Schwartz Kelly, Stephenson Rachel, Hernandez Margarita, Jambang Nicolays, Boles Blaise R
Molecular, Cellular, and Developmental Biology, University of Michigan, USA.
J Vis Exp. 2010 Dec 27(46):2470. doi: 10.3791/2470.
Most microbes in nature are thought to exist as surface-associated communities in biofilms.(1) Bacterial biofilms are encased within a matrix and attached to a surface.(2) Biofilm formation and development are commonly studied in the laboratory using batch systems such as microtiter plates or flow systems, such as flow-cells. These methodologies are useful for screening mutant and chemical libraries (microtiter plates)(3) or growing biofilms for visualization (flow cells)(4). Here we present detailed protocols for growing Staphylococcus aureus in two additional types of flow system biofilms: the drip flow biofilm reactor and the rotating disk biofilm reactor. Drip flow biofilm reactors are designed for the study of biofilms grown under low shear conditions.(5) The drip flow reactor consists of four parallel test channels, each capable of holding one standard glass microscope slide sized coupon, or a length of catheter or stint. The drip flow reactor is ideal for microsensor monitoring, general biofilm studies, biofilm cryosectioning samples, high biomass production, medical material evaluations, and indwelling medical device testing.(6,7,8,9) The rotating disk reactor consists of a teflon disk containing recesses for removable coupons.(10) The removable coupons can by made from any machinable material. The bottom of the rotating disk contains a bar magnet to allow disk rotation to create liquid surface shear across surface-flush coupons. The entire disk containing 18 coupons is placed in a 1000 mL glass side-arm reactor vessel. A liquid growth media is circulated through the vessel while the disk is rotated by a magnetic stirrer. The coupons are removed from the reactor vessel and then scraped to collect the biofilm sample for further study or microscopy imaging. Rotating disc reactors are designed for laboratory evaluations of biocide efficacy, biofilm removal, and performance of anti-fouling materials.(9,11,12,13).
自然界中的大多数微生物被认为是以生物膜的形式存在于与表面相关的群落中。(1)细菌生物膜被包裹在基质中并附着于表面。(2)生物膜的形成和发展通常在实验室中使用批量系统(如微量滴定板)或流动系统(如流动池)进行研究。这些方法对于筛选突变体和化学文库(微量滴定板)(3)或培养生物膜以进行可视化(流动池)(4)很有用。在这里,我们展示了在另外两种类型的流动系统生物膜中培养金黄色葡萄球菌的详细方案:滴流生物膜反应器和旋转盘生物膜反应器。滴流生物膜反应器设计用于研究在低剪切条件下生长的生物膜。(5)滴流反应器由四个平行的测试通道组成,每个通道能够容纳一张标准玻璃显微镜载玻片大小的试样片,或一段导管或支架。滴流反应器非常适合微传感器监测、一般生物膜研究、生物膜冷冻切片样本、高生物量生产、医疗材料评估以及植入式医疗器械测试。(6,7,8,9)旋转盘反应器由一个含有用于可拆卸试样片凹槽的聚四氟乙烯盘组成。(10)可拆卸试样片可以由任何可加工材料制成。旋转盘的底部包含一个条形磁铁,以允许盘旋转,从而在与表面齐平的试样片上产生液体表面剪切力。将包含18个试样片的整个盘放置在一个1000 mL的玻璃侧臂反应器容器中。当盘由磁力搅拌器旋转时,液体生长培养基在容器中循环。从反应器容器中取出试样片,然后刮擦以收集生物膜样本用于进一步研究或显微镜成像。旋转盘反应器设计用于实验室评估杀菌剂功效、生物膜去除以及防污材料的性能。(9,11,12,13)