat paracoccidioidomycosis. The mechanism of action of azoles has been elucidated in some fungi, although little is known regarding its mechanism of action in Paracoccidioides spp. The present work focused on identification of regulated transcripts using representational difference analysis of Paracoccidioides spp. yeast cells treated with itraconazole for 1 and 2 h.
Paracoccidioides Pb01 genes up-regulated by itraconazole included genes involved in cellular transport, metabolism/energy, transcription, cell rescue, defense and virulence. ERG11, ERG6, ERG3, ERG5 and ERG25 were up-regulated at multiple time points. In vivo infection experiments in mice corroborated the in vitro results. Ergosterol levels and distribution were evaluated in Paracoccidioides Pb18 yeast cells, and the results demonstrate that both factors were changed in the fungus treated with itraconazole.
To our knowledge, this is the first transcriptional analysis of Paracoccidioides spp. exposed to a triazole drug. Here acetyl seems to be intensively produced from different metabolic pathways to produce ergosterol by the action of ergosterol synthesis related enzymes, which were also affected in other fungi. Among the genes affected, we identified genes in common with other fungi, as well as genes unique to Paracoccidioides Pb01. Those genes could be considered target to new drugs. Voltage-gated Ca2+ alpha subunit (CAV), Tetracycline resistance protein (TETA) and Hemolisyn-iii channel protein (HLYiii) were found only here and a probably involvement with resistance to itraconazole could be investigated in the future. However our findings do not permit inference to current clinical practice.
伊曲康唑目前用于治疗副球孢子菌病。尽管关于其在副球孢子菌属中的作用机制知之甚少,但唑类药物的作用机制已在一些真菌中得到阐明。本研究聚焦于使用代表性差异分析来鉴定经伊曲康唑处理1小时和2小时的副球孢子菌属酵母细胞中受调控的转录本。
伊曲康唑上调的副球孢子菌Pb01基因包括参与细胞转运、代谢/能量、转录、细胞拯救、防御和毒力的基因。ERG11、ERG6、ERG3、ERG5和ERG25在多个时间点均上调。小鼠体内感染实验证实了体外实验结果。对副球孢子菌Pb18酵母细胞中的麦角固醇水平和分布进行了评估,结果表明在用伊曲康唑处理的真菌中这两个因素均发生了变化。
据我们所知,这是首次对暴露于三唑类药物的副球孢子菌属进行转录分析。在这里,似乎通过不同代谢途径大量产生乙酰基,以通过麦角固醇合成相关酶的作用来产生麦角固醇,这些酶在其他真菌中也受到影响。在受影响的基因中,我们鉴定出了与其他真菌共有的基因以及副球孢子菌Pb01特有的基因。这些基因可被视为新药的靶点。仅在此处发现了电压门控Ca2+α亚基(CAV)、四环素抗性蛋白(TETA)和溶血素-iii通道蛋白(HLYiii),未来可研究它们可能与对伊曲康唑的抗性有关。然而,我们的研究结果不允许推断当前的临床实践。