Stibitz S, Weiss A A, Falkow S
Department of Medical Microbiology, Stanford University, California 94305.
J Bacteriol. 1988 Jul;170(7):2904-13. doi: 10.1128/jb.170.7.2904-2913.1988.
The vir locus of Bordetella pertussis apparently encodes a trans-acting positive regulator that is required for the coordinate expression of genes associated with virulence: pertussis toxin, filamentous hemagglutinin (FHA), hemolysin, and adenylate cyclase toxin. DNA clones of vir and of genes required for the synthesis of some of the factors under vir control were obtained with DNA probes from the chromosomal DNA surrounding sites of Tn5 insertion mutations that inactivated those genes. Two vir clones were found which also contained genes required for the proper expression of FHA in B. pertussis. The plasmids which contained both the fha and vir genes expressed immunologically reactive FHA in Escherichia coli, as detected by colony blots, whereas plasmids which contained only fha or vir were negative in this assay. The regulation of FHA production in E. coli, as in B. pertussis, was temperature dependent and inhibited by high concentrations of either magnesium ions or nicotinic acid, indicating that the sequences cloned in E. coli contained the information required to preserve the physiological responses seen in B. pertussis. Further characterization of the vir-fha clones by Tn5 mutagenesis in E. coli and by the return of cloned sequences to B. pertussis in trans and to the B. pertussis chromosome led to the localization of the vir locus, the structural gene for FHA, and genes that are possibly required for the synthesis and export of FHA.
百日咳博德特氏菌的vir位点显然编码一种反式作用的正调控因子,该因子是与毒力相关基因(百日咳毒素、丝状血凝素(FHA)、溶血素和腺苷酸环化酶毒素)协同表达所必需的。利用来自Tn5插入突变失活这些基因的位点周围染色体DNA的DNA探针,获得了vir以及vir控制下某些因子合成所需基因的DNA克隆。发现了两个vir克隆,它们还包含百日咳博德特氏菌中FHA正确表达所需的基因。通过菌落印迹检测,含有fha和vir基因的质粒在大肠杆菌中表达免疫反应性FHA,而仅含有fha或vir的质粒在该检测中呈阴性。与百日咳博德特氏菌一样,大肠杆菌中FHA产生的调控也依赖温度,并受到高浓度镁离子或烟酸的抑制,这表明在大肠杆菌中克隆的序列包含了维持百日咳博德特氏菌中所见生理反应所需的信息。通过在大肠杆菌中进行Tn5诱变以及将克隆序列反式导入百日咳博德特氏菌和导入百日咳博德特氏菌染色体,对vir - fha克隆进行进一步表征,从而确定了vir位点、FHA的结构基因以及可能是FHA合成和输出所需的基因的定位。