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Deep Learning-Based Automatic Segmentation and Analysis of Mitochondrial Damage by Zika Virus and SARS-CoV-2
Brianda Alexia Agundis-Tinajero1,2, Miguel Ángel Coronado-Ipiña1,2, Ignacio Lara-Hernández2
1Department of Sciences, Autonomous University of San Luis Potosí (UASLP), San Luis Potosí 78295, Mexico.
Abstract:
Viruses can induce various mitochondrial morphological changes, which are associated with the type of immune response. Therefore, characterization and analysis of mitochondrial ultrastructural changes could provide insights into the kind of immune response elicited, especially when compared to uninfected cells. However, this analysis is highly time-consuming and susceptible to observer bias. This work presents the development of a deep learning-based approach for the automatic identification, segmentation, and analysis of mitochondria from thin-section transmission electron microscopy images of cells infected with two SARS-CoV-2 variants or the Zika virus, utilizing a convolutional neural network with a U-Net architecture. A comparison between manual and automatic segmentations, along with morphological metrics, was performed, yielding an accuracy greater than 85% with no statistically significant differences between the manual and automatic metrics. This approach significantly reduces processing time and enables a prediction of the immune response to viral infections by allowing the detection of both intact and damaged mitochondria. Therefore, the proposed deep learning-based tool may represent a significant advancement in the study and understanding of cellular responses to emerging pathogens. Additionally, its applicability could be extended to the analysis of other organelles, thereby opening up new opportunities for automated studies in cell biology.
Insights
A new deep learning tool automatically analyzes mitochondrial changes in virus-infected cells, accurately predicting immune responses. This AI approach speeds up research and aids in understanding cellular responses to pathogens like SARS-CoV-2.
Area of Science:
- Cell Biology
- Virology
- Artificial Intelligence
Background:
- Viral infections induce mitochondrial morphological changes linked to immune responses.
- Analyzing these changes offers insights into cellular immunity but is labor-intensive and prone to bias.
Purpose of the Study:
- To develop a deep learning (DL) approach for automated mitochondrial identification, segmentation, and analysis in virus-infected cells.
- To compare DL-based analysis with manual methods for accuracy and efficiency.
Main Methods:
- Utilized a U-Net convolutional neural network architecture for image analysis.
- Applied the DL model to transmission electron microscopy images of cells infected with SARS-CoV-2 variants and Zika virus.
- Performed comparative analysis of manual versus automated segmentation and morphological metrics.
Main Results:
- Achieved over 85% accuracy in automated mitochondrial segmentation and analysis.
- Demonstrated no statistically significant differences between manual and automated metrics.
- Significantly reduced processing time compared to manual analysis.
Conclusions:
- The DL-based tool accurately and efficiently analyzes mitochondrial ultrastructural changes in viral infections.
- This approach aids in predicting immune responses by detecting intact and damaged mitochondria.
- The tool has potential applications in studying emerging pathogens and automating cell biology research.
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