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RegR是一种全局性的LacI/GalR家族调控因子,可调节肺炎链球菌的毒力和感受态。

RegR, a global LacI/GalR family regulator, modulates virulence and competence in Streptococcus pneumoniae.

作者信息

Chapuy-Regaud Sabine, Ogunniyi A David, Diallo Nicole, Huet Yvette, Desnottes Jean-François, Paton James C, Escaich Sonia, Trombe Marie-Claude

机构信息

Laboratoire Interactions et Signalisation Cellulaire: Relation Hôte Pathogène, Institut Louis Bugnard, Centre Hospitalo-Universitaire de Rangueil, Université Paul Sabatier, 31403 Toulouse Cedex, France.

出版信息

Infect Immun. 2003 May;71(5):2615-25. doi: 10.1128/IAI.71.5.2615-2625.2003.

Abstract

The homolactic and catalase-deficient pathogen Streptococcus pneumoniae is not only tolerant to oxygen but requires the activity of its NADH oxidase, Nox, to develop optimal virulence and competence for genetic transformation. In this work, we show that the global regulator RegR is also involved in these traits. Genetic dissection revealed that RegR regulates competence and the expression of virulence factors, including hyaluronidase. In bacteria grown in vitro, RegR represses hyaluronidase. At neutral pH, it increases adherence to A549 epithelial cells, and at alkaline pH, it acts upstream of the CiaRH two-component signaling system to activate competence. These phenotypes are not associated with changes in antibiotic resistance, central metabolism, and carbohydrate utilization. Although the RegR(0) (where 0 indicates the loss of the protein) mutation is sufficient to attenuate experimental virulence of strain 23477 in mice, the introduction of an additional hyl(0) (where 0 indicates the loss of function) mutation in the RegR(0) strain 23302 dramatically reduces its virulence. This indicates that residual virulence of the RegR(0) Hyl(+) derivative is due to hyaluronidase and supports the dual role of RegR in virulence. This LacI/GalR regulator, not essential for in vitro growth in rich media, is indeed involved in the adaptive response of the pneumococcus via its control of competence, adherence, and virulence.

摘要

缺乏同型乳酸脱氢酶和过氧化氢酶的病原体肺炎链球菌不仅能耐受氧气,还需要其NADH氧化酶Nox的活性来发展最佳毒力和遗传转化能力。在这项研究中,我们表明全局调节因子RegR也参与了这些特性。基因分析表明,RegR调节遗传转化能力和毒力因子的表达,包括透明质酸酶。在体外培养的细菌中,RegR抑制透明质酸酶。在中性pH值下,它增加对A549上皮细胞的黏附,在碱性pH值下,它在CiaRH双组分信号系统上游起作用以激活遗传转化能力。这些表型与抗生素抗性、中心代谢和碳水化合物利用的变化无关。虽然RegR(0)(其中0表示蛋白质缺失)突变足以减弱23477菌株在小鼠中的实验毒力,但在RegR(0)菌株23302中引入额外的hyl(0)(其中0表示功能缺失)突变会显著降低其毒力。这表明RegR(0) Hyl(+)衍生物的残余毒力是由于透明质酸酶,并支持RegR在毒力中的双重作用。这种LacI/GalR调节因子对在丰富培养基中的体外生长不是必需的,它确实通过控制遗传转化能力、黏附和毒力参与肺炎链球菌的适应性反应。

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