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Applications of Zebrafish Embryo Models to Predict Developmental Toxicity for Agrochemical Product Development.
Bianchi, Enrica; Bhattacharya, Beas; Bowling, Andrew J; Pence, Heather E; Mundy, Paige C; Jones, Gabe; Muriana, Arantza; Grever, William E; Pappas-Garton, Anthony; Sriram, Shreedharan; LaRocca, Jessica; Bondesson, Maria.
  • Bianchi E; Corteva Agriscience, Indianapolis, Indiana 46268, United States.
  • Bhattacharya B; Corteva Agriscience, Indianapolis, Indiana 46268, United States.
  • Bowling AJ; Corteva Agriscience, Indianapolis, Indiana 46268, United States.
  • Pence HE; Corteva Agriscience, Indianapolis, Indiana 46268, United States.
  • Mundy PC; Corteva Agriscience, Indianapolis, Indiana 46268, United States.
  • Jones G; Corteva Agriscience, Indianapolis, Indiana 46268, United States.
  • Muriana A; BBD BioPhenix SLU (BIOBIDE), San Sebastian 20009, Spain.
  • Grever WE; Revvity, Waltham, Massachusetts 02451, United States.
  • Pappas-Garton A; Corteva Agriscience, Indianapolis, Indiana 46268, United States.
  • Sriram S; Corteva Agriscience, Indianapolis, Indiana 46268, United States.
  • LaRocca J; Corteva Agriscience, Indianapolis, Indiana 46268, United States.
  • Bondesson M; Department of Intelligent Systems Engineering, Indiana University, Bloomington, Indiana 47408, United States.
J Agric Food Chem ; 72(32): 18132-18145, 2024 Aug 14.
Article en En | MEDLINE | ID: mdl-39087946
ABSTRACT
The development of safe crop protection products is a complex process that traditionally relies on intensive animal use for hazard identification. Methods that capture toxicity in early stages of agrochemical discovery programs enable a more efficient and sustainable product development pipeline. Here, we explored whether the zebrafish model can be leveraged to identify mammalian-relevant toxicity. We used transgenic zebrafish to assess developmental toxicity following exposures to known mammalian teratogens and captured larval morphological malformations, including bone and vascular perturbations. We further applied toxicogenomics to identify common biomarker signatures of teratogen exposure. The results show that the larval malformation assay predicted teratogenicity with 82.35% accuracy, 87.50% specificity, and 77.78% sensitivity. Similar and slightly lower accuracies were obtained with the vascular and bone assays, respectively. A set of 20 biomarkers were identified that efficiently segregated teratogenic chemicals from nonteratogens. In conclusion, zebrafish are valuable, robust, and cost-effective models for toxicity testing in the early stages of product development.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Columna Vertebral / Agroquímicos Límite: Animals Idioma: En Año: 2024 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Columna Vertebral / Agroquímicos Límite: Animals Idioma: En Año: 2024 Tipo del documento: Article