McCarter L L, Wright M E
Department of Bacteriology, University of Wisconsin, Madison 53706.
J Bacteriol. 1993 Jun;175(11):3361-71. doi: 10.1128/jb.175.11.3361-3371.1993.
Vibrio parahaemolyticus possesses two distinct motility systems, the polar system used for swimming in liquid environments and the lateral system used for swarming over surfaces. Growth on surfaces induces swarmer cell differentiation and expression of the lateral motility system. Mutants, created by transposon mutagenesis of a clone expressing lateral flagellin and gene disruption in V. parahaemolyticus, were unable to swarm and failed to make lateral flagellin; therefore, unlike the case for the polar system, there is one gene (lafA) encoding lateral flagellin. In addition to lafA, other genes required for swarming but not for swimming were identified by gene replacement mutagenesis. The nucleotide sequence of the clone determined open reading frames (ORFs) and deduced amino acid sequences showed similarities to flagellar components of other bacteria: flagellin, hook-associated protein (HAP2), motor components, and flagellar sigma factor (sigma 28). Many sigma 28 factors have been shown to recognize cognate promoters; however, expression of lafA in Escherichia coli required LafS, and E. coli sigma 28 did not substitute. Also, there were no sequences preceding genes encoding flagellin or HAP2 resembling the sigma 28 consensus promoter. The product of the sigma-like gene seems to be a unique member of the sigma 28 cluster. It appears the result of requiring expression for immunodetection of flagellin clones was that the sigma locus was fortuitously cloned, since the sigma and lafA loci were not contiguous in the chromosome. This work initiates identification and placement of genes in a scheme of control for swarmer cell differentiation; three levels have been identified in the transcriptional hierarchy.
副溶血性弧菌拥有两种不同的运动系统,即用于在液体环境中游泳的极生系统和用于在表面群体游动的侧生系统。在表面生长会诱导群体游动细胞分化和侧生运动系统的表达。通过对表达侧生鞭毛蛋白的克隆进行转座子诱变以及对副溶血性弧菌进行基因破坏而产生的突变体,无法进行群体游动且不能产生侧生鞭毛蛋白;因此,与极生系统不同,只有一个基因(lafA)编码侧生鞭毛蛋白。除了lafA之外,通过基因置换诱变还鉴定出了群体游动而非游泳所必需的其他基因。所确定的克隆的核苷酸序列中的开放阅读框(ORF)以及推导的氨基酸序列与其他细菌的鞭毛成分具有相似性:鞭毛蛋白、钩相关蛋白(HAP2)、运动成分以及鞭毛σ因子(σ28)。许多σ28因子已被证明能识别同源启动子;然而,lafA在大肠杆菌中的表达需要LafS,并且大肠杆菌的σ28不能替代。此外,在编码鞭毛蛋白或HAP2的基因之前没有类似于σ28共有启动子的序列。类σ基因的产物似乎是σ28簇中的一个独特成员。似乎由于需要表达以对鞭毛蛋白克隆进行免疫检测,结果偶然克隆到了σ基因座,因为在染色体中σ和lafA基因座并不相邻。这项工作开启了在群体游动细胞分化控制方案中对基因的鉴定和定位;在转录层次结构中已确定了三个水平。