Numerous studies have reported that the toxicity differences
among
metals are widespread; however, little is known about the mechanism
of differences in metal toxicity to aquatic organisms due to the lack
of quantitative understanding of their adverse outcome pathway. Here,
we investigated the effects of Cd and Cu on bioaccumulation, gene
expression, physiological responses, and apical effects in zebrafish
larvae. RNA sequencing was conducted to provide supplementary mechanistic
information for the effects of Cd and Cu exposure. On this basis,
we proposed a quantitative adverse outcome pathway (qAOP) suitable
for metal risk assessment of aquatic organisms. Our work provides
a mechanistic explanation for the differences in metal toxicity where
the strong bioaccumulation of Cu enables the newly accumulated Cu
to reach the threshold that causes different adverse effects faster
than Cd in zebrafish larvae, resulting in a higher toxicity of Cu
than that of Cd. Furthermore, we proposed a parameter C
IT/BCF (the ratio of internal threshold concentration
and bioaccumulation factor) that helps to understand the toxicity
differences by combining the information of bioaccumulation and internal
threshold of adverse effects. This work demonstrated that qAOP is
an effective quantitative tool for understanding the toxicity mechanism
and highlight the importance of toxicokinetics and toxicodynamics
at different biological levels in determining the metal toxicity.