Rosan B, Appelbaum B, Campbell L K, Knox K W, Wicken A J
Infect Immun. 1982 Jan;35(1):64-70. doi: 10.1128/iai.35.1.64-70.1982.
Streptococcus sanguis is a major component of early dental plaque. The ability of S. sanguis to adhere to salivary pellicle appears to involve specific bacterial surface receptors. The nature of these receptors is still not known; however, the component molecules may be subject to environmental control as has been shown for teichoic acids and certain proteins. To study these environmental effects, a chemostat was employed to vary the growth conditions of Streptococcus sanguis strain G9B. This strain has been used extensively to study the adhesion of [(3)H]thymidine-labeled batch-grown cells to saliva-coated hydroxyapatite beads. The effects of dilution rate, pH, and carbon source on adhesion were studied with a competition assay in which the labeled batch cells were used as a reference standard. In this assay, cells from the chemostat were harvested and compared for their ability to inhibit adhesion of labeled cells relative to unlabeled control batch-grown cells. Subsequent studies used chemostat grown cells labeled with [(3)H]thymidine as a reference standard so that results were internally controlled and reflected only the particular alteration in environment which was studied. These results indicated that when glucose was used as a growth-limiting substrate, cells grown at relatively high dilution rates (D = 0.5 h(-1); mean generation time = 1.4 h) behaved similarly to batch-grown cells and appeared to compete for the same binding sites. Cells grown at D = 0.1 h(-1) (mean generation time = 7 h) no longer competed with either batch-grown cells or chemostat cells grown at D = 0.5 h(-1). Moreover, adsorption isotherms of such slow-growing cells (D = 0.1 h(-1)) suggested that binding was no longer specific. When fructose was used as the growth-limiting carbohydrate, cells grown at D = 0.1 h(-1) did not show this loss of specificity and competed nearly as well as control batch-grown glucose cells. However, the effect of pH appeared to be independent of carbohydrate source, because cells grown in either glucose or fructose at pH 5.5 at D = 0.1 h(-1) lost the ability to compete with reference batch or chemostat cells grown at D = 0.5 h(-1). This effect was very sharp, since cells grown in the pH range from 6 to 7.5 at D = 0.5 h(-1) competed nearly as well as control cells. A similar effect of pH was found for batch cultures grown with excess glucose. These studies reinforce the idea that the environment can profoundly affect the bacterial surface and consequently the ability of the organism to adhere, a property which appears to be a primary event in some infectious diseases and in dental plaque formation.
血链球菌是早期牙菌斑的主要成分。血链球菌黏附于唾液薄膜的能力似乎涉及特定的细菌表面受体。这些受体的性质尚不清楚;然而,其组成分子可能受环境控制,就像磷壁酸和某些蛋白质那样。为了研究这些环境影响,采用恒化器来改变血链球菌G9B菌株的生长条件。该菌株已被广泛用于研究[³H]胸腺嘧啶核苷标记的分批培养细胞对唾液包被的羟基磷灰石珠的黏附。通过竞争试验研究稀释率、pH值和碳源对黏附的影响,其中将标记的分批培养细胞用作参考标准。在该试验中,收获恒化器中的细胞,并比较它们相对于未标记的对照分批培养细胞抑制标记细胞黏附的能力。后续研究使用用[³H]胸腺嘧啶核苷标记的恒化器培养细胞作为参考标准,以便结果得到内部对照,并且仅反映所研究的特定环境变化。这些结果表明,当葡萄糖用作生长限制底物时,在相对较高稀释率(D = 0.5 h⁻¹;平均世代时间 = 1.4 h)下生长的细胞表现得与分批培养细胞相似,并且似乎竞争相同的结合位点。在D = 0.1 h⁻¹(平均世代时间 = 7 h)下生长的细胞不再与分批培养细胞或在D = 0.5 h⁻¹下生长的恒化器细胞竞争。此外,这种缓慢生长细胞(D = 0.1 h⁻¹)的吸附等温线表明结合不再具有特异性。当果糖用作生长限制碳水化合物时,在D = 0.1 h⁻¹下生长的细胞没有表现出这种特异性丧失,并且竞争能力几乎与对照分批培养的葡萄糖细胞相同。然而,pH值的影响似乎与碳水化合物来源无关,因为在pH 5.5、D = 0.1 h⁻¹下在葡萄糖或果糖中生长的细胞失去了与在D = 0.5 h⁻¹下生长的参考分批或恒化器细胞竞争的能力。这种影响非常明显,因为在D = 0.5 h⁻¹下在pH 6至7.5范围内生长的细胞竞争能力几乎与对照细胞相同。在用过量葡萄糖培养的分批培养物中也发现了类似的pH值影响。这些研究强化了这样一种观点,即环境可以深刻影响细菌表面,从而影响生物体的黏附能力,这种特性似乎是某些传染病和牙菌斑形成中的一个主要事件。