Department of Biochemistry and Molecular Biology, School of Medical Technology, Jiangsu University, Zhenjiang, China.
Curr Microbiol. 2011 Feb;62(2):492-500. doi: 10.1007/s00284-010-9734-y. Epub 2010 Aug 18.
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 σ(E) 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 (σ(E)), 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.
肠炎沙门氏菌 Typhi z66 阳性菌株在线性质粒上含有一个 fljBA 样操纵子。该操纵子包含基因 fljB:z66,其编码 z66 抗原。RpoE 是一种 σ(E)因子,在环境应激下,它启动大肠杆菌和沙门氏菌中一系列基因的转录。为了研究基因 fljB:z66 是否受 RpoE(σ(E))调控,本研究制备了肠炎沙门氏菌 Typhi 的 rpoE 缺失突变体(ΔrpoE)。首先证实了 ΔrpoE 的运动缺陷。使用基因组 DNA 微阵列筛选了鞭毛基因的转录表达。在高渗应激 30 分钟后,ΔrpoE 中一些 2 类和大多数 3 类鞭毛基因的转录表达下调。2 类鞭毛基因 fliA 和 3 类鞭毛基因 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 1 类鞭毛基因 flhDC 的表达没有明显变化。定量实时 PCR(qRT-PCR)结果显示,在高渗应激 30 分钟后,ΔrpoE 中 fliA 和 fljB:z66 的表达水平分别比野生型菌株降低了约 5 倍和 8 倍。在高渗应激 120 分钟时也观察到类似的结果。Western 印迹和 qRT-PCR 分析表明,在ΔrpoE 菌株中,用重组质粒 pBADrpoE 补充表达 rpoE 后,fliA 和 fljB:z66 的表达显著增加。这些结果表明,RpoE 在高渗应激下促进了 3 类鞭毛基因的表达,它可能通过启动 Typhi 中的 fliA 表达来实现。