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鲍曼不动杆菌双组分系统AdeRS以菌株特异性方式调控多药外排、生物膜形成和毒力所需的基因。

The Acinetobacter baumannii Two-Component System AdeRS Regulates Genes Required for Multidrug Efflux, Biofilm Formation, and Virulence in a Strain-Specific Manner.

作者信息

Richmond Grace E, Evans Laura P, Anderson Michele J, Wand Matthew E, Bonney Laura C, Ivens Alasdair, Chua Kim Lee, Webber Mark A, Sutton J Mark, Peterson Marnie L, Piddock Laura J V

机构信息

Antimicrobial Agents Research Group, Institute of Microbiology and Infection, University of Birmingham, Edgbaston, Birmingham, United Kingdom.

Department of Experimental and Clinical Pharmacology, University of Minnesota, Minneapolis, Minnesota, USA.

出版信息

mBio. 2016 Apr 19;7(2):e00430-16. doi: 10.1128/mBio.00430-16.

Abstract

The opportunistic pathogen Acinetobacter baumannii is able to persist in the environment and is often multidrug resistant (MDR), causing difficulties in the treatment of infections. Here, we show that the two-component system AdeRS, which regulates the production of the AdeABC multidrug resistance efflux pump, is required for the formation of a protective biofilm in an ex vivo porcine mucosal model, which mimics a natural infection of the human epithelium. Interestingly, deletion of adeB impacted only on the ability of strain AYE to form a biofilm on plastic and only on the virulence of strain Singapore 1 for Galleria mellonella RNA-Seq revealed that loss of AdeRS or AdeB significantly altered the transcriptional landscape, resulting in the changed expression of many genes, notably those associated with antimicrobial resistance and virulence interactions. For example, A. baumannii lacking AdeRS displayed decreased expression of adeABC, pil genes, com genes, and a pgaC-like gene, whereas loss of AdeB resulted in increased expression of pil and com genes and decreased expression of ferric acinetobactin transport system genes. These data define the scope of AdeRS-mediated regulation, show that changes in the production of AdeABC mediate important phenotypes controlled by AdeRS, and suggest that AdeABC is a viable target for antimicrobial drug and antibiofilm discovery [corrected].

摘要

机会致病菌鲍曼不动杆菌能够在环境中存活,且常常具有多重耐药性(MDR),这给感染治疗带来了困难。在此,我们表明,调控AdeABC多重耐药性外排泵产生的双组分系统AdeRS,在体外猪黏膜模型中形成保护性生物膜是必需的,该模型模拟了人类上皮细胞的自然感染。有趣的是,adeB的缺失仅影响AYE菌株在塑料上形成生物膜的能力,且仅影响新加坡1菌株对大蜡螟的毒力。RNA测序显示,AdeRS或AdeB的缺失显著改变了转录图谱,导致许多基因的表达发生变化,尤其是那些与抗微生物耐药性和毒力相互作用相关的基因。例如,缺乏AdeRS的鲍曼不动杆菌显示adeABC、菌毛基因、com基因和一个类pgaC基因的表达降低,而AdeB的缺失导致菌毛和com基因的表达增加,铁载体转运系统基因的表达降低。这些数据确定了AdeRS介导的调控范围,表明AdeABC产生的变化介导了由AdeRS控制的重要表型,并表明AdeABC是抗微生物药物和抗生物膜发现的一个可行靶点[已修正]。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b2f4/4850262/72fcb2540568/mbo0021627740001.jpg

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