Laboratory of Food Microbiology and Hygiene, Department of Food Science and Technology, School of Agriculture, Aristotle University of Thessaloniki, Thessaloniki 54124, Greece.
Int J Food Microbiol. 2012 Nov 15;160(2):171-8. doi: 10.1016/j.ijfoodmicro.2012.10.002. Epub 2012 Oct 7.
The biofilm-forming ability of 60 Salmonella enterica strains was assessed at different pH values (3.8-7.0), NaCl concentrations (0.5-8.0%) and temperatures (4-37°C). A total of 4320 biofilm formation tests (60 strains×12 different environmental conditions×6 replicates) were carried out. Biofilm formation was evaluated in tryptone soy broth after 48h of incubation in polystyrene microtiter plates using crystal violet staining, and its quantification was based on the difference between the optical density measurements of the test and negative control (uninoculated) samples (ΔOD(580nm)). The tested strains formed biofilms under a wide range of environmental conditions, while extensive strain variability was observed with the mean ΔOD(580nm) values ranging from 0 to 2.388 depending on the strain and the condition evaluated. The strain variability of biofilm formation was affected by all three of the environmental parameters tested, and appeared to increase as the environmental conditions became less favorable for the organism. In addition, the increase in the strain variability caused by pH was found to be much greater than that caused by NaCl or temperature. For example, the coefficient of variation (CV=standard deviation/mean∗100) of ΔOD(580nm) among the tested strains at pH 7.0-0.5% NaCl-37°C was 104%, while at pH 3.8-0.5% NaCl-37°C, pH 7.0-8.0% NaCl-37°C and pH 7.0-0.5% NaCl-8°C was 351.5%, 204.1% and 175.6%, respectively. The optimum conditions for biofilm formation, providing the maximum ΔOD(580nm), varied significantly among the tested strains. Among the evaluated conditions, most of the S. enterica strains were clustered as forming their highest amount of biofilm at pH 5.5 (35 strains; 58.3%), at 0.5% NaCl (29 strains; 48.3%) and at 25°C (32 strains; 53.3%). No relationships were observed between the biofilm-forming ability of the strains and their serotype or their growth kinetic behavior as this was evaluated in a previous study. The findings of this study provide useful information in advancing the current understanding of strain variability, as well as in strain selection for the evaluation of the efficacy of disinfection/sanitation procedures against biofilm formation.
评估了 60 株肠炎沙门氏菌在不同 pH 值(3.8-7.0)、NaCl 浓度(0.5-8.0%)和温度(4-37°C)下的生物膜形成能力。共进行了 4320 次生物膜形成测试(60 株×12 种不同环境条件×6 个重复)。在聚苯乙烯微量滴定板中用结晶紫染色孵育 48 小时后,在胰蛋白胨大豆肉汤中评估生物膜形成,并根据测试和阴性对照(未接种)样品之间的吸光度测量值差异(ΔOD(580nm))进行定量。测试菌株在广泛的环境条件下形成生物膜,而根据菌株和评估的条件,平均 ΔOD(580nm)值的范围从 0 到 2.388,表明菌株间存在广泛的变异性。生物膜形成的菌株变异性受到所有三个测试环境参数的影响,并且随着环境条件对生物体变得越来越不利而增加。此外,发现由 pH 引起的菌株变异性增加大于由 NaCl 或温度引起的菌株变异性增加。例如,在 pH 7.0-0.5%NaCl-37°C 下,测试菌株之间的 ΔOD(580nm)的变异系数(CV=标准差/平均值∗100)为 104%,而在 pH 3.8-0.5%NaCl-37°C、pH 7.0-8.0%NaCl-37°C 和 pH 7.0-0.5%NaCl-8°C 时,分别为 351.5%、204.1%和 175.6%。生物膜形成的最佳条件,提供最大的 ΔOD(580nm),在测试菌株之间有很大差异。在所评估的条件中,大多数肠炎沙门氏菌菌株被聚类为在 pH 5.5(35 株;58.3%)、0.5%NaCl(29 株;48.3%)和 25°C(32 株;53.3%)下形成最高量的生物膜。在本研究中,没有观察到菌株的生物膜形成能力与其血清型或之前研究中评估的生长动力学行为之间存在关系。本研究的结果为深入了解菌株变异性以及选择用于评估消毒/卫生程序对生物膜形成的效果的菌株提供了有用的信息。