Bibi-Triki Sabrina, Li de la Sierra-Gallay Inès, Lazar Noureddine, Leroy Arnaud, Van Tilbeurgh Herman, Sebbane Florent, Pradel Elizabeth
Equipe Peste et Yersinia pestis, INSERM U1019, Lille, France CNRS UMR 8204, Lille, France Institut Pasteur de Lille, Centre d'Infection et d'Immunité, Lille, France Université Lille Nord de France, Lille, France UDSL, Lille, France.
Equipe Fonction et Architecture des Assemblages MacroMoléculaires, IBBMC, Université Paris-Sud, CNRS UMR 8619, Orsay, France.
J Bacteriol. 2014 Nov;196(21):3712-23. doi: 10.1128/JB.01932-14. Epub 2014 Aug 11.
The mechanisms involved in the virulence of Yersinia pestis, the plague pathogen, are not fully understood. In previous research, we found that a Y. pestis mutant lacking the HicB3 (YPO3369) putative orphan antitoxin was attenuated for virulence in a murine model of bubonic plague. Toxin-antitoxin systems (TASs) are widespread in prokaryotes. Most bacterial species possess many TASs of several types. In type II TASs, the toxin protein is bound and neutralized by its cognate antitoxin protein in the cytoplasm. Here we identify the hicA3 gene encoding the toxin neutralized by HicB3 and show that HicA3-HicB3 constitutes a new functional type II TAS in Y. pestis. Using biochemical and mutagenesis-based approaches, we demonstrate that the HicA3 toxin is an RNase with a catalytic histidine residue. HicB3 has two functions: it sequesters and neutralizes HicA3 by blocking its active site, and it represses transcription of the hicA3B3 operon. Gel shift assays and reporter fusion experiments indicate that the HicB3 antitoxin binds to two operators in the hicA3B3 promoter region. We solved the X-ray structures of HicB3 and the HicA3-HicB3 complex; thus, we present the first crystal structure of a TA complex from the HicAB family. HicB3 forms a tetramer that can bind two HicA3 toxin molecules. HicA3 is monomeric and folds as a double-stranded-RNA-binding domain. The HicB3 N-terminal domain occludes the HicA3 active site, whereas its C-terminal domain folds as a ribbon-helix-helix DNA-binding motif.
鼠疫病原体鼠疫耶尔森菌的毒力相关机制尚未完全明确。在之前的研究中,我们发现缺失假定孤儿抗毒素HicB3(YPO3369)的鼠疫耶尔森菌突变体在腺鼠疫小鼠模型中的毒力减弱。毒素-抗毒素系统(TASs)在原核生物中广泛存在。大多数细菌物种拥有多种类型的多个TASs。在II型TASs中,毒素蛋白在细胞质中被其同源抗毒素蛋白结合并中和。在此,我们鉴定出编码被HicB3中和的毒素的hicA3基因,并表明HicA3-HicB3在鼠疫耶尔森菌中构成一种新的功能性II型TAS。使用基于生化和诱变的方法,我们证明HicA3毒素是一种具有催化组氨酸残基的核糖核酸酶。HicB3具有两种功能:它通过阻断HicA3的活性位点来隔离并中和HicA3,并且它抑制hicA3B3操纵子的转录。凝胶迁移实验和报告基因融合实验表明,HicB3抗毒素与hicA3B3启动子区域的两个操纵子结合。我们解析了HicB3和HicA3-HicB3复合物的X射线结构;因此,我们展示了来自HicAB家族的TA复合物的首个晶体结构。HicB3形成一个可以结合两个HicA3毒素分子的四聚体。HicA3是单体,折叠成双链RNA结合结构域。HicB3的N端结构域封闭HicA3的活性位点,而其C端结构域折叠成带状-螺旋-螺旋DNA结合基序。