Tolker-Nielsen T, Brinch U C, Ragas P C, Andersen J B, Jacobsen C S, Molin S
Molecular Microbial Ecology Group, Department of Microbiology, The Technical University of Denmark, DK-2800 Lyngby, Denmark.
J Bacteriol. 2000 Nov;182(22):6482-9. doi: 10.1128/JB.182.22.6482-6489.2000.
Pseudomonas sp. strain B13 and Pseudomonas putida OUS82 were genetically tagged with the green fluorescent protein and the Discosoma sp. red fluorescent protein, and the development and dynamics occurring in flow chamber-grown two-colored monospecies or mixed-species biofilms were investigated by the use of confocal scanning laser microscopy. Separate red or green fluorescent microcolonies were formed initially, suggesting that the initial small microcolonies were formed simply by growth of substratum attached cells and not by cell aggregation. Red fluorescent microcolonies containing a few green fluorescent cells and green fluorescent microcolonies containing a few red fluorescent cells were frequently observed in both monospecies and two-species biofilms, suggesting that the bacteria moved between the microcolonies. Rapid movement of P. putida OUS82 bacteria inside microcolonies was observed before a transition from compact microcolonies to loose irregularly shaped protruding structures occurred. Experiments involving a nonflagellated P. putida OUS82 mutant suggested that the movements between and inside microcolonies were flagellum driven. The results are discussed in relation to the prevailing hypothesis that biofilm bacteria are in a physiological state different from planktonic bacteria.
将荧光假单胞菌B13菌株和恶臭假单胞菌OUS82分别用绿色荧光蛋白和盘基网柄菌红色荧光蛋白进行基因标记,利用共聚焦扫描激光显微镜研究了在流动室中生长的双色单物种或混合物种生物膜中的发育和动态变化。最初形成了单独的红色或绿色荧光微菌落,这表明最初的小微菌落仅仅是由附着在基质上的细胞生长形成的,而不是通过细胞聚集形成的。在单物种和双物种生物膜中都经常观察到含有一些绿色荧光细胞的红色荧光微菌落和含有一些红色荧光细胞的绿色荧光微菌落,这表明细菌在微菌落之间移动。在从紧密的微菌落转变为松散的不规则形状突出结构之前,观察到恶臭假单胞菌OUS82细菌在微菌落内部快速移动。涉及无鞭毛恶臭假单胞菌OUS82突变体的实验表明,微菌落之间和内部的移动是由鞭毛驱动的。结合生物膜细菌处于与浮游细菌不同生理状态这一普遍假设对结果进行了讨论。