铜绿假单胞菌arna甲基转移酶在抗生素耐药性中的作用

Pablo Valderrama-Carmona, Jaison H. Cuartas, Diana Castaño, M. Corredor
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引用次数: 3

摘要

甲基转移酶在革兰氏阴性菌的氨基糖苷耐药中起着重要作用,近年来对其机制进行了一些研究,特别是在大肠杆菌中;然而,对于其他耐药细菌,如铜绿假单胞菌,仍未得到解决。尽管在确定耐药性获取方面存在障碍,但高通量方法(基因组学、转录组学和蛋白质组学)已经允许以系统的方式进行数据挖掘和分析。同样,同源基因或蛋白质的生物信息学模型已经允许阐明这种病原体中出现的耐药性。铜绿假单胞菌是一种细菌耐药治疗,因为几乎所有已知的耐药机制都可以使用该模型来描述,特别是RNA甲基转移酶。RNA甲基转移酶对核糖体RNA进行甲基化或去甲基化,以允许或限制抗生素耐药性的发展。在铜绿假单胞菌中发现Kgm和Kam甲基转移酶家族,并赋予对几种氨基糖苷的抗性。原生甲基化的缺失也可能导致抗性表型。铜绿假单胞菌RsmG与水热菌蛋白具有高度的结构同源性。今天,分子数据将促进抗生素治疗铜绿假单胞菌的新范式。本章概述了铜绿假单胞菌的甲基转移酶在核糖体甲基化或去甲基化诱导的抗生素耐药性中所起的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Role ofPseudomonas aeruginosaRNA Methyltransferases in Antibiotic Resistance
Methyltransferases play a fundamental role in aminoglycoside resistance of Gram-negative bacteria, and some of its mechanisms were described in the past years, especially in Escherichia coli ; however, it remains unsolved for other resistant bacteria such as Pseudomonas aeruginosa . Despite hurdles to determine resistance acquisition, high-throughput approaches (genomics, transcriptomics, and proteomics) have allowed data mining and analysis in a systemic way. Likewise, bioinformatics modelling of homologous genes or proteins has permitted to eluci-date the emerging resistance in this pathogen. P. aeruginosa is a bacterial resistance treat since practically all known resistance mechanisms can be described using this model, particularly RNA methyltransferases. The RNA methyltransferases perform methylation or demethylation of ribosomal RNA to allow or restrict the antibiotic resistance development. The Kgm and Kam methyltransferases families are found in P. aeruginosa and confer resistance to several aminoglycosides. Loss of native methylations may also confer a resistant phenotype. The P. aeruginosa RsmG has high structural homology with Thermus aquaticus protein. Today, molecular data will promote a new paradigm on antibiotic therapy for treatment against P. aeruginosa . This chapter provides an overview of what role P. aeruginosa’ s methyltransferases play in antibiotic resistance, induced by methylation or demethylation in the ribosome.
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