Krause M, Fang F C, Guiney D G
Department of Medicine, UCSD Medical Center 92103.
J Bacteriol. 1992 Jul;174(13):4482-9. doi: 10.1128/jb.174.13.4482-4489.1992.
The 80-kb plasmid pSDL2 of Salmonella dublin Lane is essential for lethal systemic infection in experimental mice. A cluster of five plasmid genes, designated spvR, spvA, spvB, spvC, and spvD, is sufficient to express the plasmid-related virulent phenotype. The spvR gene product has recently been identified as a positive regulator of spvB expression in the stationary phase of bacterial growth (F. C. Fang, M. Krause, C. Roudier, J. Fierer, and D. G. Guiney, J. Bacteriol. 173:6783-6789, 1991). In this study, we evaluated the role of SpvR in the transcription of the downstream virulence genes spvABCD. Analysis of mRNA synthesis revealed that SpvR promotes transcription of the downstream spvABCD genes in the stationary growth phase. Transcript mapping of the spv region demonstrated an unusual operon structure involving messages for spvA, spvAB, spvABC, and spvABCD. Quantitative measurement of transcription and of gene expression by use of translational spv-lacZ fusions suggested that SpvA, SpvB, SpvC, and SpvD are produced in decreasing abundance. Primer extension assays identified two transcriptional start sites 70 and 98 bp upstream of the start codon of spvA, but none upstream of spvB, spvC, or spvD. Deletion of a 320-bp EcoRI-ApaI segment that contains both start sites abolished expression of the downstream spvB and spvC genes. Our results establish a central function of SpvR as a positive regulator of the downstream spvABCD genes in the stationary phase of bacterial growth and indicate that the primary mechanism of regulation is by activation of promoters upstream of spvA.
都柏林沙门氏菌Lane株的80kb质粒pSDL2对于实验小鼠的致死性全身感染至关重要。一组五个质粒基因,命名为spvR、spvA、spvB、spvC和spvD,足以表达与质粒相关的毒力表型。最近已确定spvR基因产物是细菌生长稳定期spvB表达的正调控因子(F.C.方、M.克劳斯、C.鲁迪耶、J.菲勒和D.G.吉尼,《细菌学杂志》173:6783 - 6789,1991)。在本研究中,我们评估了SpvR在下游毒力基因spvABCD转录中的作用。对mRNA合成的分析表明,SpvR在稳定生长期促进下游spvABCD基因的转录。spv区域的转录图谱显示了一种不寻常的操纵子结构,涉及spvA、spvAB、spvABC和spvABCD的信使RNA。通过使用翻译性spv - lacZ融合对转录和基因表达进行定量测量表明,SpvA、SpvB、SpvC和SpvD的产生丰度逐渐降低。引物延伸试验在spvA起始密码子上游70和98bp处鉴定出两个转录起始位点,但在spvB、spvC或spvD上游未鉴定到。缺失包含这两个起始位点的320bp EcoRI - ApaI片段消除了下游spvB和spvC基因的表达。我们的结果确立了SpvR作为细菌生长稳定期下游spvABCD基因正调控因子的核心功能,并表明主要调控机制是通过激活spvA上游的启动子。