Metabolic heterogeneity and antibiotic susceptibility in biofilms

生物膜中的代谢异质性和抗生素敏感性

• 批准号: 8529188
• 负责人: AARON I PACKMAN
• 金额: $ 34.45万
• 依托单位: NORTHWESTERN UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2010
• 资助国家: 美国
• 起止时间: 2010-09-07 至 2015-08-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8529188
• 关键词: Address; Affect; Antibiotic Therapy; Antibiotic susceptibility; Antibiotics; Antimicrobial Effect; Antimicrobial susceptibility; Catheters; Cell Death; Cells; Chemicals; Communities; Complex; Confocal Microscopy; Coupled; Coupling; Development; Devices; Dyes; Effectiveness; Elements; Environment; Growth; Heterogeneity; Implant; In Situ; Infection; Measurement; Measures; Medical Device; Metabolic; Methods; Microbial Biofilms; Modeling; Mono-S; Morphology; Organism; Orthopedics; Oxygen; Pattern; Predisposition; Process; Relative (related person); Reporter; Simulate; Site; Staining method; Stains; Structure; Surface; System; Time; Velocimetries; Work; antimicrobial; antimicrobial drug; base; design; fluorophore; implantable device; improved; insight; killings; microbial community; model development; novel; particle; pathogen; protective effect; public health relevance; research study; simulation; tool

DESCRIPTION (provided by applicant): Biofilms are microbial communities that grow attached to a surface. Biofilm-based infections occur frequently, and biofilm growth on indwelling devices is very difficult to eradicate. Low rates of antibiotic transport within biofilms, protective effects of the biofilm matrix, and low rates of metabolic activity within the biofilm interior have all been found to contribute to the persistence of these infections, but there is currently little understanding of the processes responsible for these effects. While spatial heterogeneity in biofilms is clearly important to selection of therapy for biofilm-based infections, little information is available on the way in which local environmental conditions influence the development of spatial patterns in biofilms, and hence how the effectiveness of antibiotics varies depending on the body site and type of indwelling device. We hypothesize that spatial patterns of metabolic activity within a biofilm are influenced by spatial patterns in the flow environment, and that these interactions cause biofilm complexity to increase over time. We also hypothesize that the flow environment affects biofilm antimicrobial susceptibility not only by influencing delivery of antimicrobials to cells within the biofilm but also by dictating metabolic gradients within the community. We propose to address these hypotheses through the following specific aims. Aim 1: Observe growth of mono- species biofilms in a planar flow cell in order to assess changes in biofilm morphology, transport patterns, and metabolic activity with increasing spatial variability in environmental flow conditions. Aim 2: Observe the effectiveness of antibiotic treatment in eradicating biofilms having different degrees of spatial complexity, and relate the distribution of local killing efficiency to spatial patterns in transport conditions and metabolic activity. Aim 3: Develop an improved numerical model to allow quantitative analysis of the effects described above. Aim 4: Use the model to clarify multi-scale flow-biofilm interactions, and particularly to evaluate the key features that contribute to the survival of subpopulations of cells in biofilms under antibiotic treatment. We propose to achieve these aims by using a combination of novel experiments and numerical modeling. We will conduct experiments on biofilm growth and treatment in a new experimental system that provides the ability to impose a precisely controlled degree of spatial variability in inflow and outflow patterns. Biofilm growth, changes in flow and oxygen distributions, transport of antibiotic, and the resulting cell death will all be observed directly in situ. We will utilize these new and unique observations to support development of a new numerical model for biofilm development, which will subsequently be used to simulate the effectiveness of antibiotic treatment in eradicating biofilms under different local growth conditions. This combination of measurements and modeling will provide unique insight into the way in which biofilm growth interacts with and modifies the external flow, and ultimately how this complex interaction controls the overall formation of the biofilm and the effects of introduced antimicrobial agents on cells residing in the biofilm matrix. PUBLIC HEALTH RELEVANCE: Metabolic heterogeneity and antibiotic susceptibility in biofilms Summary Narrative Biofilm-based infections of inserted and implanted medical devices such as catheters, neurosurgical devices, and orthopedic devices are difficult to treat. Low rates of antibiotic transport within biofilms, protective effects of the biofilm matrix, and low rates of metabolic activity within the biofilm interior have all been found to contribute to the persistence of these infections, but there is currently little understanding of the processes responsible for these effects. The proposed work will advance understanding of how local environmental conditions influence biofilm growth, and will develop improved tools for assessing the effectiveness of antibiotics against biofilm-based infections.

描述（由申请人提供）：生物膜是附着在表面上生长的微生物群落。基于生物膜的感染经常发生，并且留置装置上生物膜的生长很难根除。生物膜内抗生素转运率低、生物膜基质的保护作用以及生物膜内部代谢活动率低都被发现导致这些感染的持续存在，但目前对造成这些感染的过程知之甚少。影响。虽然生物膜的空间异质性对于基于生物膜的感染的治疗选择显然很重要，但关于当地环境条件如何影响生物膜空间模式的发展以及抗生素的有效性如何根据不同的环境而变化的信息却很少。身体部位和留置装置的类型。我们假设生物膜内代谢活动的空间模式受到流动环境中空间模式的影响，并且这些相互作用导致生物膜复杂性随着时间的推移而增加。我们还假设流动环境不仅通过影响抗菌药物向生物膜内细胞的输送，而且还通过决定群落内的代谢梯度来影响生物膜抗菌敏感性。我们建议通过以下具体目标来解决这些假设。目标 1：观察平面流动池中单物种生物膜的生长，以评估随着环境流动条件的空间变异性的增加，生物膜形态、运输模式和代谢活动的变化。目标 2：观察抗生素治疗消除不同空间复杂程度的生物膜的有效性，并将局部杀灭效率的分布与运输条件和代谢活动的空间模式联系起来。目标 3：开发改进的数值模型，以便对上述影响进行定量分析。目标 4：使用该模型阐明多尺度流-生物膜相互作用，特别是评估有助于抗生素治疗下生物膜中细胞亚群存活的关键特征。我们建议通过结合新颖的实验和数值建模来实现这些目标。我们将在一个新的实验系统中进行生物膜生长和处理的实验，该系统能够在流入和流出模式中施加精确控制的空间变异程度。生物膜的生长、流量和氧气分布的变化、抗生素的运输以及由此产生的细胞死亡都将在原位直接观察。我们将利用这些新的和独特的观察结果来支持开发生物膜形成的新数值模型，该模型随后将用于模拟抗生素治疗在不同局部生长条件下消除生物膜的有效性。这种测量和建模的结合将为生物膜生长与外部流动相互作用并改变外部流动的方式提供独特的见解，以及最终这种复杂的相互作用如何控制生物膜的整体形成以及引入的抗菌剂对驻留于细胞中的细胞的影响。生物膜基质。 公共卫生相关性：生物膜中的代谢异质性和抗生素敏感性 摘要 叙述 插入和植入的医疗器械（例如导管、神经外科器械和骨科器械）的基于生物膜的感染很难治疗。生物膜内抗生素转运率低、生物膜基质的保护作用以及生物膜内部代谢活动率低都被发现导致这些感染的持续存在，但目前对造成这些感染的过程知之甚少。影响。拟议的工作将增进对当地环境条件如何影响生物膜生长的理解，并将开发改进的工具来评估抗生素对生物膜感染的有效性。