Center of Marine Biotechnology, University of Maryland Biotechnology Institute, University of Maryland System, 600 East Lombard Street, Baltimore, Maryland 21202.
Appl Environ Microbiol. 1992 Sep;58(9):2954-9. doi: 10.1128/aem.58.9.2954-2959.1992.
Microcosm studies were performed to evaluate the effect of solid surfaces, bacterial adhesive ability, and inoculum size on colonization success and persistence of Pseudomonas fluorescens and Xanthomonas maltophilia, each with a Tn5 insertion that conferred resistance to kanamycin and streptomycin. Two types of microcosms were used: (i) a simple system that was colonized by Aeromonas hydrophila and a coryneform and (ii) a complex system produced from lake water enrichment cultures. Simple microcosms contained 100 ml of peptone- and yeast extract-supplemented artificial lake water or 60 ml of peptone- and yeast extract-supplemented artificial lake water with 70 g of 3-mm glass beads. Complex microcosms contained 100 ml of lake water with no nutrient additions or 100 ml of lake water with 70 g of glass beads. The microcosms were incubated for 35 days at 20 degrees C. In lake water enrichment microcosms, the presence of beads increased the abilities of P. fluorescens or X. maltophilia to colonize, but their numbers decreased with time in microcosms both with and without beads. The adhesiveness of the bacteria, measured in an in vitro assay, did not relate to colonization success. In simple microcosms, the inoculum size (10, 10, or 10) of P. fluorescens did not influence colonization success. However, in complex microcosms, an inoculum of 10 cells was insufficient to ensure colonization by P. fluorescens, while 10 cells resulted in colonization of liquid and beads. Simple microcosm studies, utilizing only a few species, were poor models for complex natural systems. In complex enrichment systems, colonization of surfaces resulted in higher numbers of organisms but did not noticeably promote persistence. Adhesiveness of a particular organism may be a relatively minor factor influencing its ability to colonize solid surfaces in complex natural environments.
微宇宙研究用于评估固体表面、细菌粘附能力和接种量对荧光假单胞菌和嗜麦芽寡养单胞菌定殖成功和持续存在的影响,这两种菌都带有 Tn5 插入,赋予了对卡那霉素和链霉素的抗性。使用了两种类型的微宇宙:(i)一种简单的系统,由嗜水气单胞菌和棒杆菌组成;(ii)一种从湖水富集培养物中产生的复杂系统。简单微宇宙包含 100 ml 含蛋白胨和酵母提取物的人工湖水或 60 ml 含蛋白胨和酵母提取物的人工湖水,其中含有 70 g 3-mm 玻璃珠。复杂微宇宙包含 100 ml 无营养添加的湖水或 100 ml 含玻璃珠的湖水。微宇宙在 20°C 下孵育 35 天。在湖水富集微宇宙中,珠子的存在增加了荧光假单胞菌或嗜麦芽寡养单胞菌的定殖能力,但在有无珠子的微宇宙中,它们的数量随着时间的推移而减少。在体外测定中,细菌的粘附性与其定殖成功无关。在简单的微宇宙中,荧光假单胞菌的接种量(10、10 或 10)不会影响其定殖成功。然而,在复杂的微宇宙中,10 个细胞的接种量不足以确保荧光假单胞菌的定殖,而 10 个细胞则导致液体和珠子的定殖。简单的微宇宙研究,仅利用少数几个物种,是复杂自然系统的不良模型。在复杂的富集系统中,表面的定殖导致了更多的生物体,但并没有明显促进其持续存在。特定生物体的粘附性可能是影响其在复杂自然环境中定殖固体表面能力的一个相对次要的因素。