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法氏马杜拉放线菌对伊曲康唑的耐药性与编码细胞色素P450 14-α甾醇去甲基酶(CYP51)基因的一个独特同源物有关。

Itraconazole resistance in Madurella fahalii linked to a distinct homolog of the gene encoding cytochrome P450 14-α sterol demethylase (CYP51).

作者信息

Yoshioka Isato, Fahal Ahmed Hassan, Kaneko Satoshi, Cao Wei, Yaguchi Takashi

机构信息

Medical Mycology Research Center, Chiba University, Chiba, Chiba, Japan.

Research Institute for Science and Engineering, Waseda University, Shinjuku-ku, Tokyo, Japan.

出版信息

PLoS Negl Trop Dis. 2025 Mar 27;19(3):e0012623. doi: 10.1371/journal.pntd.0012623. eCollection 2025 Mar.

Abstract

BACKGROUND

Mycetoma is a deep fungal infection caused by several microorganisms, with Madurella mycetomatis being the most common causative agent. Another related species, Madurella fahalii, is also known to cause eumycetoma. However, unlike M. mycetomatis, M. fahalii exhibits resistance to itraconazole, the standard treatment for eumycetoma, and the underlying cause of this resistance remains unknown. Therefore, understanding the mechanism of this resistance is critical for developing more effective therapies.

PRINCIPAL FINDINGS

Using the high-quality draft genome sequence of Madurella fahalii IFM 68171, we identified two copies of the gene encoding cytochrome P450 14-α sterol demethylase (CYP51), the target enzyme of itraconazole. These include a gene conserved among Madurella species (Mfcyp51A1) and a M. fahalii-specific gene (Mfcyp51A2). Both genes are actively transcribed in M. fahalii and are upregulated in response to itraconazole. Furthermore, heterologous expression in Saccharomyces cerevisiae revealed that transformants carrying the Mfcyp51A2 gene exhibited reduced susceptibility to itraconazole compared to those with Mfcyp51A1.

CONCLUSION

We demonstrated that itraconazole resistance in M. fahalii may be attributed to the presence of an additional CYP51 gene. This study represents the first report on the physiological characteristics of Madurella species using genetic engineering techniques.

摘要

背景

足菌肿是由多种微生物引起的深部真菌感染,其中马杜拉足菌肿霉是最常见的病原体。另一种相关物种法哈勒马杜拉菌也已知会引起真菌性足菌肿。然而,与马杜拉足菌肿霉不同,法哈勒马杜拉菌对真菌性足菌肿的标准治疗药物伊曲康唑表现出耐药性,而这种耐药性的根本原因仍然未知。因此,了解这种耐药机制对于开发更有效的治疗方法至关重要。

主要发现

利用法哈勒马杜拉菌IFM 68171的高质量基因组草图序列,我们鉴定出编码细胞色素P450 14-α甾醇去甲基酶(CYP51)的基因有两个拷贝,CYP51是伊曲康唑的靶酶。其中包括一个在马杜拉菌属物种中保守的基因(Mfcyp51A1)和一个法哈勒马杜拉菌特异性基因(Mfcyp51A2)。这两个基因在法哈勒马杜拉菌中均活跃转录,并在伊曲康唑作用下上调。此外,在酿酒酵母中的异源表达表明,携带Mfcyp51A2基因的转化体与携带Mfcyp51A1基因的转化体相比,对伊曲康唑表现出更低的敏感性。

结论

我们证明法哈勒马杜拉菌对伊曲康唑的耐药性可能归因于额外存在的一个CYP51基因。本研究是利用基因工程技术对马杜拉菌属物种生理特性的首次报道。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7fe7/11964275/bff55184fd7d/pntd.0012623.g001.jpg

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