Classification of Trypanosoma brucei mammalian life cycle stages using Deep Learning Algorithms
Accurate classification of Trypanosoma brucei bloodstream forms, slender and stumpy, is essential for understanding parasite biology and transmission dynamics. Traditional classification methods rely on flourescent transgenic parasites, as distinguishing these forms visually is highly challenging. T...
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| Published in | PLoS neglected tropical diseases Vol. 19; no. 8; p. e0013298 |
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| Main Authors | , , , , |
| Format | Journal Article |
| Language | English |
| Published |
United States
Public Library of Science
01.08.2025
Public Library of Science (PLoS) |
| Subjects | |
| Online Access | Get full text |
| ISSN | 1935-2735 1935-2727 1935-2735 |
| DOI | 10.1371/journal.pntd.0013298 |
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| Summary: | Accurate classification of Trypanosoma brucei bloodstream forms, slender and stumpy, is essential for understanding parasite biology and transmission dynamics. Traditional classification methods rely on flourescent transgenic parasites, as distinguishing these forms visually is highly challenging. To address this, we developed a semi-automated deep-learning pipeline that segments and classifies T. brucei bloodstream forms from unlabeled microscopic images. The pipeline consists of two key stages: (1) a segmentation step using the Cellpose algorithm, which detects and extracts individual parasites while filtering out artifacts, and (2) a classification step utilizing a deep learning model based on the Xception architecture. The classification model, optimized through transfer learning and fine-tuning, achieved a 97% accuracy, outperforming standard architectures such as InceptionV3, ResNet50, and VGG16. Our results demonstrate the effectiveness of deep learning in parasite stage classification, offering a scalable and efficient approach for high-throughput analysis. Beyond T. brucei, our framework can be adapted for other single-cell classification tasks based on unlabeled morphology, contributing to advancements in biomedical imaging and automated cell analysis. |
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| Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 The authors have declared that no competing interests exist. |
| ISSN: | 1935-2735 1935-2727 1935-2735 |
| DOI: | 10.1371/journal.pntd.0013298 |