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Artificial-intelligence-driven segmentation and analysis of microbial cells
Shuang Zhang1, Carleton Coffin2, Karyn L Rogers3,4
1Rensselaer Polytechnic Institute, Department of Biomedical Engineering, Troy, New York, United States.
This study introduces an AI system for automated microbial cell analysis, improving efficiency and accuracy in microscopy. The framework enables advanced research on microbial adaptations and extremophiles.
Area of Science:
- Microbiology
- Biotechnology
- Computational Biology
Background:
- Single-cell microbial analysis is crucial for physiology and biotechnology.
- Current manual annotation methods are inefficient and limit scalability.
- Automated quantitative analysis of cell growth and morphology is highly desirable.
Purpose of the Study:
- To develop an AI-driven system for automated microbial cell segmentation and quantitative feature analysis.
- To enable efficient monitoring of cell counts and morphological characteristics without manual annotation.
- To provide a scalable solution for high-throughput microbial cell analysis.
Main Methods:
- A four-component modular system: denoising, zero-shot segmentation (Segment Anything Model - SAM), post-processing, and feature extraction.
- Ablation experiments were conducted to evaluate individual component performance.
- The Segment Anything Model (SAM) with the SAM-H variant was optimized for microbial cell segmentation.
Main Results:
- Denoising and post-processing enhanced segmentation accuracy by 12.10% and 2.30%, respectively.
- The SAM-H model achieved a low average error rate of 3.0% on 1162 annotated *Escherichia coli* cells.
- The system successfully extracted morphometric and intensity features from *E. coli*, yeast, and cancer cell lines.
Conclusions:
- The developed framework automates quantitative analysis of microbial cells in high-resolution microscopy.
- This automation facilitates advanced research into microbial adaptations.
- The system has potential applications in studying extremophiles in challenging environments.
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