Université Paris Diderot, Sorbonne Paris Cité, EA3105, Paris, France.
J Bacteriol. 2014 Apr;196(7):1343-9. doi: 10.1128/JB.01153-13. Epub 2014 Jan 17.
The ability to capture iron is a challenge for most bacteria. The neonatal meningitis Escherichia coli strain S88 possesses several iron uptake systems, notably including siderophores. Transcriptional analysis of the ColV plasmid pS88 has shown strong induction of a previously undescribed gene with low identity to three E. coli chromosomal genes encoding phospho-2-dehydro-3-deoxyheptonate aldolases involved in aromatic amino acid and catecholate/phenolate siderophore biosynthesis through the shikimate pathway. Here, we investigated the role of this gene, ssbLp (ssbL carried on the plasmid), in siderophore biosynthesis and, consequently, in S88 virulence. We constructed an S88 mutant designated S88 ΔssbLp, which exhibited reduced growth under low-iron conditions compared to the wild-type strain. Liquid chromatography-mass spectroscopy analysis of culture supernatants showed that the mutant secreted significantly smaller amounts of enterobactin, salmochelin SX, and yersiniabactin than the wild-type strain. The mutant was also less virulent in a neonatal rat sepsis model, with significantly lower bacteremia and mortality. Supplementation with chorismate, the final product of the shikimate pathway, restored the wild-type phenotype in vitro. In a collection of human extraintestinal E. coli isolates, we found that ssbL was present only in strains harboring the iro locus, encoding salmochelins, and was located either on the chromosome or on plasmids. Acquisition of the iro locus has been accompanied by acquisition of the auxiliary gene ssbL, which boosts the metabolic pathway essential for catecholate/phenolate siderophore biosynthesis and could represent potential therapeutic targets.
大多数细菌获取铁的能力都是一项挑战。新生儿脑膜炎大肠杆菌 S88 株拥有多种铁摄取系统,尤其是包括铁载体。ColV 质粒 pS88 的转录分析显示,一个以前未描述的基因强烈诱导,该基因与编码参与芳香族氨基酸和儿茶酚/酚酸盐铁载体生物合成的磷酸-2-去氢-3-脱氧庚酮醛缩酶的三个大肠杆菌染色体基因的低同一性。在这里,我们研究了这个基因 ssbLp(质粒上的 ssbL)在铁载体生物合成中的作用,以及由此对 S88 毒力的影响。我们构建了一个 S88 突变体,命名为 S88ΔssbLp,与野生型菌株相比,该突变体在低铁条件下的生长受到显著抑制。培养上清液的液相色谱-质谱分析表明,突变体分泌的肠杆菌素、水杨醇 SX 和耶尔森菌素的量明显少于野生型菌株。突变体在新生大鼠败血病模型中的毒力也较低,菌血症和死亡率明显降低。补充莽草酸,即莽草酸途径的最终产物,可在体外恢复野生型表型。在一组人肠外大肠杆菌分离株中,我们发现 ssbL 仅存在于携带 iro 基因座的菌株中,该基因座编码水杨醇,位于染色体或质粒上。iro 基因座的获得伴随着辅助基因 ssbL 的获得,该基因增强了儿茶酚/酚酸盐铁载体生物合成所必需的代谢途径,这可能代表潜在的治疗靶点。