Gu Dan, Liu Huan, Yang Zhen, Zhang Yuanxing, Wang Qiyao
State Key Laboratory of Bioreactor Engineering, East China University of Science and Technology, Shanghai, China.
School of Food and Biological Engineering, Shaanxi University of Science and Technology, Xi'an, China.
J Bacteriol. 2016 Oct 7;198(21):2985-2999. doi: 10.1128/JB.00520-16. Print 2016 Nov 1.
Quorum sensing (QS) is an important regulatory system in virulence expression and environmental adaptation in bacteria. The master QS regulators (MQSR) LuxR and AphA reciprocally control QS gene expression in vibrios. However, the molecular basis for the regulatory functions of AphA remains undefined. In this study, we characterized its regulatory roles in Vibrio alginolyticus, an important zoonotic pathogen causing diseases in marine animals as well as in humans. AphA is involved in the motility ability, biofilm formation, and in vivo survival of V. alginolyticus Specifically, AphA is expressed at low-cell-density growth phases. In addition, AphA negatively regulates the expression of the main virulence factor, alkaline serine protease (Asp), through LuxR. Chromatin immunoprecipitation (ChIP) followed by high-throughput DNA sequencing (ChIP-seq) detected 49 enriched loci harboring AphA-binding peaks across the V. alginolyticus genome. An AphA-specific binding motif was identified and further confirmed by electrophoretic mobility shift assay (EMSA) and mutagenesis analysis. A quantitative real-time PCR (qRT-PCR) assay further validated the regulation of AphA on these genes. AphA binds directly to the aphA promoter and negatively regulates its own expression. Moreover, AphA directly regulates genes encoding adenylate cyclase, anti-σ, FabR, and the small RNA CsrB, revealing versatile regulatory roles of AphA in its physiology and virulence. Furthermore, our data indicated that AphA modulates motility through the coordinated function of LuxR and CsrB. Collectively, the findings of this work contribute to better understanding of the regulatory roles of AphA in QS and non-QS genes.
In this work, we determined that AphA, the master regulator of QS at low cell density, plays essential roles in expression of genes associated with physiology and virulence in V. alginolyticus, a Gram-negative pathogen for humans and marine animals. We further uncovered that 49 genes could be directly regulated by AphA and a 19-bp consensus binding sequence was identified. Among the 49 genes, the QS and other non-QS-associated genes were identified to be regulated by AphA. Besides, the small RNA CsrB was negatively regulated by AphA, and AphA regulate motility abilities through both CsrB and LuxR. Taken together, the findings of this study improve our understanding of the complex regulation network of AphA and QS.
群体感应(QS)是细菌毒力表达和环境适应中的一种重要调控系统。主要的群体感应调节因子(MQSR)LuxR和AphA相互控制弧菌中的群体感应基因表达。然而,AphA调控功能的分子基础仍不明确。在本研究中,我们表征了其在溶藻弧菌中的调控作用,溶藻弧菌是一种重要的人畜共患病原体,可导致海洋动物以及人类患病。AphA参与溶藻弧菌的运动能力、生物膜形成和体内存活。具体而言,AphA在低细胞密度生长阶段表达。此外,AphA通过LuxR负调控主要毒力因子碱性丝氨酸蛋白酶(Asp)的表达。染色质免疫沉淀(ChIP)结合高通量DNA测序(ChIP-seq)在溶藻弧菌基因组中检测到49个富含AphA结合峰的位点。鉴定出一个AphA特异性结合基序,并通过电泳迁移率变动分析(EMSA)和诱变分析进一步证实。定量实时PCR(qRT-PCR)分析进一步验证了AphA对这些基因的调控。AphA直接结合aphA启动子并负调控其自身表达。此外,AphA直接调控编码腺苷酸环化酶、抗σ因子、FabR和小RNA CsrB的基因,揭示了AphA在其生理和毒力方面的多种调控作用。此外,我们的数据表明AphA通过LuxR和CsrB的协同作用调节运动能力。总的来说,这项工作的发现有助于更好地理解AphA在群体感应和非群体感应基因中的调控作用。
在本研究中,我们确定低细胞密度群体感应的主要调节因子AphA在溶藻弧菌(一种对人类和海洋动物致病的革兰氏阴性病原体)中与生理和毒力相关的基因表达中起重要作用。我们进一步发现49个基因可被AphA直接调控,并鉴定出一个19 bp的共有结合序列。在这49个基因中,群体感应和其他非群体感应相关基因被鉴定为受AphA调控。此外,小RNA CsrB受AphA负调控,并且AphA通过CsrB和LuxR调节运动能力。综上所述,本研究的发现增进了我们对AphA和群体感应复杂调控网络的理解。