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烟曲霉对唑类农用杀菌剂的体外耐药性

In vitro resistance of Aspergillus fumigatus to azole farm fungicide.

作者信息

Kano Rui, Sobukawa Hideto, Murayama Somay Yamagata, Hirose Dai, Tanaka Yoko, Kosuge Yasuhiro, Hasegawa Atsuhiko, Kamata Hiroshi

机构信息

College of Bioresource Sciences, Nihon University, 1866 Kameino, Fuzisawa, Kanagawa 252-8510, Japan.

College of Bioresource Sciences, Nihon University, 1866 Kameino, Fuzisawa, Kanagawa 252-8510, Japan.

出版信息

J Infect Chemother. 2016 Mar;22(3):133-6. doi: 10.1016/j.jiac.2015.11.009. Epub 2015 Dec 19.

Abstract

Azole resistance in Aspergillus fumigatus is mainly due to a point mutation in the 14α-sterol demethylase (CYP51A) gene, which encodes the target of azole fungicides. Moreover, overexpression of CYP51B or multidrug resistance (MDR) gene is supposedly related to the mechanism of azole resistance in A. fumigatus. In this study, we tried to induce resistance to tetraconazole, an azole fungicide, in strains of A. fumigatus from a farm and then investigated mutation and expression of their CYP51A, CYP51B, and multidrug resistance (MDR) genes. Three tetraconazole resistant strains were induced and their minimum inhibitory concentration (MIC) for tetraconazole was 145 mg/L. However, the MICs of itraconazole (ITZ), posaconazole (POS), and voriconazole (VRZ) obtained by an E-test of the three tetraconazole resistant strains were 0.064-0.19 mg/L for ITZ, 0.023-0.32 mg/L for POS, and 0.047-0.064 mg/L for VRZ. No gene mutations were detected in the CYP 51A sequence amplified in these strains. RT-PCR of cyp51A and cyp51B indicated that the tetraconazole resistant strains more highly expressed these genes than the susceptible strain in tetraconazole containing medium.

摘要

烟曲霉对唑类药物的耐药性主要归因于14α-甾醇脱甲基酶(CYP51A)基因中的一个点突变,该基因编码唑类杀菌剂的作用靶点。此外,CYP51B的过表达或多药耐药(MDR)基因据推测与烟曲霉对唑类药物的耐药机制有关。在本研究中,我们试图诱导来自一个农场的烟曲霉菌株对唑类杀菌剂四氟康唑产生耐药性,然后研究其CYP51A、CYP51B和多药耐药(MDR)基因的突变和表达情况。诱导出了三株对四氟康唑耐药的菌株,它们对四氟康唑的最低抑菌浓度(MIC)为145mg/L。然而,通过对这三株对四氟康唑耐药的菌株进行E试验得到的伊曲康唑(ITZ)、泊沙康唑(POS)和伏立康唑(VRZ)的MIC分别为:ITZ为0.064 - 0.19mg/L,POS为0.023 - 0.32mg/L,VRZ为0.047 - 0.064mg/L。在这些菌株中扩增的CYP 51A序列未检测到基因突变。cyp51A和cyp51B的RT-PCR表明,在含有四氟康唑的培养基中,对四氟康唑耐药的菌株比敏感菌株更高水平地表达这些基因。

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