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铜绿假单胞菌中藻酸盐操纵子的转录受 c-di-GMP 调控。

Transcription of the Alginate Operon in Pseudomonas aeruginosa Is Regulated by c-di-GMP.

机构信息

Costerton Biofilm Center, Department of Immunology and Microbiology, Faculty of Health and Medical Sciences, University of Copenhagengrid.5254.6, Copenhagen, Denmark.

Department of Biology, Copenhagen Biocenter, University of Copenhagengrid.5254.6, Copenhagen, Denmark.

出版信息

Microbiol Spectr. 2022 Aug 31;10(4):e0067522. doi: 10.1128/spectrum.00675-22. Epub 2022 Jul 11.

Abstract

Overproduction of the exopolysaccharide alginate contributes to the pathogenicity and antibiotic tolerance of Pseudomonas aeruginosa in chronic infections. The second messenger, c-di-GMP, is a positive regulator of the production of various biofilm matrix components and is known to regulate alginate synthesis at the posttranslational level in P. aeruginosa. We provide evidence that c-di-GMP also regulates transcription of the alginate operon in P. aeruginosa. Previous work has shown that transcription of the alginate operon is regulated by nine different proteins, AmrZ, AlgP, IHFα, IHFβ, CysB, Vfr, AlgR, AlgB, and AlgQ, and we investigated if some of these proteins function as a c-di-GMP effector. We found that deletion of , , , and had only a marginal effect on the transcription of the alginate operon. Deletion of and led to decreased transcription of the alginate operon, and the dependence of the c-di-GMP level was less pronounced, indicating that Vfr and CysB could be partially required for c-di-GMP-mediated regulation of alginate operon transcription. Our experiments indicated that the AmrZ, AlgR, and AlgB proteins are absolutely required for transcription of the alginate operon. However, differential radial capillary action of ligand assay (DRaCALA) and site-directed mutagenesis indicated that c-di-GMP does not bind to any of the AmrZ, AlgR, and AlgB proteins. The proliferation of alginate-overproducing P. aeruginosa variants in the lungs of cystic fibrosis patients often leads to chronic infection. The alginate functions as a biofilm matrix that protects the bacteria against host immune defenses and antibiotic treatment. Knowledge about the regulation of alginate synthesis is important in order to identify drug targets for the development of medicine against chronic P. aeruginosa infections. We provide evidence that c-di-GMP positively regulates transcription of the alginate operon in P. aeruginosa. Moreover, we revisited the role of the known alginate regulators, AmrZ, AlgP, IHFα, IHFβ, CysB, Vfr, AlgR, AlgB, and AlgQ, and found that their effect on transcription of the alginate operon is highly varied. Deletion of , , , or only had a marginal effect on transcription of the alginate operon, whereas deletion of or led to decreased transcription and deletion of , , or abrogated transcription.

摘要

多糖海藻酸盐的过度产生有助于铜绿假单胞菌在慢性感染中的致病性和抗生素耐药性。第二信使 c-di-GMP 是各种生物膜基质成分产生的正调节剂,已知其在铜绿假单胞菌中通过翻译后水平调节海藻酸盐的合成。我们提供的证据表明,c-di-GMP 还调节铜绿假单胞菌中藻酸盐操纵子的转录。先前的工作表明,藻酸盐操纵子的转录受 AmrZ、AlgP、IHFα、IHFβ、CysB、Vfr、AlgR、AlgB 和 AlgQ 等 9 种不同蛋白质的调节,我们研究了这些蛋白质中的一些是否作为 c-di-GMP 效应物发挥作用。我们发现,algT、algQ、algW 和 algZ 的缺失仅对藻酸盐操纵子的转录有轻微影响。algV 和 cysB 的缺失导致藻酸盐操纵子转录减少,对 c-di-GMP 水平的依赖性不明显,表明 Vfr 和 CysB 可能部分需要 c-di-GMP 介导的藻酸盐操纵子转录调节。我们的实验表明,AmrZ、AlgR 和 AlgB 蛋白绝对需要藻酸盐操纵子的转录。然而,配体差示径向毛细管作用分析(DRaCALA)和定点突变实验表明,c-di-GMP 不与任何 AmrZ、AlgR 和 AlgB 蛋白结合。在囊性纤维化患者的肺部,过度产生藻酸盐的铜绿假单胞菌变种的增殖常常导致慢性感染。藻酸盐作为生物膜基质,可保护细菌免受宿主免疫防御和抗生素治疗的影响。了解藻酸盐合成的调节对于确定针对慢性铜绿假单胞菌感染的药物靶点非常重要。我们提供的证据表明,c-di-GMP 正向调节铜绿假单胞菌中藻酸盐操纵子的转录。此外,我们重新研究了已知的藻酸盐调节剂 AmrZ、AlgP、IHFα、IHFβ、CysB、Vfr、AlgR、AlgB 和 AlgQ 的作用,发现它们对藻酸盐操纵子转录的影响差异很大。algT、algQ、algW 或 algZ 的缺失仅对藻酸盐操纵子的转录有轻微影响,而 algV 或 cysB 的缺失导致转录减少,algV、algT、algQ 或 algZ 的缺失则阻断转录。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6476/9431422/0d759e8ff7f8/spectrum.00675-22-f001.jpg

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