Vilain Sébastien, Pretorius Jakobus M, Theron Jacques, Brözel Volker S
Department of Biology and Microbiology, South Dakota State University, Brookings, SD 57007, USA.
Appl Environ Microbiol. 2009 May;75(9):2861-8. doi: 10.1128/AEM.01317-08. Epub 2009 Feb 27.
The soil saprophyte Bacillus cereus forms biofilms at solid-liquid interfaces. The composition of the extracellular polymeric matrix is not known, but biofilms of other bacteria are encased in polysaccharides, protein, and also extracellular DNA (eDNA). A Tn917 screen for strains impaired in biofilm formation at a solid-liquid interface yielded several mutants. Three mutants deficient in the purine biosynthesis genes purA, purC, and purL were biofilm impaired, but they grew planktonically like the wild type in Luria-Bertani broth. Biofilm populations had higher purA, purC, and purL transcript ratios than planktonic cultures, as measured by real-time PCR. Laser scanning confocal microscopy (LSCM) of BacLight-stained samples indicated that there were nucleic acids in the cell-associated matrix. This eDNA could be mobilized off the biofilm into an agarose gel matrix through electrophoresis, and it was a substrate for DNase. Glass surfaces exposed to exponentially growing populations acquired a DNA-containing conditioning film, as indicated by LSCM. Planktonic exponential-phase cells released DNA into an agarose gel matrix through electrophoresis, while stationary-phase populations did not do this. DNase treatment of planktonic exponential-phase populations rendered cells more susceptible than control populations to the DNA-interacting antibiotic actinomycin D. Exponential-phase purA cells did not contain detectable eDNA, nor did they convey a DNA-containing conditioning film to the glass surface. These results indicate that exponential-phase cells of B. cereus ATCC 14579 are decorated with eDNA and that biofilm formation requires DNA as part of the extracellular polymeric matrix.
土壤腐生菌蜡样芽孢杆菌可在固液界面形成生物膜。细胞外聚合物基质的组成尚不清楚,但其他细菌的生物膜被包裹在多糖、蛋白质以及细胞外DNA(eDNA)中。通过Tn917筛选在固液界面生物膜形成受损的菌株,得到了几个突变体。三个嘌呤生物合成基因purA、purC和purL缺陷的突变体生物膜形成受损,但它们在Luria-Bertani肉汤中浮游生长时与野生型相似。通过实时PCR测量,生物膜群体中purA、purC和purL的转录本比率高于浮游培养物。对用BacLight染色的样品进行激光扫描共聚焦显微镜(LSCM)观察表明,细胞相关基质中存在核酸。这种eDNA可通过电泳从生物膜转移到琼脂糖凝胶基质中,并且它是DNase的作用底物。LSCM显示,暴露于指数生长期群体的玻璃表面获得了一层含DNA的调理膜。浮游指数期细胞通过电泳将DNA释放到琼脂糖凝胶基质中,而稳定期群体则不会。用DNase处理浮游指数期群体,使细胞比对照群体对与DNA相互作用的抗生素放线菌素D更敏感。指数期purA细胞不含可检测到的eDNA,也不会在玻璃表面形成含DNA的调理膜。这些结果表明,蜡样芽孢杆菌ATCC 14579的指数期细胞表面有eDNA,并且生物膜形成需要DNA作为细胞外聚合物基质的一部分。