Suppr超能文献

铜绿假单胞菌AlgR通过激活fimU-pilVWXY1Y2E操纵子的转录来调控IV型菌毛的生物合成。

Pseudomonas aeruginosa AlgR regulates type IV pilus biosynthesis by activating transcription of the fimU-pilVWXY1Y2E operon.

作者信息

Belete Belen, Lu Haiping, Wozniak Daniel J

机构信息

Department of Microbiology and Immunology, Wake Forest University School of Medicine, Medical Center Blvd., Winston-Salem, NC 27157-1064, USA.

出版信息

J Bacteriol. 2008 Mar;190(6):2023-30. doi: 10.1128/JB.01623-07. Epub 2008 Jan 4.

Abstract

The response regulator AlgR is required for Pseudomonas aeruginosa type IV pilus-dependent twitching motility, a flagellum-independent mode of solid surface translocation. Prior work showed that AlgR is phosphorylated at aspartate 54, and cells expressing an AlgR variant that cannot undergo phosphorylation (AlgRD54N) lack twitching motility. However, the mechanism by which AlgR controls twitching motility is not completely understood. We hypothesized that AlgR functioned by activating genes within the prepilin fimU-pilVWXY1Y2E cluster that are necessary for type IV pilin biogenesis. Reverse transcriptase PCR analysis showed that the fimU-pilVWXY1Y2E genes are cotranscribed in an operon, which is under the control of AlgR. This supports prior transcriptional profiling studies of wild-type strains and algR mutants. Moreover, expression of the fimU-pilVWXY1Y2E operon was reduced in strains expressing AlgRD54N. DNase footprinting and electrophoretic mobility shift assays demonstrate that AlgR but not AlgRD54N bound with high affinity to two sites upstream of the fimU-pilVWXY1Y2E operon. Altogether, our findings indicate that AlgR is essential for proper pilin localization and that phosphorylation of AlgR results in direct activation of the fimU-pilVWXY1Y2E operon, which is required for the assembly and export of a functional type IV pilus.

摘要

响应调节因子AlgR是铜绿假单胞菌IV型菌毛依赖性颤动运动所必需的,这是一种不依赖鞭毛的固体表面移位模式。先前的研究表明,AlgR在天冬氨酸54处被磷酸化,表达不能进行磷酸化的AlgR变体(AlgRD54N)的细胞缺乏颤动运动。然而,AlgR控制颤动运动的机制尚未完全了解。我们推测AlgR通过激活前菌毛素fimU-pilVWXY1Y2E簇内对IV型菌毛生物合成必需的基因来发挥作用。逆转录酶PCR分析表明,fimU-pilVWXY1Y2E基因在一个操纵子中共同转录,该操纵子受AlgR的控制。这支持了对野生型菌株和algR突变体的先前转录谱研究。此外,在表达AlgRD54N的菌株中,fimU-pilVWXY1Y2E操纵子的表达降低。DNA酶足迹法和电泳迁移率变动分析表明,AlgR而非AlgRD54N以高亲和力结合到fimU-pilVWXY1Y2E操纵子上游的两个位点。总之,我们的研究结果表明,AlgR对于菌毛素的正确定位至关重要,并且AlgR的磷酸化导致fimU-pilVWXY1Y2E操纵子的直接激活,这是功能性IV型菌毛组装和输出所必需的。

相似文献

2
Identification of AlgR-regulated genes in Pseudomonas aeruginosa by use of microarray analysis.
J Bacteriol. 2004 Sep;186(17):5672-84. doi: 10.1128/JB.186.17.5672-5684.2004.
3
Global Regulatory Pathways Converge To Control Expression of Pseudomonas aeruginosa Type IV Pili.
mBio. 2022 Feb 22;13(1):e0369621. doi: 10.1128/mbio.03696-21. Epub 2022 Jan 25.
4
Pseudomonas aeruginosa type IV minor pilins and PilY1 regulate virulence by modulating FimS-AlgR activity.
PLoS Pathog. 2018 May 18;14(5):e1007074. doi: 10.1371/journal.ppat.1007074. eCollection 2018 May.
5
Pseudomonas aeruginosa AlgR phosphorylation modulates rhamnolipid production and motility.
J Bacteriol. 2013 Dec;195(24):5499-515. doi: 10.1128/JB.00726-13. Epub 2013 Oct 4.
7
Pseudomonas aeruginosa AlgR represses the Rhl quorum-sensing system in a biofilm-specific manner.
J Bacteriol. 2007 Nov;189(21):7752-64. doi: 10.1128/JB.01797-06. Epub 2007 Aug 31.
8
Pseudomonas aeruginosa minor pilins are incorporated into type IV pili.
J Mol Biol. 2010 May 7;398(3):444-61. doi: 10.1016/j.jmb.2010.03.028. Epub 2010 Mar 23.
10
AlgR Phosphorylation Status Differentially Regulates Pyocyanin and Pyoverdine Production.
mBio. 2018 Jan 30;9(1):e02318-17. doi: 10.1128/mBio.02318-17.

引用本文的文献

1
Ser/Thr protein kinase Stk1 phosphorylates the key transcriptional regulator AlgR to modulate virulence and resistance in .
Virulence. 2024 Dec;15(1):2367649. doi: 10.1080/21505594.2024.2367649. Epub 2024 Jun 20.
3
Nonmotile Subpopulations of Repress Flagellar Motility in Motile Cells through a Type IV Pilus- and Pel-Dependent Mechanism.
J Bacteriol. 2022 May 17;204(5):e0052821. doi: 10.1128/jb.00528-21. Epub 2022 Apr 4.
4
The molecular basis of FimT-mediated DNA uptake during bacterial natural transformation.
Nat Commun. 2022 Mar 4;13(1):1065. doi: 10.1038/s41467-022-28690-1.
5
Global Regulatory Pathways Converge To Control Expression of Pseudomonas aeruginosa Type IV Pili.
mBio. 2022 Feb 22;13(1):e0369621. doi: 10.1128/mbio.03696-21. Epub 2022 Jan 25.
6
Impacts of Ser/Thr Protein Kinase Stk1 on the Proteome, Twitching Motility, and Competitive Advantage in .
Front Microbiol. 2021 Sep 22;12:738690. doi: 10.3389/fmicb.2021.738690. eCollection 2021.
9
Hfq-Assisted RsmA Regulation Is Central to Biofilm Polysaccharide PEL Expression.
Front Microbiol. 2020 Nov 17;11:482585. doi: 10.3389/fmicb.2020.482585. eCollection 2020.
10
Cytotoxic alkyl-quinolones mediate surface-induced virulence in Pseudomonas aeruginosa.
PLoS Pathog. 2020 Sep 14;16(9):e1008867. doi: 10.1371/journal.ppat.1008867. eCollection 2020 Sep.

本文引用的文献

1
Binding of Pseudomonas aeruginosa AlgZ to sites upstream of the algZ promoter leads to repression of transcription.
J Bacteriol. 2005 Jul;187(13):4430-43. doi: 10.1128/JB.187.13.4430-4443.2005.
3
MucA-mediated coordination of type III secretion and alginate synthesis in Pseudomonas aeruginosa.
J Bacteriol. 2004 Nov;186(22):7575-85. doi: 10.1128/JB.186.22.7575-7585.2004.
4
Identification of AlgR-regulated genes in Pseudomonas aeruginosa by use of microarray analysis.
J Bacteriol. 2004 Sep;186(17):5672-84. doi: 10.1128/JB.186.17.5672-5684.2004.
5
AlgR functions in algC expression and virulence in Pseudomonas syringae pv. syringae.
Microbiology (Reading). 2004 Aug;150(Pt 8):2727-2737. doi: 10.1099/mic.0.27199-0.
7
Effects of subinhibitory concentrations of macrolide antibiotics on Pseudomonas aeruginosa.
Chest. 2004 Feb;125(2 Suppl):62S-69S; quiz 69S. doi: 10.1378/chest.125.2_suppl.62s.
8
Biofilm formation by Pseudomonas aeruginosa wild type, flagella and type IV pili mutants.
Mol Microbiol. 2003 Jun;48(6):1511-24. doi: 10.1046/j.1365-2958.2003.03525.x.
9
Type II protein secretion in Pseudomonas aeruginosa: the pseudopilus is a multifibrillar and adhesive structure.
J Bacteriol. 2003 May;185(9):2749-58. doi: 10.1128/JB.185.9.2749-2758.2003.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验