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肠道细菌的多抗生素耐药操纵子控制 DNA 修复和外膜完整性。

The multiple antibiotic resistance operon of enteric bacteria controls DNA repair and outer membrane integrity.

机构信息

Institute of Microbiology and Infection, School of Biosciences, University of Birmingham, Edgbaston, Birmingham, B15 2TT, UK.

Antimicrobials Research Group, Institute of Microbiology and Infection, College of Medical and Dental Sciences, University of Birmingham, Edgbaston, Birmingham, B15 2TT, UK.

出版信息

Nat Commun. 2017 Nov 13;8(1):1444. doi: 10.1038/s41467-017-01405-7.

Abstract

The multiple antibiotic resistance (mar) operon of Escherichia coli is a paradigm for chromosomally encoded antibiotic resistance in enteric bacteria. The locus is recognised for its ability to modulate efflux pump and porin expression via two encoded transcription factors, MarR and MarA. Here we map binding of these regulators across the E. coli genome and identify an extensive mar regulon. Most notably, MarA activates expression of genes required for DNA repair and lipid trafficking. Consequently, the mar locus reduces quinolone-induced DNA damage and the ability of tetracyclines to traverse the outer membrane. These previously unrecognised mar pathways reside within a core regulon, shared by most enteric bacteria. Hence, we provide a framework for understanding multidrug resistance, mediated by analogous systems, across the Enterobacteriaceae. Transcription factors MarR and MarA confer multidrug resistance in enteric bacteria by modulating efflux pump and porin expression. Here, Sharma et al. show that MarA also upregulates genes required for lipid trafficking and DNA repair, thus reducing antibiotic entry and quinolone-induced DNA damage.

摘要

大肠杆菌的多药耐药(mar)操纵子是肠细菌中染色体编码抗生素耐药性的典范。该基因座因其能够通过两个编码转录因子 MarR 和 MarA 调节外排泵和孔蛋白表达而被识别。在这里,我们绘制了这些调节剂在整个大肠杆菌基因组上的结合图谱,并鉴定出一个广泛的 mar 调控子。最值得注意的是,MarA 激活了 DNA 修复和脂质转运所需基因的表达。因此,mar 基因座减少了喹诺酮类药物引起的 DNA 损伤和四环素穿过外膜的能力。这些以前未被识别的 mar 途径位于大多数肠细菌共享的核心调控子内。因此,我们提供了一个框架,用于理解由类似系统介导的整个肠杆菌科的多药耐药性。转录因子 MarR 和 MarA 通过调节外排泵和孔蛋白表达赋予肠细菌多药耐药性。在这里,Sharma 等人表明 MarA 还上调了脂质转运和 DNA 修复所需的基因,从而减少了抗生素的进入和喹诺酮类药物引起的 DNA 损伤。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9526/5684230/db994409d59f/41467_2017_1405_Fig1_HTML.jpg

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