Belas R, Erskine D, Flaherty D
Center of Marine Biotechnology, University of Maryland, Baltimore 21202.
J Bacteriol. 1991 Oct;173(19):6279-88. doi: 10.1128/jb.173.19.6279-6288.1991.
Proteus mirabilis is a dimorphic bacterium which exists in liquid cultures as a 1.5- to 2.0-microns motile swimmer cell possessing 6 to 10 peritrichous flagella. When swimmer cells are placed on a surface, they differentiate by a combination of events that ultimately produce a swarmer cell. Unlike the swimmer cell, the polyploid swarmer cell is 60 to 80 microns long and possesses hundreds to thousands of surface-induced flagella. These features, combined with multicellular behavior, allow the swarmer cells to move over a surface in a process called swarming. Transposon Tn5 was used to produce P. mirabilis mutants defective in wild-type swarming motility. Two general classes of mutants were found to be defective in swarming. The first class was composed of null mutants that were completely devoid of swarming motility. The majority of nonswarming mutations were the result of defects in the synthesis of flagella or in the ability to rotate the flagella. The remaining nonswarming mutants produced flagella but were defective in surface-induced elongation. Strains in the second general class of mutants, which made up more than 65% of all defects in swarming were motile but were defective in the control and coordination of multicellular swarming. Analysis of consolidation zones produced by such crippled mutants suggested that this pleiotropic phenotype was caused by a defect in the regulation of multicellular behavior. A possible mechanism controlling the cyclic process of differentiation and dediferentiation involved in the swarming behavior of P. mirabilis is discussed.
奇异变形杆菌是一种双态细菌,在液体培养物中以1.5至2.0微米的具运动性的游动细胞形式存在,有6至10根周生鞭毛。当游动细胞置于表面时,它们会通过一系列最终产生群体游动细胞的事件而发生分化。与游动细胞不同,多倍体群体游动细胞长60至80微米,拥有数百至数千根表面诱导产生的鞭毛。这些特征与多细胞行为相结合,使群体游动细胞能够在一个称为群体游动的过程中在表面移动。转座子Tn5被用于产生在野生型群体游动运动方面有缺陷的奇异变形杆菌突变体。发现有两类一般的突变体在群体游动方面有缺陷。第一类由完全没有群体游动运动能力的无效突变体组成。大多数不发生群体游动的突变是由于鞭毛合成缺陷或鞭毛旋转能力缺陷所致。其余不发生群体游动的突变体产生鞭毛,但在表面诱导伸长方面有缺陷。第二类一般的突变体中的菌株占群体游动所有缺陷的65%以上,它们具有运动能力,但在多细胞群体游动的控制和协调方面有缺陷。对这类有缺陷的突变体产生的合并区域的分析表明,这种多效性表型是由多细胞行为调节缺陷引起的。本文讨论了一种可能控制奇异变形杆菌群体游动行为中涉及的分化和去分化循环过程的机制。