Ciacci-Woolwine F, Blomfield I C, Richardson S H, Mizel S B
Department of Microbiology and Immunology, Wake Forest University Medical Center, Winston-Salem, North Carolina 27157, USA.
Infect Immun. 1998 Mar;66(3):1127-34. doi: 10.1128/IAI.66.3.1127-1134.1998.
During infection of the gastrointestinal tract, salmonellae induce cytokine production and inflammatory responses which are believed to mediate tissue damage in the host. In a previous study, we reported that salmonellae possess the ability to stimulate tumor necrosis factor alpha (TNF-alpha) accumulation in primary human monocytes, as well as in the human promonocytic cell line U38. In this model system, cytokine upregulation is not due to lipopolysaccharide but is mediated by a released protein. In the present study, TnphoA transposon mutagenesis was used to identify the TNF-alpha-inducing factor. A mutant Salmonella strain which lacks the ability to induce TNF-alpha was isolated from a TnphoA library. Genetic analysis of this mutant demonstrated that the hns gene has been interrupted by transposon insertion. The hns gene product is a DNA-binding protein that regulates the expression of a variety of unrelated genes in salmonellae. One of the known targets of histone-like protein H1 is flhDC, the master operon which is absolutely required for flagellar expression. Analysis of other nonflagellated mutant Salmonella strains revealed a correlation between the ability to induce TNF-alpha and the expression of the phase 1 filament subunit protein FliC. Complementation experiments demonstrated that FliC is sufficient to restore the ability of nonflagellated mutant Salmonella strains to upregulate TNF-alpha, whereas the phase 2 protein FljB appears to complement to a lesser extent. In addition, Salmonella FliC can confer the TNF-alpha-inducing phenotype on Escherichia coli, which otherwise lacks the activity. Furthermore, assembly of FliC into complete flagellar structures may not be required for induction of TNF-alpha.
在胃肠道感染过程中,沙门氏菌会诱导细胞因子的产生和炎症反应,据信这些反应会介导宿主组织损伤。在先前的一项研究中,我们报道沙门氏菌具有刺激原代人单核细胞以及人早幼单核细胞系U38中肿瘤坏死因子α(TNF-α)积累的能力。在这个模型系统中,细胞因子的上调并非由于脂多糖,而是由一种释放的蛋白质介导。在本研究中,使用TnphoA转座子诱变来鉴定TNF-α诱导因子。从TnphoA文库中分离出一株缺乏诱导TNF-α能力的突变沙门氏菌菌株。对该突变体的遗传分析表明,hns基因已被转座子插入打断。hns基因产物是一种DNA结合蛋白,可调节沙门氏菌中多种不相关基因的表达。组蛋白样蛋白H1的已知靶标之一是flhDC,它是鞭毛表达绝对必需的主操纵子。对其他无鞭毛突变沙门氏菌菌株的分析揭示了诱导TNF-α的能力与1期鞭毛亚基蛋白FliC的表达之间的相关性。互补实验表明,FliC足以恢复无鞭毛突变沙门氏菌菌株上调TNF-α的能力,而2期蛋白FljB的互补程度似乎较小。此外,沙门氏菌FliC可赋予大肠杆菌TNF-α诱导表型,否则大肠杆菌缺乏该活性。此外,TNF-α的诱导可能不需要FliC组装成完整的鞭毛结构。