Multigenerational and Transgenerational Effects of Environmentally Relevant Concentrations of Endocrine Disruptors in an Estuarine Fish Model

• Published in: Environmental science & technology Vol. 54; no. 21; pp. 13849 - 13860
• Main Authors: DeCourten, Bethany M, Forbes, Joshua P, Roark, Hunter K, Burns, Nathan P, Major, Kaley M, White, J. Wilson, Li, Jie, Mehinto, Alvine C, Connon, Richard E, Brander, Susanne M
• Format: Journal Article
• Language: English
• Published: United States American Chemical Society 03.11.2020
• Subjects: abnormal development; Animals; Aquatic organisms; bifenthrin; Contaminants; Deoxyribonucleic acid; DNA; DNA methylation; Ecotoxicology and Public Health; Egg production; Endocrine disruptors; Endocrine Disruptors - toxicity; Environmental effects; Epigenetics; Estuaries; estuarine fish; Estuarine pollution; Ethinyl Estradiol - toxicity; Ethinylestradiol; Exposure; Fishes; Gene expression; Immune response; Immune system; Insecticides; larvae; Larval development; Menidia beryllina; Pollutants; Reproduction; technology; toxic substances; Toxicants; Trenbolone; Water Pollutants, Chemical - toxicity
• ISSN: 0013-936X; 1520-5851; 1520-5851
• DOI: 10.1021/acs.est.0c02892

Many pollutants cause endocrine disruption in aquatic organisms. While studies of the direct effects of toxicants on exposed organisms are commonplace, little is known about the potential for toxicant exposures in a parental (F0) generation to affect unexposed F1 or F2 generations (multigenerational and transgenerational effects, respectively), particularly in estuarine fishes. To investigate this possibility, we exposed inland silversides (Menidia beryllina) to environmentally relevant (low ng/L) concentrations of ethinylestradiol, bifenthrin, trenbolone, and levonorgestrel from 8 hpf to 21 dph. We then measured development, immune response, reproduction, gene expression, and DNA methylation for two subsequent generations following the exposure. Larval exposure (F0) to each compound resulted in negative effects in the F0 and F1 generations, and for ethinylestradiol and levonorgestrel, the F2 also. The specific endpoints that were responsive to exposure in each generation varied, but included increased incidence of larval deformities, reduced larval growth and survival, impaired immune function, skewed sex ratios, ovarian atresia, reduced egg production, and altered gene expression. Additionally, exposed fish exhibited differences in DNA methylation in selected genes, across all three generations, indicating epigenetic transfer of effects. These findings suggest that assessments across multiple generations are key to determining the full magnitude of adverse effects from contaminant exposure in early life.