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下调真菌病原体耳念珠菌中的必需基因。

Downregulation of Essential Genes in the Fungal Pathogen Candida auris.

机构信息

Department of Molecular Genetics, University of Toronto, Toronto, ON, Canada.

出版信息

Methods Mol Biol. 2022;2517:111-126. doi: 10.1007/978-1-0716-2417-3_9.

Abstract

The recent global emergence of the fungal pathogen Candida auris has caused significant concern given that this pathogen often exhibits resistance to multiple antifungal drug classes. In order to effectively combat C. auris infections, there is a dire need to expand our current antifungal arsenal. Essential proteins often serve as targets for antimicrobial compounds, and thus being able to study essential genes in a pathogen of interest is a critical first step in drug development. To identify and characterize essential genes in microorganisms, researchers must be able to manipulate microbial genomes using a variety of molecular biology techniques. Given the haploid genome of C. auris, genetic alterations have largely been achieved by gene deletion through homologous recombination using a drug resistance marker. However, this approach is not feasible to study essential gene function. Here, we describe a method for the study of essential genes using a tetracycline-repressible promoter replacement system, which can be used to genetically repress essential genes in C. auris and, thus, study their function. This method provides a powerful approach to assess and characterize essential gene function in an emerging fungal pathogen.

摘要

真菌病原体假丝酵母菌(Candida auris)在全球范围内的新近出现引起了极大关注,因为这种病原体通常对多种抗真菌药物类别表现出耐药性。为了有效对抗假丝酵母菌感染,我们迫切需要扩大目前的抗真菌武器库。必需蛋白通常可作为抗菌化合物的靶标,因此,能够研究感兴趣的病原体中的必需基因是药物开发的关键第一步。为了鉴定和描述微生物中的必需基因,研究人员必须能够使用各种分子生物学技术来操纵微生物基因组。鉴于假丝酵母菌的单倍体基因组,遗传改变主要通过使用耐药性标记物通过同源重组进行基因缺失来实现。然而,这种方法不适于研究必需基因的功能。在这里,我们描述了一种使用四环素可诱导的启动子替换系统来研究必需基因的方法,该方法可用于在假丝酵母菌中遗传抑制必需基因,从而研究其功能。这种方法为评估和描述新兴真菌病原体中的必需基因功能提供了一种强大的方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2740/11016342/e4e971f5dda5/nihms-1981703-f0001.jpg

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Hidden killers: human fungal infections.隐形杀手:人类真菌感染。
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