首页> 美国卫生研究院文献>The Journal of Biological Chemistry >The Second Type VI Secretion System of Pseudomonas aeruginosa Strain PAO1 Is Regulated by Quorum Sensing and Fur and Modulates Internalization in Epithelial Cells
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The Second Type VI Secretion System of Pseudomonas aeruginosa Strain PAO1 Is Regulated by Quorum Sensing and Fur and Modulates Internalization in Epithelial Cells

机译:铜绿假单胞菌菌株PAO1的第二种VI分泌系统由群体感应和皮毛调节并调节上皮细胞的内在化

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摘要

The genome of Pseudomonas aeruginosa PAO1 contains three type VI secretion systems (T6SSs) called H1-, H2-, and H3-T6SS. The H1-T6SS secretes three identified toxins that target other bacteria, providing a fitness advantage for P. aeruginosa, and likely contributes to bacterial pathogenesis in chronic infections. However, no specific substrates or defined roles have been described for the two other systems. Here, we demonstrate that the expression of H2-T6SS genes of strain PAO1 is up-regulated during the transition from exponential to stationary phase growth and regulated by the Las and Rhl quorum sensing systems. In addition, we identify two putative Fur boxes in the promoter region and find that H2-T6SS transcription is negatively regulated by iron. We also show that the H2-T6SS system enhances bacterial uptake into HeLa cells (75% decrease in internalization with a H2-T6SS mutant) and into lung epithelial cells through a phosphatidylinositol 3-kinase-dependent pathway that induces Akt activation in the host cell (50% decrease in Akt phosphorylation). Finally, we show that H2-T6SS plays a role in P. aeruginosa virulence in the worm model. Thus, in contrast to H1-T6SS, H2-T6SS modulates interaction with eukaryotic host cells. Together, T6SS can carry out different functions that may be important in establishing chronic P. aeruginosa infections in the human host.
机译:铜绿假单胞菌PAO1的基因组包含三个VI型分泌系统(T6SS),分别称为H1-,H2-和H3-T6SS。 H1-T6SS分泌出三种针对其他细菌的毒素,为铜绿假单胞菌提供了健身优势,并可能有助于慢性感染的细菌发病。但是,没有针对其他两个系统描述特定的基材或定义的角色。在这里,我们证明了菌株PAO1的H2-T6SS基因的表达在从指数级到固定相生长的过渡过程中被上调,并由Las和Rhl群体感应系统调节。另外,我们在启动子区域鉴定了两个推定的Fur盒,发现H2-T6SS的转录受铁的负调控。我们还显示,H2-T6SS系统增强了细菌对HeLa细胞的吸收(H2-T6SS突变体的内在化程度降低了75%),并通过磷脂酰肌醇3激酶依赖性途径(其诱导宿主细胞中的Akt活化)进入肺上皮细胞(Akt磷酸化降低50%)。最后,我们表明H2-T6SS在蠕虫模型中在铜绿假单胞菌毒力中起作用。因此,与H1-T6SS相反,H2-T6SS调节与真核宿主细胞的相互作用。 T6SS可以一起执行不同的功能,这对于在人类宿主中建立慢性铜绿假单胞菌感染可能很重要。

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