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编码法尼基转移酶亚基的ram1基因有助于烟曲霉的生长以及对两性霉素B的抗真菌敏感性。

ram1 gene, encoding a subunit of farnesyltransferase, contributes to growth, antifungal susceptibility to amphotericin B of Aspergillus fumigatus.

作者信息

Qiao Jianjun, Song Yan, Ling Zongxin, Liu Xia, Fang Hong

机构信息

Department of Dermatology, The First Affiliated Hospital, College of Medicine, Zhejiang University, Hangzhou, China.

Kidney Disease Center, the First Affiliated Hospital, College of Medicine, Zhejiang University, Hangzhou, China.

出版信息

Med Mycol. 2017 Nov 1;55(8):883-889. doi: 10.1093/mmy/myx002.

Abstract

Farnesylation, which is catalyzed by farnesyltransferase, is an important posttranslational process. The function of farnesyltransferase has been previously explored in Cryptococcus neoformans and Candida albicans. Aspergillus fumigatus is an important human opportunistic fungal pathogen in immunocompromised patients. Here we discover the role of the ram1 gene, encoding the β-subunit of farnesyltransferase in A. fumigatus, in the fungal growth and antifungal susceptibility. In this study the ram1 gene was disrupted using A. tumefaciens-mediated transformation. The morphology and radial growth of Δram1 were observed. Assays of disk diffusion and broth microdilution were used to determine the susceptibility of Δram1 mutant to commonly clinical used antifungals and the farnesyltransferase inhibitor manumycin A. Deletion of ram1 resulted in a reduced radial growth of A. fumigatus but did not affect the microscopic morphology. Δram1 showed increased susceptibility to the antifungal amphotericin B; however, its susceptibility to azoles and caspofungin was the same to that to the parental strain. Our data indicate that farnesyltransferase is a potential target for design new antifungal agents.

摘要

法尼基化是一种重要的翻译后修饰过程,由法尼基转移酶催化。此前已在新型隐球菌和白色念珠菌中对法尼基转移酶的功能进行了研究。烟曲霉是免疫功能低下患者重要的人类机会性真菌病原体。在此,我们发现了编码烟曲霉中法尼基转移酶β亚基的ram1基因在真菌生长和抗真菌药敏性方面的作用。在本研究中,利用根癌农杆菌介导的转化方法破坏了ram1基因。观察了Δram1的形态和径向生长情况。采用纸片扩散法和肉汤微量稀释法测定了Δram1突变体对常用临床抗真菌药物和法尼基转移酶抑制剂曼诺霉素A的药敏性。ram1基因的缺失导致烟曲霉的径向生长减少,但不影响其微观形态。Δram1对抗真菌药物两性霉素B的敏感性增加;然而,其对唑类药物和卡泊芬净的敏感性与亲本菌株相同。我们的数据表明,法尼基转移酶是设计新型抗真菌药物的潜在靶点。

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