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线粒体动力学突变体中差异调节的转录因子和ABC转运蛋白可改变……的唑敏感性

Differentially Regulated Transcription Factors and ABC Transporters in a Mitochondrial Dynamics Mutant Can Alter Azole Susceptibility of .

作者信息

Sturm Laura, Geißel Bernadette, Martin Ronny, Wagener Johannes

机构信息

Max von Pettenkofer-Institut für Hygiene und Medizinische Mikrobiologie, Medizinische Fakultät, LMU München, Munich, Germany.

Institut für Hygiene und Mikrobiologie, Julius-Maximilians-Universität Würzburg, Würzburg, Germany.

出版信息

Front Microbiol. 2020 May 26;11:1017. doi: 10.3389/fmicb.2020.01017. eCollection 2020.

Abstract

Azole resistance of the fungal pathogen is an emerging problem. To identify novel mechanisms that could mediate azole resistance in , we analyzed the transcriptome of a mitochondrial fission/fusion mutant that exhibits increased azole tolerance. Approximately 12% of the annotated genes are differentially regulated in this strain. This comprises upregulation of Cyp51A, the azole target structure, upregulation of ATP-binding cassette (ABC) superfamily and major facilitator superfamily (MFS) transporters and differential regulation of transcription factors. To study their impact on azole tolerance, conditional mutants were constructed of seven ABC transporters and 17 transcription factors. Under repressed conditions, growth rates and azole susceptibility of the mutants were similar to wild type. Under induced conditions, several transcription factor mutants showed growth phenotypes. In addition, four ABC transporter mutants and seven transcription factor mutants exhibited altered azole susceptibility. However, deletion of individual identified ABC transporters and transcription factors did not affect the increased azole tolerance of the fission/fusion mutant. Our results revealed the ability of multiple ABC transporters and transcription factors to modulate the azole susceptibility of and support a model where mitochondrial dysfunctions trigger a drug resistance network that mediates azole tolerance of this mold.

摘要

真菌病原体的唑类耐药性是一个新出现的问题。为了确定可能介导唑类耐药性的新机制,我们分析了一个表现出更高唑类耐受性的线粒体分裂/融合突变体的转录组。在该菌株中,约12%的注释基因存在差异表达。这包括唑类作用靶点结构Cyp51A的上调、ATP结合盒(ABC)超家族和主要易化子超家族(MFS)转运蛋白的上调以及转录因子的差异调节。为了研究它们对唑类耐受性的影响,构建了7个ABC转运蛋白和17个转录因子的条件突变体。在抑制条件下,突变体的生长速率和唑类敏感性与野生型相似。在诱导条件下,几个转录因子突变体表现出生长表型。此外,4个ABC转运蛋白突变体和7个转录因子突变体表现出唑类敏感性改变。然而,单个已鉴定的ABC转运蛋白和转录因子的缺失并不影响分裂/融合突变体增加的唑类耐受性。我们的结果揭示了多种ABC转运蛋白和转录因子调节唑类敏感性的能力,并支持一种模型,即线粒体功能障碍触发一个耐药网络,介导该霉菌的唑类耐受性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a4be/7264269/d5a3c569194c/fmicb-11-01017-g001.jpg

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