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首页> 外文期刊>Current Microbiology >RpoE may Promote Flagellar Gene Expression in Salmonella enterica Serovar Typhi Under Hyperosmotic Stress
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RpoE may Promote Flagellar Gene Expression in Salmonella enterica Serovar Typhi Under Hyperosmotic Stress

机译:RpoE可能促进高渗胁迫下肠炎沙门氏菌伤寒鞭毛基因表达

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Salmonella enterica serovar Typhi z66 positive strain contains a fljBA-like operon on a linear plasmid. The operon contains the gene fljB:z66 which encodes the z66 antigen. RpoE is a sigma factor σE that initiates transcription of a series of genes in Escherichia and Salmonella under environmental stresses. To investigate whether the gene fljB:z66 is regulated by RpoE (σE), a rpoE deletion mutant of S. enterica serovar Typhi (ΔrpoE) was prepared in this study. The defective motility of the ΔrpoE was confirmed firstly. Transcriptional expression of flagellar genes was screened using a genomic DNA microarray. Some class-2 and most class-3 flagellar genes were downregulated in the ΔrpoE after 30 min of hyperosmotic stress. The expression of fliA and fljB:z66, a class-2 flagellar gene and a class-3 flagellar gene, obviously decreased; however, expression of the class-1 flagellar genes flhDC did not change obviously in the ΔrpoE compared to the wild-type strain in the same conditions. Results of quantitative real-time PCR (qRT-PCR) showed that the expression levels of fliA and fljB:z66 in the ΔrpoE after 30 min of hyperosmotic stress decreased about five and eightfold, respectively, compared to the wild-type strain. Similar results were observed at 120 min of hyperosmotic stress. Western blotting and qRT-PCR analysis showed that expression of fliA and fljB:z66 was significantly increased after supplemental expression of rpoE with a recombinant plasmid pBADrpoE in the ΔrpoE strain. These results demonstrated that RpoE promoted the expression of class-3 flagellar genes and it might be performed by initiating the expression of fliA in S. enterica serovar Typhi under hyperosmotic stress.
机译:肠炎沙门氏菌鼠伤寒沙门氏菌z66阳性菌株在线性质粒上含有fljBA样操纵子。操纵子包含编码z66抗原的基因fljB:z66。 RpoE是一个西格玛因子σ E ,它在环境胁迫下启动大肠杆菌和沙门氏菌中一系列基因的转录。为了研究fljB:z66基因是否受RpoE(σ E )调控,本文制备了鼠伤寒沙门氏菌Typhi(ΔrpoE)的rpoE缺失突变体。首先证实了ΔrpoE的运动能力不良。使用基因组DNA微阵列筛选鞭毛基因的转录表达。高渗胁迫30分钟后,一些2类和大多数3类鞭毛基因在ΔrpoE中被下调。 2级鞭毛基因和3级鞭毛基因fliA和fljB:z66的表达明显降低;然而,在相同条件下,与野生型菌株相比,ΔrpoE中的1类鞭毛基因flhDC的表达没有明显改变。实时定量PCR(qRT-PCR)结果表明,高渗胁迫30分钟后,ΔrpoE中fliA和fljB:z66的表达水平与野生型菌株相比分别降低了约5倍和8倍。在高渗应激120分钟时观察到相似的结果。 Western印迹和qRT-PCR分析表明,在ΔrpoE菌株中补充重组质粒pBADrpoE的rpoE补充表达后,fliA和fljB:z66的表达显着增加。这些结果表明,RpoE促进了3类鞭毛基因的表达,可能是通过在高渗胁迫下通过启动fliA在肠炎沙门氏菌血清型中的表达来实现的。

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