Relaxation-weighted MRI analysis of biofilm EPS: Differentiating biopolymers, cells, and water

IF 5.9 Q1 MICROBIOLOGY Biofilm Pub Date : 2024-10-24 DOI:10.1016/j.bioflm.2024.100235
Matthew R. Willett , Sarah L. Codd , Joseph D. Seymour , Catherine M. Kirkland
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Abstract

Biofilms are a highly complex community of microorganisms embedded in a protective extracellular polymeric substance (EPS). Successful biofilm control requires a variety of approaches to better understand the structure-function relationship of the EPS matrix. Magnetic resonance imaging (MRI) is a versatile tool which can measure spatial structure, diffusion, and flow velocities in three dimensions and in situ. It is well-suited to characterize biofilms under natural conditions and at different length scales. MRI contrast is dictated by T1 and T2 relaxation times which vary spatially depending on the local chemical and physical environment of the sample. Previous studies have demonstrated that MRI can provide important insights into the internal structure of biofilms, but the contribution of major biofilm components—such as proteins, polysaccharides, and cells—to MRI contrast is not fully understood. This study explores how these components affect contrast in T1-and T2-weighted MRI by analyzing artificial biofilms with well-defined properties modeled after aerobic granular sludge (AGS), compact spherical biofilm aggregates used in wastewater treatment. MRI of these biofilm models showed that certain gel-forming polysaccharides are a major source of T2 contrast, while other polysaccharides show minimal contrast. Proteins were found to reduce T2 contrast slightly when combined with polysaccharides, while cells had a negligible impact on T2 but showed T1 contrast. Patterns observed in the model biofilms served as a reference for examining T2 and T1-weighted contrast in the void spaces of two distinct AGS granules, allowing for a qualitative evaluation of the EPS components which may be present. Further insights provided by MRI may help improve understanding of the biofilm matrix and guide how to better manage biofilms in wastewater, clinical, and industrial settings.
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生物膜 EPS 的松弛加权磁共振成像分析:区分生物聚合物、细胞和水
生物膜是嵌入保护性胞外聚合物物质(EPS)的高度复杂的微生物群落。要成功控制生物膜,需要采用多种方法来更好地了解 EPS 基质的结构与功能关系。磁共振成像(MRI)是一种多功能工具,可在原位测量三维空间结构、扩散和流速。它非常适合在自然条件下以不同的长度尺度描述生物膜的特征。核磁共振成像的对比度由 T1 和 T2 松弛时间决定,而 T1 和 T2 松弛时间随样本当地的化学和物理环境而在空间上变化。以往的研究表明,核磁共振成像可为了解生物膜的内部结构提供重要信息,但人们对生物膜的主要成分(如蛋白质、多糖和细胞)对核磁共振成像对比度的影响还不完全了解。本研究以废水处理中使用的致密球形生物膜聚集体--好氧颗粒污泥(AGS)为模型,分析了具有明确性质的人工生物膜,从而探讨了这些成分如何影响 T1 和 T2 加权核磁共振成像的对比度。这些生物膜模型的核磁共振成像显示,某些凝胶形成的多糖是 T2 对比度的主要来源,而其他多糖显示的对比度很小。研究发现,蛋白质与多糖结合会略微降低 T2 对比度,而细胞对 T2 的影响可以忽略不计,但会显示出 T1 对比度。在模型生物膜中观察到的模式可作为参考,用于检查两种不同 AGS 颗粒空隙中的 T2 和 T1 加权对比度,从而对可能存在的 EPS 成分进行定性评估。核磁共振成像提供的进一步见解可能有助于加深对生物膜基质的了解,并指导如何更好地管理废水、临床和工业环境中的生物膜。
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来源期刊
Biofilm
Biofilm MICROBIOLOGY-
CiteScore
7.50
自引率
1.50%
发文量
30
审稿时长
57 days
期刊介绍:
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