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首页> 外文期刊>Journal of bacteriology >Role of Histone-Like Proteins H-NS and StpA in Expression of Virulence Determinants of Uropathogenic Escherichia coli
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Role of Histone-Like Proteins H-NS and StpA in Expression of Virulence Determinants of Uropathogenic Escherichia coli

机译:组蛋白样蛋白H-NS和StpA在尿毒原性大肠杆菌毒力决定簇表达中的作用

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摘要

The histone-like protein H-NS is a global regulator in Escherichia coli that has been intensively studied in nonpathogenic strains. However, no comprehensive study on the role of H-NS and its paralogue, StpA, in gene expression in pathogenic E. coli has been carried out so far. Here, we monitored the global effects of H-NS and StpA in a uropathogenic E. coli isolate by using DNA arrays. Expression profiling revealed that more than 500 genes were affected by an hns mutation, whereas no effect of StpA alone was observed. An hns stpA double mutant showed a distinct gene expression pattern that differed in large part from that of the hns single mutant. This suggests a direct interaction between the two paralogues and the existence of distinct regulons of H-NS and an H-NS/StpA heteromeric complex. hns mutation resulted in increased expression of alpha-hemolysin, fimbriae, and iron uptake systems as well as genes involved in stress adaptation. Furthermore, several other putative virulence genes were found to be part of the H-NS regulon. Although the lack of H-NS, either alone or in combination with StpA, has a huge impact on gene expression in pathogenic E. coli strains, its effect on virulence is ambiguous. At a high infection dose, hns mutants trigger more sudden lethality due to their increased acute toxicity in murine urinary tract infection and sepsis models. At a lower infectious dose, however, mutants lacking H-NS are attenuated through their impaired growth rate, which can only partially be compensated for by the higher expression of numerous virulence factors.
机译:组蛋白样蛋白H-NS是大肠杆菌中的一种全球调节物,已在非致病性菌株中进行了深入研究。但是,尚未对H-NS及其旁系同源蛋白StpA在致病性 E基因表达中的作用进行全面研究。到目前为止,已经进行了大肠杆菌。在这里,我们监测了尿毒症 E中H-NS和StpA的总体作用。 DNA阵列分离大肠杆菌。表达谱分析表明, hns 突变影响了500多个基因,而单独观察不到StpA的作用。一个 hns stpA 双重突变体表现出明显的基因表达模式,在很大程度上与 hns 单突变体不同。这暗示了两个旁系同源物之间的直接相互作用以及H-NS和H-NS / StpA异聚复合物的不同调节子的存在。 hns 突变导致α-溶血素,菌毛和铁吸收系统以及与压力适应有关的基因的表达增加。此外,发现其他几个推定的毒力基因是H-NS调节子的一部分。尽管缺乏H-NS,无论是单独使用还是与StpA结合使用,都对致病性 E中的基因表达产生巨大影响。大肠杆菌菌株,其对毒力的作用尚不明确。在高感染剂量下, hns 突变体由于其在鼠尿道感染和败血症模型中增加的急性毒性而触发更多的突然杀伤力。然而,在较低的感染剂量下,缺乏H-NS的突变体会通过其受损的生长速度而减弱,而这些生长速度只能部分地被众多毒力因子的较高表达所补偿。

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