Section of Molecular Genetics and Microbiology and Institute of Cellular and Molecular Biology, University of Texas at Austin, Austin, Texas, USA.
J Bacteriol. 2013 Mar;195(5):909-18. doi: 10.1128/JB.02063-12. Epub 2012 Dec 21.
Movement over an agar surface via swarming motility is subject to formidable challenges not encountered during swimming. Bacteria display a great deal of flexibility in coping with these challenges, which include attracting water to the surface, overcoming frictional forces, and reducing surface tension. Bacteria that swarm on "hard" agar surfaces (robust swarmers) display a hyperflagellated and hyperelongated morphology. Bacteria requiring a "softer" agar surface (temperate swarmers) do not exhibit such a dramatic morphology. For polarly flagellated robust swarmers, there is good evidence that restriction of flagellar rotation somehow signals the induction of a large number of lateral flagella, but this scenario is apparently not relevant to temperate swarmers. Swarming bacteria can be further subdivided by their requirement for multiple stators (Mot proteins) or a stator-associated protein (FliL), secretion of essential polysaccharides, cell density-dependent gene regulation including surfactant synthesis, a functional chemotaxis signaling pathway, appropriate cyclic (c)-di-GMP levels, induction of virulence determinants, and various nutritional requirements such as iron limitation or nitrate availability. Swarming strategies are as diverse as the bacteria that utilize them. The strength of these numerous designs stems from the vantage point they offer for understanding mechanisms for effective colonization of surface niches, acquisition of pathogenic potential, and identification of environmental signals that regulate swarming. The signature swirling and streaming motion within a swarm is an interesting phenomenon in and of itself, an emergent behavior with properties similar to flocking behavior in diverse systems, including birds and fish, providing a convenient new avenue for modeling such behavior.
在琼脂表面通过群体运动进行的运动面临着游泳时不会遇到的巨大挑战。细菌在应对这些挑战方面表现出很大的灵活性,包括吸引水到表面、克服摩擦力和降低表面张力。在“硬”琼脂表面上进行群体运动的细菌(强健的群体运动细菌)表现出高度鞭毛化和超伸长的形态。需要更“软”琼脂表面的细菌(温和的群体运动细菌)则不会表现出如此显著的形态。对于极性鞭毛的强健群体运动细菌,有充分的证据表明,鞭毛旋转的限制以某种方式信号诱导大量侧鞭毛的产生,但这种情况显然与温和的群体运动细菌无关。群体运动细菌可以根据其对多个定子(Mot 蛋白)或定子相关蛋白(FliL)、必需多糖分泌、细胞密度依赖性基因调控(包括表面活性剂合成)、功能化的化学趋化信号通路、适当的环(c)-二鸟苷酸(c-di-GMP)水平、毒力决定因素的诱导以及各种营养需求(如铁限制或硝酸盐可用性)的要求进一步细分。群体运动策略与利用它们的细菌一样多样化。这些众多设计的优势在于它们为理解有效定殖表面生态位、获得致病性潜力以及识别调节群体运动的环境信号的机制提供了有利的视角。群体内部的漩涡和流动物体本身就是一个有趣的现象,是一种具有类似不同系统中集群行为(包括鸟类和鱼类)特性的涌现行为,为模拟这种行为提供了一个方便的新途径。