An automated end-to-end system for schistosome viability assessment to accelerate anti-schistosomal drug discovery

Schistosomiasis, a neglected tropical disease affecting millions globally, urgently requires new therapies. Current treatments, like praziquantel (PZQ), face challenges such as drug resistance and ineffectiveness against juvenile parasites. This study develops an automated, high-throughput computational platform to quantify schistosome viability from video data. We introduced an end-to-end system that leverages foundation models in computer vision and fine-tuning to assess schistosome viability from videos. By fine-tuning advanced image segmentation and spatiotemporal feature representation models, our approach accurately captures both morphological and motility-related features of schistosome and maps them to worm viability directly. As a proof of concept, we constructed two datasets (a PZQ-treatment video dataset with 325 videos and a multi-compound treatment video dataset with 245 videos), designed three worm viability assessment tasks and performed extensive evaluation on them. In addition, we developed a schistosome viability scoring tool, which can be accessed online. The system achieved superior predictive accuracy in PZQ-treated worms, with a Pearson correlation coefficient (PCC) of 0.937 for concentration regression, outperforming approaches like hand-crafted feature methods and wrmXpress. A novel 24-hour equivalent PZQ concentration metric was introduced, addressing saturation effects and showing strong generalizability across 13 other compounds (PCC = 0.712). Direct viability score predictions correlated highly with expert assessments, with PCCs of 0.892 for multi-worm analyses and 0.831 for individual worms. We developed a scalable, automated platform for anti-schistosomal drug discovery, providing reliable viability assessments. An accessible online tool enables efficient screening and has broader implications for parasitological research.

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Publication Details

Journal
PLoS neglected tropical diseases
Published
2026-01-09
DOI
https://doi.org/10.1371/journal.pntd.0013865
Primary Topic
Parasites and Host Interactions
Type
article
Field-Weighted Citation Impact
0.00
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article

An automated end-to-end system for schistosome viability assessment to accelerate anti-schistosomal drug discovery

Yuepeng Wang, B Liu, Jipeng Wang, Guangyong Chen et al.
PLoS neglected tropical diseases
Parasites and Host Interactions
article

An automated end-to-end system for schistosome viability assessment to accelerate anti-schistosomal drug discovery

Yuepeng Wang, B Liu, Jipeng Wang, Guangyong Chen, Xiao Zhu, Bian Wu, Wenjun Cheng, Ping Liu
article en

Abstract

Schistosomiasis, a neglected tropical disease affecting millions globally, urgently requires new therapies. Current treatments, like praziquantel (PZQ), face challenges such as drug resistance and ineffectiveness against juvenile parasites. This study develops an automated, high-throughput computational platform to quantify schistosome viability from video data. We introduced an end-to-end system that leverages foundation models in computer vision and fine-tuning to assess schistosome viability from videos. By fine-tuning advanced image segmentation and spatiotemporal feature representation models, our approach accurately captures both morphological and motility-related features of schistosome and maps them to worm viability directly. As a proof of concept, we constructed two datasets (a PZQ-treatment video dataset with 325 videos and a multi-compound treatment video dataset with 245 videos), designed three worm viability assessment tasks and performed extensive evaluation on them. In addition, we developed a schistosome viability scoring tool, which can be accessed online. The system achieved superior predictive accuracy in PZQ-treated worms, with a Pearson correlation coefficient (PCC) of 0.937 for concentration regression, outperforming approaches like hand-crafted feature methods and wrmXpress. A novel 24-hour equivalent PZQ concentration metric was introduced, addressing saturation effects and showing strong generalizability across 13 other compounds (PCC = 0.712). Direct viability score predictions correlated highly with expert assessments, with PCCs of 0.892 for multi-worm analyses and 0.831 for individual worms. We developed a scalable, automated platform for anti-schistosomal drug discovery, providing reliable viability assessments. An accessible online tool enables efficient screening and has broader implications for parasitological research.

PLoS neglected tropical diseasesVol. 20(1)
Fudan University (CN), Zhejiang Lab (CN), Zhejiang Academy of Medical Sciences (CN), Shanghai Drug Administration (CN)
Good health and well-being
Openalex Percentile: Top 91%
Parasites and Host Interactions
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