Stewart P S
Center for Biofilm Engineering, Montana State University, Bozeman 59717-0398.
Antimicrob Agents Chemother. 1994 May;38(5):1052-8. doi: 10.1128/AAC.38.5.1052.
A computer model of biofilm dynamics was adapted to incorporate the activity of an antimicrobial agent on bacterial biofilm. The model was used to evaluate the plausibility of two mechanisms of biofilm antibiotic resistance by qualitative comparison with data from a well-characterized experimental system (H. Anwar, J. L. Strap, and J. W. Costerton, Antimicrob. Agents Chemother. 36:1208-1214, 1992). The two mechanisms involved either depletion of the antibiotic by reaction with biomass or physiological resistance due to reduced bacterial growth rates in the biofilm. Both mechanisms predicted the experimentally observed resistance of 7-day-old Pseudomonas aeruginosa biofilms compared with that of 2-day-old ones. A version of the model that incorporated growth rate-dependent killing predicted reduced susceptibility of thicker biofilms because oxygen was exhausted within these biofilms, leading to very slow growth in part of the biofilm. A version of the model that incorporated a destructive reaction of the antibiotic with biomass likewise accounted for the relative resistance of thicker biofilms. Resistance in this latter case was due to depletion of the antibiotic in the bulk fluid rather than development of a gradient in the antibiotic concentration within the biofilm. The modeling results predicted differences between the two cases, such as in the survival profiles within the biofilm, that could permit these resistance mechanisms to be experimentally distinguished.
一种生物膜动力学的计算机模型经过调整,纳入了抗菌剂对细菌生物膜的作用。该模型通过与一个特征明确的实验系统(H. 安瓦尔、J. L. 斯特拉普和J. W. 科斯特顿,《抗菌剂与化疗》36:1208 - 1214, 1992)的数据进行定性比较,用于评估生物膜抗生素抗性的两种机制的合理性。这两种机制要么是抗生素与生物量反应导致其消耗,要么是由于生物膜中细菌生长速率降低而产生生理抗性。两种机制都预测了7日龄铜绿假单胞菌生物膜与2日龄生物膜相比实验观察到的抗性。纳入生长速率依赖性杀灭作用的模型版本预测,较厚的生物膜敏感性降低,因为这些生物膜内氧气耗尽,导致生物膜部分区域生长非常缓慢。纳入抗生素与生物量发生破坏反应的模型版本同样解释了较厚生物膜的相对抗性。在后一种情况下,抗性是由于本体流体中抗生素的消耗,而不是生物膜内抗生素浓度梯度的形成。建模结果预测了这两种情况之间的差异,例如生物膜内的存活曲线,这可以使这些抗性机制在实验中得以区分。