Lim Chun Ping, Mai Phuong Nguyen Quoc, Roizman Sade Dan, Lam Yee Cheong, Cohen Yehuda
Singapore Centre for Environmental Life Sciences Engineering (SCELSE), Nanyang Technological University, Singapore.
The School of Mechanical and Aerospace Engineering, Nanyang Technological University, Singapore.
NPJ Biofilms Microbiomes. 2016 Oct 19;2:16023. doi: 10.1038/npjbiofilms.2016.23. eCollection 2016.
Life of bacteria is governed by the physical dimensions of life in microscales, which is dominated by fast diffusion and flow at low Reynolds numbers. Microbial biofilms are structurally and functionally heterogeneous and their development is suggested to be interactively related to their microenvironments. In this study, we were guided by the challenging requirements of precise tools and engineered procedures to achieve reproducible experiments at high spatial and temporal resolutions. Here, we developed a robust precise engineering approach allowing for the quantification of real-time, high-content imaging of biofilm behaviour under well-controlled flow conditions. Through the merging of engineering and microbial ecology, we present a rigorous methodology to quantify biofilm development at resolutions of single micrometre and single minute, using a newly developed flow cell. We designed and fabricated a high-precision flow cell to create defined and reproducible flow conditions. We applied high-content confocal laser scanning microscopy and developed image quantification using a model biofilm of a defined opportunistic strain, OUS82. We observed complex patterns in the early events of biofilm formation, which were followed by total dispersal. These patterns were closely related to the flow conditions. These biofilm behavioural phenomena were found to be highly reproducible, despite the heterogeneous nature of biofilm.
细菌的生命受微观尺度下生命的物理维度支配,这主要由低雷诺数下的快速扩散和流动主导。微生物生物膜在结构和功能上具有异质性,其发育被认为与其微环境存在交互关系。在本研究中,我们遵循精确工具和工程程序的挑战性要求,以在高空间和时间分辨率下实现可重复的实验。在此,我们开发了一种强大的精确工程方法,可在良好控制的流动条件下对生物膜行为进行实时、高内涵成像定量分析。通过将工程学与微生物生态学相结合,我们提出了一种严谨的方法,使用新开发的流动小室,在单微米和单分钟分辨率下对生物膜发育进行定量分析。我们设计并制造了一个高精度流动小室,以创建确定且可重复的流动条件。我们应用高内涵共聚焦激光扫描显微镜,并使用一种确定的机会性菌株OUS82的模型生物膜开发图像定量分析方法。我们观察到生物膜形成早期事件中的复杂模式,随后是完全分散。这些模式与流动条件密切相关。尽管生物膜具有异质性,但这些生物膜行为现象被发现具有高度可重复性。