PUBLICATION

Developmental toxicity of the fungicide ziram in zebrafish (Danio rerio)

Authors
Cao, F., Souders, C.L., Li, P., Adamovsky, O., Pang, S., Qiu, L., Martyniuk, C.J.
ID
ZDB-PUB-180929-10
Date
2018
Source
Chemosphere   214: 303-313 (Journal)
Registered Authors
Keywords
Dark/light preference, Dopamine system, Gene expression, Mitochondrial bioenergetics, Zebrafish embryos, Ziram
MeSH Terms
  • Animals
  • Behavior, Animal/drug effects
  • Dopamine/genetics
  • Embryo, Nonmammalian/drug effects
  • Embryonic Development/drug effects*
  • Fungicides, Industrial/metabolism
  • Fungicides, Industrial/toxicity
  • Larva/drug effects
  • Locomotion/drug effects
  • Oxidative Stress/genetics
  • Oxygen Consumption/drug effects
  • Zebrafish/growth & development*
  • Zebrafish/metabolism
  • Ziram/toxicity*
PubMed
30265938 Full text @ Chemosphere
CTD
30265938
Abstract
Ziram is a broad spectrum pesticide that belongs to the class of dimethyl-dithiocarbamate (DTC) fungicides. The objectives of this study were to assess the effects of ziram in developing zebrafish. Ziram was highly toxic to zebrafish embryos, with a 96-h LC50 value of 1082.54 nM (∼0.33 mg/L). Zebrafish embryos at 6 h post-fertilization (hpf) were exposed to solvent control (0.1% DMSO), or one dose of 1, 10, 100, and 1000 nM ziram for 96 h. Ziram induced lethality in a dose-dependent manner, decreased hatching rate and heartbeat, and caused wavy deformities at 72 and 96 hpf at 100 and 1000 nM. Basal oxygen consumption rates of zebrafish at 24 hpf were decreased with 1000 nM, suggesting that ziram affects oxidative phosphorylation. We also measured the expression of transcripts associated with the oxidative stress response (sod1 and sod2) and dopamine receptor signaling at ∼96 h of exposure. There was no difference in the expression of genes related to oxidative stress, nor those related to the dopamine system. Locomotor activity was also assessed in larval zebrafish (7 dpf), and ziram increased total activity, the velocity in light zone, and total distance moved at 10 nM, while it decreased the mean time spent in the dark zone at 1 and 10 nM. Behavioral responses were dependent upon the time point and clutch examined. These data demonstrate that ziram negatively impacts embryonic development (i.e. mortality, hatching, heartbeat and notochord development) of zebrafish, decreases basal respiration of embryos, and alters behavioral responses in larvae.
Genes / Markers
Figures
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping