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Genetic analysis of a region of the Bordetella pertussis chromosome encoding filamentous hemagglutinin and the pleiotropic regulatory locus vir.

机译:百日咳博德特氏菌染色体区域编码丝状血凝素和多效性调节位点vir的遗传分析。

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摘要

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.
机译:百日咳博德特氏菌的病毒基因座显然编码一个反式作用的正调节剂,它是与毒力相关的基因的协调表达所必需的:百日咳毒素,丝状血凝素(FHA),溶血素和腺苷酸环化酶毒素。用DNA探针从灭活那些基因的Tn5插入突变的染色体DNA周围位点获得vir和一些在vir控制下合成某些因子所需基因的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。如通过菌落印迹所检测,同时包含fha和vir基因的质粒在大肠杆菌中表达免疫反应性FHA,而在此测定中仅包含fha或vir的质粒是阴性的。如百日咳博德特氏菌一样,大肠杆菌中FHA产生的调节是温度依赖性的,并受到高浓度的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保持生理反应所需的信息。见于百日咳博德特氏菌。通过在大肠杆菌中进行Tn5诱变并通过将克隆的序列反过来转化为百日咳博德特氏菌和百日咳博德特氏菌染色体来进一步表征vir-fha克隆,从而导致了病毒基因座(FHA的结构基因)的定位,以及合成和输出FHA可能需要的基因。

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