Pettygrove Brian A, Smith Heidi J, Pallister Kyler B, Voyich Jovanka M, Stewart Philip S, Parker Albert E
Center for Biofilm Engineering, Montana State University, Bozeman, MT, United States.
Department of Microbiology and Cell Biology, Montana State University, Bozeman, MT, United States.
Front Microbiol. 2022 Jan 13;12:785182. doi: 10.3389/fmicb.2021.785182. eCollection 2021.
The goal of this study was to quantify the variability of confocal laser scanning microscopy (CLSM) time-lapse images of early colonizing biofilms to aid in the design of future imaging experiments. To accomplish this a large imaging dataset consisting of 16 independent CLSM microscopy experiments was leveraged. These experiments were designed to study interactions between human neutrophils and single cells or aggregates of () during the initial stages of biofilm formation. Results suggest that in untreated control experiments, variability differed substantially between growth phases (i.e., lag or exponential). When studying the effect of an antimicrobial treatment (in this case, neutrophil challenge), regardless of the inoculation level or of growth phase, variability changed as a frown-shaped function of treatment efficacy (i.e., the reduction in biofilm surface coverage). These findings were used to predict the best experimental designs for future imaging studies of early biofilms by considering differing (i) numbers of independent experiments; (ii) numbers of fields of view (FOV) per experiment; and (iii) frame capture rates per hour. A spreadsheet capable of assessing any user-specified design is included that requires the expected mean log reduction and variance components from user-generated experimental results. The methodology outlined in this study can assist researchers in designing their CLSM studies of antimicrobial treatments with a high level of statistical confidence.
本研究的目的是量化早期定殖生物膜的共聚焦激光扫描显微镜(CLSM)延时图像的变异性,以帮助设计未来的成像实验。为实现这一目标,利用了一个由16个独立的CLSM显微镜实验组成的大型成像数据集。这些实验旨在研究生物膜形成初始阶段人类中性粒细胞与单个细胞或()聚集体之间的相互作用。结果表明,在未处理的对照实验中,不同生长阶段(即迟缓期或指数期)的变异性存在显著差异。在研究抗菌处理(在本案例中为中性粒细胞攻击)的效果时,无论接种水平或生长阶段如何,变异性都作为处理效果(即生物膜表面覆盖率的降低)的皱眉形函数而变化。通过考虑不同的(i)独立实验数量;(ii)每个实验的视野(FOV)数量;以及(iii)每小时的帧捕获率,这些发现被用于预测未来早期生物膜成像研究的最佳实验设计。包含一个能够评估任何用户指定设计的电子表格,该表格需要用户生成的实验结果中的预期平均对数减少量和方差分量。本研究中概述的方法可以帮助研究人员以高度的统计置信度设计他们关于抗菌处理的CLSM研究。