Exposure of C. elegans eggs to a glyphosate-containing herbicide leads to abnormal neuronal morphology

• Published in: Neurotoxicology and teratology Vol. 55; pp. 23 - 31
• Main Authors: McVey, Kenneth A, Snapp, Isaac B, Johnson, Megan B, Negga, Rekek, Pressley, Aireal S, Fitsanakis, Vanessa A
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 01.05.2016
• Subjects: Animals; C. elegans strain BZ555; C. elegans strain EG1285; Caenorhabditis elegans; Caenorhabditis elegans Proteins - metabolism; DAergic neurons; Emergency; Glycine - analogs & derivatives; Glycine - toxicity; Glyphosate-containing herbicides; Herbicides - toxicity; Medical Education; Nerve Degeneration - chemically induced; Neurites - drug effects; Neurodevelopment; Neurons - drug effects; Neurons - pathology; Organophosphorus Compounds - toxicity; Ovum - drug effects; Ovum - growth & development; Superoxides - metabolism; Touchdown; Neurodevelopment; C. elegans strain BZ555; Glyphosate-containing herbicides; Touchdown; DAergic neurons; C. elegans strain EG1285
• ISSN: 0892-0362; 1872-9738
• DOI: 10.1016/j.ntt.2016.03.002

Abstract Recent data demonstrate that chronic exposure of Caenorhabditis elegans ( C. elegans ) to a high-use glyphosate-containing herbicide, Touchdown (TD), potentially damages the adult nervous system. It is unknown, however, whether unhatched worms exposed to TD during the egg stage show abnormal neurodevelopment post-hatching. Therefore, we investigated whether early treatment with TD leads to aberrant neuronal or neurite development in C. elegans . Studies were completed in three different worm strains with green fluorescent protein (GFP)-tagged neurons to facilitate visual neuronal assessment. Initially, eggs from C. elegans with all neurons tagged with GFP were chronically exposed to TD. Visual inspection suggested decreased neurite projections associated with ventral nerve cord neurons. Data analysis showed a statistically significant decrease in overall green pixel numbers at the fourth larval (L4) stage (* p < 0.05). We further investigated whether specific neuronal populations were preferentially vulnerable to TD by treating eggs from worms that had all dopaminergic (DAergic) or γ-aminobutyric acid (GABAergic) neurons tagged with GFP. As before, green pixel number associated with these discrete neuronal populations was analyzed at multiple larval stages. Data analysis indicated statistically significant decreases in pixel number associated with DAergic, but not GABAergic, neurons (*** p < 0.001) at all larval stages. Finally, statistically significant decreases (at the first larval stage, L1) or increases (at the fourth larval stage, L4) in superoxide levels, a developmental signaling molecule, were detected (* p < 0.05). These data suggest that early exposure to TD may impair neuronal development, perhaps through superoxide perturbation. Since toxic insults during development may late render individuals more vulnerable to neurodegenerative diseases in adulthood, these studies provide some of the first evidence in this model organism that early exposure to TD may adversely affect the developing nervous system.