Non-invasive single-cell morphometry in living bacterial biofilms.
Mingxing ZhangJi ZhangYibo WangJie WangAlecia M AchimovichScott T ActonAndreas GahlmannPublished in: Nature communications (2020)
Fluorescence microscopy enables spatial and temporal measurements of live cells and cellular communities. However, this potential has not yet been fully realized for investigations of individual cell behaviors and phenotypic changes in dense, three-dimensional (3D) bacterial biofilms. Accurate cell detection and cellular shape measurement in densely packed biofilms are challenging because of the limited resolution and low signal to background ratios (SBRs) in fluorescence microscopy images. In this work, we present Bacterial Cell Morphometry 3D (BCM3D), an image analysis workflow that combines deep learning with mathematical image analysis to accurately segment and classify single bacterial cells in 3D fluorescence images. In BCM3D, deep convolutional neural networks (CNNs) are trained using simulated biofilm images with experimentally realistic SBRs, cell densities, labeling methods, and cell shapes. We systematically evaluate the segmentation accuracy of BCM3D using both simulated and experimental images. Compared to state-of-the-art bacterial cell segmentation approaches, BCM3D consistently achieves higher segmentation accuracy and further enables automated morphometric cell classifications in multi-population biofilms.
Keyphrases
- deep learning
- single cell
- convolutional neural network
- cell therapy
- single molecule
- artificial intelligence
- high throughput
- optical coherence tomography
- candida albicans
- machine learning
- pseudomonas aeruginosa
- escherichia coli
- risk assessment
- bone marrow
- high speed
- electronic health record
- loop mediated isothermal amplification
- real time pcr