A versatile, automated and high-throughput drug screening platform for zebrafish embryos

Author:

Lubin Alexandra1ORCID,Otterstrom Jason2ORCID,Hoade Yvette1,Bjedov Ivana3ORCID,Stead Eleanor3,Whelan Matthew4ORCID,Gestri Gaia5ORCID,Paran Yael2ORCID,Payne Elspeth1ORCID

Affiliation:

1. Research Department of Haematology, Cancer Institute, University College London, London WC1E 6DD, UK

2. IDEA Bio-Medical Ltd., Rehovot 76705, Israel

3. Research Department of Cancer Biology, Cancer Institute, University College London, London WC1E 6DD, UK

4. Division of Infection and Immunity, University College London, London WC1E 6BT, UK

5. Department of Cell and Developmental Biology, University College London, London WC1E 6AR, UK

Abstract

ABSTRACT Zebrafish provide a unique opportunity for drug screening in living animals, with the fast-developing, transparent embryos allowing for relatively high-throughput, microscopy-based screens. However, the limited availability of rapid, flexible imaging and analysis platforms has limited the use of zebrafish in drug screens. We have developed an easy-to-use, customisable automated screening procedure suitable for high-throughput phenotype-based screens of live zebrafish. We utilised the WiScan® Hermes High Content Imaging System to rapidly acquire brightfield and fluorescent images of embryos, and the WiSoft® Athena Zebrafish Application for analysis, which harnesses an Artificial Intelligence-driven algorithm to automatically detect fish in brightfield images, identify anatomical structures, partition the animal into regions and exclusively select the desired side-oriented fish. Our initial validation combined structural analysis with fluorescence images to enumerate GFP-tagged haematopoietic stem and progenitor cells in the tails of embryos, which correlated with manual counts. We further validated this system to assess the effects of genetic mutations and X-ray irradiation in high content using a wide range of assays. Further, we performed simultaneous analysis of multiple cell types using dual fluorophores in high throughput. In summary, we demonstrate a broadly applicable and rapidly customisable platform for high-content screening in zebrafish. This article has an associated First Person interview with the first author of the paper.

Funder

Cancer Research UK

IDEA Bio-Medical

European Research Council

University College London Hospitals Biomedical Research Centre

Medical Research Council

Publisher

The Company of Biologists

Subject

General Agricultural and Biological Sciences,General Biochemistry, Genetics and Molecular Biology

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