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细菌抑制 RNA 聚合酶 II 依赖性宿主基因表达。

Bacterial Suppression of RNA Polymerase II-Dependent Host Gene Expression.

机构信息

Department of Microbiology, Immunology and Glycobiology, Institute of Laboratory Medicine, Lund University, 22184 Lund, Sweden.

Institute of Hygiene, University Hospital Münster, Westfälische Wilhelms-Universität, 48149 Münster, Germany.

出版信息

Pathogens. 2016 Jul 13;5(3):49. doi: 10.3390/pathogens5030049.

Abstract

Asymptomatic bacteriuria (ABU) is a bacterial carrier state in the urinary tract that resembles commensalism at other mucosal sites. ABU strains often lack the virulence factors that characterize uropathogenic Escherichia coli (E. coli) strains and therefore elicit weak innate immune responses in the urinary tract. In addition, ABU strains are active modifiers of the host environment, which they influence by suppressing RNA polymerase II (Pol II)-dependent host gene expression. In patients inoculated with the ABU strain E. coli 83972, gene expression was markedly reduced after 24 h (>60% of all regulated genes). Specific repressors and activators of Pol II-dependent transcription were modified, and Pol II Serine 2 phosphorylation was significantly inhibited, indicating reduced activity of the polymerase. This active inhibition included disease-associated innate immune response pathways, defined by TLR4, IRF-3 and IRF-7, suggesting that ABU strains persist in human hosts by active suppression of the antibacterial defense. In a search for the mechanism of inhibition, we compared the whole genome sequences of E. coli 83972 and the uropathogenic strain E. coli CFT073. In addition to the known loss of virulence genes, we observed that the ABU strain has acquired several phages and identified the lytic Prophage 3 as a candidate Pol II inhibitor. Intact phage particles were released by ABU during in vitro growth in human urine. To address if Prophage 3 affects Pol II activity, we constructed a Prophage 3 negative deletion mutant in E. coli 83972 and compared the effect on Pol II phosphorylation between the mutant and the E. coli 83972 wild type (WT) strains. No difference was detected, suggesting that the Pol II inhibitor is not encoded by the phage. The review summarizes the evidence that the ABU strain E. coli 83972 modifies host gene expression by inhibition of Pol II phosphorylation, and discusses the ability of ABU strains to actively create an environment that enhances their persistence.

摘要

无症状菌尿症(ABU)是一种在尿路中的细菌携带状态,类似于其他黏膜部位的共生状态。ABU 菌株通常缺乏尿路致病性大肠杆菌(E. coli)菌株所具有的毒力因子,因此在尿路中引发较弱的先天免疫反应。此外,ABU 菌株是宿主环境的积极修饰者,通过抑制 RNA 聚合酶 II(Pol II)依赖性宿主基因表达来影响宿主环境。在接种 ABU 菌株 E. coli 83972 的患者中,24 小时后(所有受调控基因的>60%)基因表达明显降低。Pol II 依赖性转录的特定抑制剂和激活剂被修饰,Pol II 丝氨酸 2 磷酸化受到显著抑制,表明聚合酶活性降低。这种主动抑制包括 TLR4、IRF-3 和 IRF-7 定义的与疾病相关的先天免疫反应途径,表明 ABU 菌株通过主动抑制抗菌防御在人类宿主中持续存在。在寻找抑制机制的过程中,我们比较了 E. coli 83972 和尿路致病性菌株 E. coli CFT073 的全基因组序列。除了已知的毒力基因丢失外,我们还观察到 ABU 菌株获得了几个噬菌体,并鉴定出裂解性 Prophage 3 是 Pol II 抑制剂的候选物。ABU 在人尿体外生长过程中释放完整的噬菌体颗粒。为了确定 Prophage 3 是否影响 Pol II 活性,我们在 E. coli 83972 中构建了一个 Prophage 3 阴性缺失突变体,并比较了突变体和 E. coli 83972 野生型(WT)菌株之间 Pol II 磷酸化的差异。未检测到差异,表明 Pol II 抑制剂不是由噬菌体编码的。该综述总结了 ABU 菌株 E. coli 83972 通过抑制 Pol II 磷酸化修饰宿主基因表达的证据,并讨论了 ABU 菌株主动创造增强其持久性的环境的能力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e637/5039429/47c95136628c/pathogens-05-00049-g001.jpg

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