PUBLICATION

Systematic developmental toxicity assessment of a structurally diverse library of PFAS in zebrafish

Authors
Truong, L., Rericha, Y., Thunga, P., Marvel, S., Wallis, D., Simonich, M.T., Field, J.A., Cao, D., Reif, D.M., Tanguay, R.L.
ID
ZDB-PUB-220311-9
Date
2022
Source
Journal of hazardous materials   431: 128615 (Journal)
Registered Authors
Tanguay, Robyn L.
Keywords
Abnormal behavior, Developmental toxicity, PFAS, Structure-activity relationship, Zebrafish
MeSH Terms
  • Animals
  • Fluorocarbons*/analysis
  • Larva
  • Teratogens
  • Zebrafish*
PubMed
35263707 Full text @ J. Hazard. Mater.
Abstract
Per- and polyfluoroalkyl substances (PFAS) are a class of widely used chemicals with limited human health effects data relative to the diversity of structures manufactured. To help fill this data gap, an extensive in vivo developmental toxicity screen was performed on 139 PFAS provided by the US EPA. Dechorionated embryonic zebrafish were exposed to 10 nominal water concentrations of PFAS (0.015-100 µM) from 6 to 120 h post-fertilization (hpf). The embryos were assayed for embryonic photomotor response (EPR), larval photomotor response (LPR), and 13 morphological endpoints. A total of 49 PFAS (35%) were bioactive in one or more assays (11 altered EPR, 25 altered LPR, and 31 altered morphology). Perfluorooctanesulfonamide (FOSA) was the only structure that was bioactive in all 3 assays, while Perfluorodecanoic acid (PFDA) was the most potent teratogen. Low PFAS volatility was associated with developmental toxicity (p < 0.01), but no association was detected between bioactivity and five other physicochemical parameters. The bioactive PFAS were enriched for 6 supergroup chemotypes. The results illustrate the power of a multi-dimensional in vivo platform to assess the developmental (neuro)toxicity of diverse PFAS and in the acceleration of PFAS safety research.
Genes / Markers
Figures
Show all Figures
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping