Friedrich M J, Kinsey N E, Vila J, Kadner R J
Department of Microbiology, School of Medicine, University of Virginia, Charlottesville 22908.
Mol Microbiol. 1993 May;8(3):543-58. doi: 10.1111/j.1365-2958.1993.tb01599.x.
The 90kb plasmid resident in Salmonella typhimurium confers increased virulence in mice by promoting the spread of infection after invasion of the intestinal epithelium. The nucleotide sequence of a 13.9kb segment of this plasmid known to encode an outer membrane protein related in sequence to components of fimbrial biosynthesis in enteric bacteria was determined. This cloned segment between the repB and repC replicon regions programmed expression of abundant surface fimbriae in Escherichia coli and S. typhimurium cells. A 7kb region contained seven open reading frames, the protein products of five of which were related in sequence to regulatory, structural, and assembly proteins of adherence fimbriae/pili, such as the P and K88 pili. These five genes and two adjacent ones which were not markedly related to proteins in the data bases comprise the pef (plasmid-encoded fimbriae) locus. Transposon TnphoA insertions in four genes in the pef locus (pefA, pefC, orf5 and orf6) resulted in active PhoA fusions and blocked or reduced the surface presentation of fimbriae, indicating that the proteins encoded by these four genes are translocated at least across the cytoplasmic membrane and contribute to formation of the fimbrial structure. The differences in genetic organization and protein sequence relatedness from other fimbrial gene clusters suggest that the pef locus might encode a novel type of fimbria. Between the pef and the repB loci, there were five open reading frames, one of which (orf8) gave rise to active PhoA fusions but was not necessary for fimbrial expression. Two of the other proteins were homologous to transcription regulatory proteins and a third was the rck gene, which encodes an outer membrane protein that confers complement resistance to serum-sensitive hosts.
鼠伤寒沙门氏菌中存在的90kb质粒通过促进肠道上皮细胞入侵后感染的传播,增强了小鼠的毒力。确定了该质粒13.9kb片段的核苷酸序列,已知该片段编码一种外膜蛋白,其序列与肠道细菌菌毛生物合成成分相关。该克隆片段位于repB和repC复制子区域之间,可在大肠杆菌和鼠伤寒沙门氏菌细胞中编程表达丰富的表面菌毛。一个7kb的区域包含七个开放阅读框,其中五个的蛋白质产物在序列上与粘附菌毛/菌毛的调节、结构和组装蛋白相关,如P菌毛和K88菌毛。这五个基因以及另外两个与数据库中的蛋白质无明显相关性的相邻基因组成了pef(质粒编码菌毛)位点。转座子TnphoA插入pef位点的四个基因(pefA、pefC、orf5和orf6)中,导致活性PhoA融合,并阻断或减少了菌毛的表面呈现,表明这四个基因编码的蛋白质至少穿过细胞质膜,并有助于菌毛结构的形成。与其他菌毛基因簇在遗传组织和蛋白质序列相关性上的差异表明,pef位点可能编码一种新型菌毛。在pef和repB位点之间,有五个开放阅读框,其中一个(orf8)产生了活性PhoA融合,但对菌毛表达不是必需的。另外两种蛋白质与转录调节蛋白同源,第三种是rck基因,它编码一种外膜蛋白,赋予血清敏感宿主对补体的抗性。