Department of Entomology and Plant Pathology, Auburn University, Auburn, AL, USA.
Appl Environ Microbiol. 2012 Mar;78(5):1321-31. doi: 10.1128/AEM.06501-11. Epub 2011 Dec 22.
Xylella fastidiosa is a plant-pathogenic bacterium that forms biofilms inside xylem vessels, a process thought to be influenced by the chemical composition of xylem sap. In this work, the effect of calcium on the production of X. fastidiosa biofilm and movement was analyzed under in vitro conditions. After a dose-response study with 96-well plates using eight metals, the strongest increase of biofilm formation was observed when medium was supplemented with at least 1.0 mM CaCl(2). The removal of Ca by extracellular (EGTA, 1.5 mM) and intracellular [1,2-bis(o-aminophenoxy)ethane-N,N,N',N'-tetraacetic acid acetoxymethyl ester (BAPTA/AM), 75 μM] chelators reduced biofilm formation without compromising planktonic growth. The concentration of Ca influenced the force of adhesion to the substrate, biofilm thickness, cell-to-cell aggregation, and twitching motility, as shown by assays with microfluidic chambers and other assays. The effect of Ca on attachment was lost when cells were treated with tetracycline, suggesting that Ca has a metabolic or regulatory role in cell adhesion. A double mutant (fimA pilO) lacking type I and type IV pili did not improve biofilm formation or attachment when Ca was added to the medium, while single mutants of type I (fimA) or type IV (pilB) pili formed more biofilm under conditions of higher Ca concentrations. The concentration of Ca in the medium did not significantly influence the levels of exopolysaccharide produced. Our findings indicate that the role of Ca in biofilm formation may be related to the initial surface and cell-to-cell attachment and colonization stages of biofilm establishment, which rely on critical functions by fimbrial structures.
速生丛枝菌是一种植物病原细菌,它在木质部导管内形成生物膜,这一过程被认为受到木质部汁液化学成分的影响。在这项工作中,分析了在体外条件下钙对生防丛枝菌生物膜形成和运动的影响。使用 96 孔板进行了 8 种金属的剂量反应研究后,发现当培养基中补充至少 1.0 mM CaCl(2)时,生物膜形成的增加最为明显。通过细胞外(EGTA,1.5 mM)和细胞内[1,2-双(邻氨基苯氧基)乙烷-N,N,N',N'-四乙酸乙酰氧甲酯(BAPTA/AM),75 μM]螯合剂去除 Ca 会减少生物膜形成,但不会影响浮游生长。Ca 的浓度影响对底物的粘附力、生物膜厚度、细胞间聚集和辗转运动,这可以通过微流控室和其他测定来证明。当用四环素处理细胞时,Ca 对附着的影响消失,这表明 Ca 在细胞附着中具有代谢或调节作用。当向培养基中添加 Ca 时,缺乏 I 型和 IV 型菌毛的双突变体(fimA pilO)不能改善生物膜形成或附着,而当培养基中 Ca 浓度较高时,I 型(fimA)或 IV 型(pilB)菌毛的单突变体形成更多的生物膜。培养基中 Ca 的浓度对产生的胞外多糖水平没有显著影响。我们的研究结果表明,Ca 在生物膜形成中的作用可能与生物膜建立的初始表面和细胞间附着和定植阶段有关,这依赖于菌毛结构的关键功能。