Development of a High-Content Stem Cell–Focused Drug Screening Platform for Schistosoma mansoni Using Developmentally Advanced Liver Schistosomula: Functional Insights and New Protein Target Leads

⚡ 摘要
作者 Sewwandi Perera; Athina‐Myrto Chioni; Anthony J. Walker 期刊 The Journal of Infectious Diseases 发表日期 2026 ISSN 0022-1899 DOI 10.1093/infdis/jiag392 类型 原创研究 (Original Research)

📄 英文摘要 English Abstract

EN

BACKGROUND: Globally, more than a quarter of a billion people are infected with Schistosoma blood parasites that cause the debilitating disease human schistosomiasis. To assist drug discovery, we developed a novel high content drug screening platform that exploits the extraordinary stem cell biology of the developing parasite. METHOD: Employing non-synchronous in vitro-grown liver stage schistosomula, fluorescence-based staining, confocal laser scanning microscopy, and segmentation of multi-parasite images, the platform was designed to enable high-content quantitative analysis of dividing somatic neoblasts within the parasite to define phenotype. RESULTS: To establish, refine, and test the approach we analysed stem cell proliferation in liver stage schistosomula and validated the impact of EC-144, a compound that supresses Schistosoma neoblast proliferation. Primary drug screening was then done using a stem cell focused library containing 280 compounds, 45 of which attenuated stem cell proliferation by at least 75%. Sixteen 'hit' compounds were prioritised for further testing/confirmation, with testing done in both simple and complex media. Six compounds were finally selected for further investigation, all of which killed or constrained the development of schistosomula and abolished both somatic and germinal stem cell proliferation in adult male and female worms. CONCLUSIONS: In addition to identifying a panel of new anti-schistosomal compounds with associated predicted targets, the findings provide mechanistic insights into the somatic stem cell biology of schistosomes. Further application of this platform, which offers a new approach to assessing compound susceptibility on schistosomula, should accelerate lead compound discovery to help fight human schistosomiasis.

📄 中文摘要 Chinese Abstract

中文
全球有超过2.5亿人感染血吸虫(Schistosoma)血吸虫,该寄生虫导致使人衰弱的人体血吸虫病。为辅助药物发现,我们开发了一种新型高内涵药物筛选……

📋 英文结构化总结 English Structured Summary

摘要整理

EN

Background:

Globally, more than a quarter of a billion people are infected with Schistosoma blood parasites that cause the debilitating disease human schistosomiasis. To assist drug discovery, we developed a novel high content drug sc...

Methods:

To assist drug discovery, we developed a novel high content drug sc...

Results:

N/A - insufficient provided text.

Data Summary:

More than a quarter of a billion people are infected with Schistosoma blood parasites.

Conclusions:

N/A - insufficient provided text.

Practical Significance:

The developed approach is intended to assist drug discovery for human schistosomiasis.

📋 中文结构化总结 Chinese Structured Summary

中文

背景:

全球有超过2.5亿人感染血吸虫(Schistosoma)血吸虫,该寄生虫导致使人衰弱的人体血吸虫病。为辅助药物发现,我们开发了一种新型高内涵药物筛选……

方法:

为辅助药物发现,我们开发了一种新型高内涵药物筛选……

结果:

不适用——提供的文本不足。

数据摘要:

超过2.5亿人感染血吸虫(Schistosoma)血吸虫。

结论:

不适用——提供的文本不足。

实践意义:

所开发的方法旨在辅助人体血吸虫病的药物发现。