A KNIME-Based Analysis of the Zebrafish Photomotor Response Clusters the Phenotypes of 14 Classes of Neuroactive Molecules

Recently, the photomotor response (PMR) of zebrafish embryos was reported as a robust behavior that is useful for high-throughput neuroactive drug discovery and mechanism prediction. Given the complexity of the PMR, there is a need for rapid and easy analysis of the behavioral data. In this study, we developed an automated analysis workflow using the KNIME Analytics Platform and made it freely accessible. This workflow allows us to simultaneously calculate a behavioral fingerprint for all analyzed compounds and to further process the data. Furthermore, to further characterize the potential of PMR for mechanism prediction, we performed PMR analysis of 767 neuroactive compounds covering 14 different receptor classes using the KNIME workflow. We observed a true positive rate of 25% and a false negative rate of 75% in our screening conditions. Among the true positives, all receptor classes were represented, thereby confirming the utility of the PMR assay to identify a broad range of neuroactive molecules. By hierarchical clustering of the behavioral fingerprints, different phenotypical clusters were observed that suggest the utility of PMR for mechanism prediction for adrenergics, dopaminergics, serotonergics, metabotropic glutamatergics, opioids, and ion channel ligands.

[1]  Z. Li,et al.  Molecular characterization of the zebrafish P2X receptor subunit gene family , 2003, Neuroscience.

[2]  Louis Saint-Amant,et al.  Development of motor rhythms in zebrafish embryos. , 2010, Progress in brain research.

[3]  Ralf Mikut,et al.  Identification of Nonvisual Photomotor Response Cells in the Vertebrate Hindbrain , 2013, The Journal of Neuroscience.

[4]  Christian Laggner,et al.  Rapid behavior—based identification of neuroactive small molecules in the zebrafish , 2009, Nature chemical biology.

[5]  David Sugden,et al.  Melatonin stimulates cell proliferation in zebrafish embryo and accelerates its development , 2004, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

[6]  S. Haggarty,et al.  Zebrafish Behavioral Profiling Links Drugs to Biological Targets and Rest/Wake Regulation , 2010, Science.

[7]  R. Rodríguez,et al.  The zebrafish: a model to study the endogenous mechanisms of pain. , 2009, ILAR journal.

[8]  F. Macho Sanchez-Simon,et al.  Developmental expression and distribution of opioid receptors in zebrafish , 2008, Neuroscience.

[9]  F. Berardi,et al.  Live imaging reveals a new role for the sigma-1 (σ 1) receptor in allowing microglia to leave brain injuries , 2015, Neuroscience Letters.

[10]  Wolfgang Driever,et al.  Dopamine transporter expression distinguishes dopaminergic neurons from other catecholaminergic neurons in the developing zebrafish embryo , 2001, Mechanisms of Development.

[11]  Robert Levenson,et al.  Identification of zebrafish A2 adenosine receptors and expression in developing embryos. , 2009, Gene expression patterns : GEP.

[12]  M. Wullimann,et al.  Secondary neurogenesis and telencephalic organization in zebrafish and mice: a brief review. , 2009, Integrative zoology.

[13]  Urban Liebel,et al.  Behavioral barcoding in the cloud: embracing data-intensive digital phenotyping in neuropharmacology. , 2012, Trends in biotechnology.

[14]  L. Christophorou Science , 2018, Emerging Dynamics: Science, Energy, Society and Values.

[15]  Michael Schaefer,et al.  Neurotransmitter properties of spinal interneurons in embryonic and larval zebrafish , 2004, The Journal of comparative neurology.

[16]  Thorsten Meinl,et al.  KNIME: The Konstanz Information Miner , 2007, GfKl.

[17]  Thorsten Meinl,et al.  KNIME - the Konstanz information miner: version 2.0 and beyond , 2009, SKDD.

[18]  P. Panula,et al.  Identification of zebrafish histamine H1, H2 and H3 receptors and effects of histaminergic ligands on behavior. , 2007, Biochemical pharmacology.

[19]  J. Fetcho,et al.  Ontogeny and innervation patterns of dopaminergic, noradrenergic, and serotonergic neurons in larval zebrafish , 2004, The Journal of comparative neurology.

[20]  Geoffrey Burnstock,et al.  Embryonic expression of a P2X3 receptor encoding gene in zebrafish , 2000, Mechanisms of Development.

[21]  P Panula,et al.  Development of the histaminergic neurons and expression of histidine decarboxylase mRNA in the zebrafish brain in the absence of all peripheral histaminergic systems , 1998, The European journal of neuroscience.

[22]  Alexander F Schier,et al.  Behavioral screening for neuroactive drugs in zebrafish , 2012, Developmental neurobiology.