Parker Dane, Kennan Ruth M, Myers Garry S, Paulsen Ian T, Songer J Glenn, Rood Julian I
Australian Research Council Centre of Excellence for Structrral and Functional Microbial Genomics and Victorian Bioinformatics Consortium, Department of Microbiology, Monash University, Victoria 3800, Australia.
J Bacteriol. 2006 Jul;188(13):4801-11. doi: 10.1128/JB.00255-06.
Type IV fimbriae are expressed by several bacterial pathogens and are essential for virulence in Dichelobacter nodosus, which causes ovine footrot. We have identified a two-component signal transduction system (PilR/S) and an alternative sigma factor (sigma 54) that were shown by insertional inactivation to be required for the regulation of fimbrial biogenesis in D. nodosus. Western blots showed that in both pilR and rpoN mutants, fimbrial subunit production was significantly reduced by a process that was shown to occur at a PilR- and sigma 54-dependent promoter. The mutants lacked surface fimbriae, which were shown to be required for the adherence of D. nodosus cells to tissue culture monolayers. The reduction in fimbrial subunit production in these mutants also resulted in a concomitant loss of the ability to secrete extracellular proteases. A maltose binding protein-PilR fusion protein was purified and was shown to bind specifically to a region located 234 to 594 bp upstream of the fimA transcriptional start point. To determine additional targets of PilR and sigma 54, genome-wide transcriptional profiling was performed using a whole-genome oligonucleotide microarray. The results indicated that PilR and sigma 54 regulated genes other than fimA; these genes appear to encode surface-exposed proteins whose role in virulence is unknown. In conclusion, this study represents a significant advancement in our understanding of how the ability of D. nodosus to cause ovine footrot is regulated, as we have shown that the biogenesis of type IV fimbriae in D. nodosus is regulated by a sigma 54-dependent PilR/S system that also indirectly controls protease secretion.
IV型菌毛由多种细菌病原体表达,对于引起羊腐蹄病的结节拟杆菌的毒力至关重要。我们鉴定出了一个双组分信号转导系统(PilR/S)和一个替代σ因子(σ54),通过插入失活表明它们是结节拟杆菌菌毛生物合成调控所必需的。蛋白质免疫印迹显示,在pilR和rpoN突变体中,菌毛亚基产量通过一个在PilR和σ54依赖性启动子处发生的过程而显著降低。这些突变体缺乏表面菌毛,而表面菌毛被证明是结节拟杆菌细胞粘附于组织培养单层所必需的。这些突变体中菌毛亚基产量的降低也导致了分泌细胞外蛋白酶能力的相应丧失。纯化了一种麦芽糖结合蛋白-PilR融合蛋白,结果显示它能特异性结合位于fimA转录起始点上游234至594 bp的区域。为了确定PilR和σ54 的其他靶点,使用全基因组寡核苷酸微阵列进行了全基因组转录谱分析。结果表明PilR和σ54调控fimA以外 的基因;这些基因似乎编码表面暴露蛋白,但它们在毒力中的作用尚不清楚。总之,本研究在我们对结节拟杆菌引起羊腐蹄病能力的调控理解方面取得了重大进展,因为我们已经表明结节拟杆菌中IV型菌毛 的生物合成受一个σ54依赖性PilR/S系统调控,该系统还间接控制蛋白酶分泌。