Sissons C H
Department of Pathology, Wellington School of Medicine, University of Otago, New Zealand.
Adv Dent Res. 1997 Apr;11(1):110-26. doi: 10.1177/08959374970110010201.
Difficulties with in vivo studies of natural plaque and its complex, heterogeneous structure have led to development of laboratory biofilm plaque model systems. Technologies for their culture are outlined, and the rationale, strengths, and relative uses of two complementary approaches to microbial models with a focus on plaque biodiversity are analyzed. Construction of synthetic consortia biofilms of major plaque species has established a variety of bacterial interactions important in plaque development. In particular, the 'Marsh' nine-species biofilm consortia systems are powerful quasi steady-state models which can be closely specified, modified, and analyzed. In the second approach, microcosm plaque biofilms are evolved in vitro from the natural oral microflora to the laboratory model most closely related to plaque in vivo. Functionally reproducible microcosm plaques are attainable with a biodiverse microbiota, heterogeneous structure, and pH behavior consistent with those of natural plaque. The resting pH can be controlled by urea supply. Their growth patterns, pH gradient formation, control of urease levels by environmental effectors, and plaque mineralization have been investigated. Microcosm biofilms may be the only useful in vitro systems where the identity of the microbes and processes involved is uncertain. Together, these two approaches begin to capture the complexity of plaque biofilm development, ecology, behavior, and pathology. They facilitate hypothesis testing across almost the whole range of plaque biology and the investigation of antiplaque procedures yielding accurate predictions of plaque behavior in vivo.
天然菌斑及其复杂、异质结构的体内研究存在困难,这促使了实验室生物膜菌斑模型系统的发展。本文概述了其培养技术,并分析了两种以菌斑生物多样性为重点的微生物模型互补方法的原理、优势及相对用途。构建主要菌斑物种的合成菌群生物膜已确定了多种在菌斑形成过程中重要的细菌相互作用。特别是,“马什”九物种生物膜菌群系统是强大的准稳态模型,可进行精确指定、修改和分析。在第二种方法中,微观世界菌斑生物膜在体外从天然口腔微生物群演化为与体内菌斑最密切相关的实验室模型。具有生物多样性的微生物群、异质结构以及与天然菌斑一致的pH行为,可实现功能上可重现的微观世界菌斑。静息pH可通过尿素供应来控制。已经对它们的生长模式、pH梯度形成、环境效应物对脲酶水平的控制以及菌斑矿化进行了研究。微观世界生物膜可能是唯一有用的体外系统,其中涉及的微生物和过程的身份尚不确定。这两种方法共同开始捕捉菌斑生物膜发育、生态、行为和病理学的复杂性。它们有助于在几乎整个菌斑生物学范围内进行假设检验,并有助于研究抗菌斑程序以准确预测体内菌斑行为。