CarSR双组分系统直接控制radD的表达,作为一种全局调节剂,在核梭杆菌中感知细菌共聚集。

IF 2.7 3区 生物学 Q3 MICROBIOLOGY
Bibek G C, Chenggang Wu
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引用次数: 0

摘要

双组分系统(TCS)使细菌能够感知和响应环境信号,促进快速适应。RNA-Seq分析显示,口腔关键病原体核梭杆菌(Fusobacterium nucleatum)利用CarSR TCS通过调节编码表面粘附蛋白radD的表达,来调节与各种革兰氏阳性伙伴的共聚集。然而,应答调控子CarR、更广泛的CarR调控子以及该系统感知的信号对含rad操纵子(radABCD)的直接调控尚不清楚。在这项研究中,染色质免疫沉淀和高通量DNA测序(ChIP-seq)在基因组中鉴定了大约161个carr富集位点和一个17 bp的共识基序,可能是carr结合位点。值得注意的是,在radABCD操纵子的启动子区域发现了一个这样的结合基序。CarR与这个结合基序的相互作用通过电泳迁移率转移分析、诱变和dna酶I足迹分析得到进一步验证。除了调节radABCD外,CarR还直接控制与果糖和氨基酸(半胱氨酸、谷氨酸、赖氨酸)利用有关的基因,强调了其在F. nucleatum中作为全局调节剂的作用。最后,我们发现radD介导的共聚集增强了radD的表达,而car的缺失消除了这种增强,这表明共聚集本身是TCS感知的信号。这些发现为研究CarR调控和RadD调控提供了新的见解,阐明了具核梭菌在牙菌斑形成和疾病过程中的生态和致病作用。重要意义核杆菌是口腔生物膜的重要成员,作为连接早期和晚期定殖菌的桥接生物,从而推动牙菌斑的形成。它与不同细菌伙伴聚集的非凡能力是其生态成功的核心,但它感知和响应这些相互作用的机制仍然知之甚少。本研究确定了CarSR双组分系统是介导共聚集的主要粘附素RadD的直接调节剂,并揭示了其作为信号感知共聚集的作用。这些发现揭示了具核梭菌动态适应多种微生物环境的新机制,为研究复杂口腔微生物生态系统中生物膜的形成和细菌交流提供了新的视角。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The CarSR two-component system directly controls radD expression as a global regulator that senses bacterial coaggregation in Fusobacterium nucleatum.

Two-component systems (TCS) enable bacteria to sense and respond to environmental signals, facilitating rapid adaptation. Fusobacterium nucleatum, a key oral pathobiont, employs the CarSR TCS to modulate coaggregation with various gram-positive partners by regulating the expression of radD, encoding a surface adhesion protein, as revealed by RNA-Seq analysis. However, the direct regulation of the radD-containing operon (radABCD) by the response regulator CarR, the broader CarR regulon, and the signals sensed by this system remain unclear. In this study, chromatin immunoprecipitation followed by high-throughput DNA sequencing (ChIP-seq) identified approximately 161 CarR-enriched loci across the genome and a 17 bp consensus motif that likely serves as the CarR-binding site. Notably, one such binding motif was found in the promoter region of the radABCD operon. The interaction of CarR with this binding motif was further validated using electrophoretic mobility shift assays, mutagenesis, and DNase I footprinting analyses. Beyond regulating radABCD, CarR directly controls genes involved in fructose and amino acid (cysteine, glutamate, lysine) utilization, underscoring its role as a global regulator in F. nucleatum. Lastly, we discovered that RadD-mediated coaggregation enhances radD expression, and deletion of carS abolished this enhancement, suggesting that coaggregation itself serves as a signal sensed by this TCS. These findings provide new insights into the CarR regulon and the regulation of RadD, elucidating the ecological and pathogenic roles of F. nucleatum in dental plaque formation and disease processes.IMPORTANCEFusobacterium nucleatum is an essential member of oral biofilms acting as a bridging organism that connects early and late colonizers, thus driving dental plaque formation. Its remarkable ability to aggregate with diverse bacterial partners is central to its ecological success, yet the mechanisms it senses and responds to these interactions remain poorly understood. This study identifies the CarSR two-component system as a direct regulator of RadD, a major adhesin mediating coaggregation, and reveals its role in sensing coaggregation as a signal. These findings uncover a novel mechanism by which F. nucleatum dynamically adapts to polymicrobial environments, offering new perspectives on biofilm formation and bacterial communication in complex oral microbial ecosystems.

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来源期刊
Journal of Bacteriology
Journal of Bacteriology 生物-微生物学
CiteScore
6.10
自引率
9.40%
发文量
324
审稿时长
1.3 months
期刊介绍: The Journal of Bacteriology (JB) publishes research articles that probe fundamental processes in bacteria, archaea and their viruses, and the molecular mechanisms by which they interact with each other and with their hosts and their environments.
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