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Prenatal Exposure to Herbicide 2,4-Dichlorophenoxyacetic Acid (2,4D) Exacerbates Zika Virus Neurotoxicity In Vitro and In Vivo.
Christoff, Raissa Rilo; da Silva, Débora Santos; Lima, Rafael Ferreira; Franco, Ana Luiza Meneguci Moreira; Higa, Luiza Mendonça; Rossi, Átila Duque; Batista, Carolina; de Andrade, Cherley Borba Vieira; Ortiga-Carvalho, Tania Maria; Ascari, Lucas; de Azevedo Abrahim-Vieira, Bárbara; Bellio, Maria; Tanuri, Amilcar; de Carvalho, Flavia Martinez; Garcez, Patricia Pestana; Lara, Flavio Alves.
Affiliation
  • Christoff RR; Instituto de Ciências Biomédicas, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil.
  • da Silva DS; Laboratorio de Microbiologia Celular, Instituto Oswaldo Cruz, FIOCRUZ, Rio de Janeiro, Brazil.
  • Lima RF; Departamento de Genética, Instituto de Biologia, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil.
  • Franco ALMM; Laboratorio de Epidemiologia das Malformações Congênitas, Instituto Oswaldo Cruz, FIOCRUZ, Rio de Janeiro, Brazil.
  • Higa LM; Programa de Pós-Graduação em Ciências Biológicas (Genética), Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil.
  • Rossi ÁD; Laboratorio de Epidemiologia das Malformações Congênitas, Instituto Oswaldo Cruz, FIOCRUZ, Rio de Janeiro, Brazil.
  • Batista C; Departamento de Genética, Instituto de Biologia, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil.
  • de Andrade CBV; Instituto de Ciências Biomédicas, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil.
  • Ortiga-Carvalho TM; Instituto de Biofísica Carlos Chaga Filho, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil.
  • Ascari L; Instituto de Biofísica Carlos Chaga Filho, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil.
  • de Azevedo Abrahim-Vieira B; Laboratório de Biologia Molecular e Estrutural (LaBiME), Faculdade de Farmácia, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil.
  • Bellio M; Laboratório de Modelagem Molecular & QSAR (ModMolQSAR), Faculdade de Farmácia, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil.
  • Tanuri A; Instituto de Microbiologia Paulo de Góes, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil.
  • de Carvalho FM; Departamento de Genética, Instituto de Biologia, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil.
  • Garcez PP; Laboratorio de Epidemiologia das Malformações Congênitas, Instituto Oswaldo Cruz, FIOCRUZ, Rio de Janeiro, Brazil.
  • Lara FA; Programa de Pós-Graduação em Ciências Biológicas (Genética), Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil.
Environ Toxicol ; 2024 Sep 27.
Article in En | MEDLINE | ID: mdl-39329436
ABSTRACT
Zika virus (ZIKV) infection during pregnancy can lead to a set of congenital malformations known as Congenital ZIKV syndrome (CZS), whose main feature is microcephaly. The geographic distribution of CZS in Brazil during the 2015-2017 outbreak was asymmetrical, with a higher prevalence in the Northeast and Central-West regions of the country, despite the ubiquitous distribution of the vector Aedes aegypti, indicating that environmental factors could influence ZIKV vertical transmission and/or severity. Here we investigate the involvement of the most used agrochemicals in Brazil with CZS. First, we exposed human neuroblastoma SK-N-AS cells to the 15 frequently used agrochemical molecules or derivative metabolites able to cross the blood-brain barrier. We found that a derived metabolite from a widely used herbicide in the Central-West region, 2,4-dichlorophenoxyacetic acid (2,4D), exacerbates ZIKV neurotoxic effects in vitro. We validate this observation by demonstrating vertical transmission leading to microcephaly in the offspring of immunocompetent C57BL/6J mice exposed to water contaminated with 0.025 mg/L of 2,4D. Newborn mice whose dams were exposed to 2,4D and infected with ZIKV presented a smaller brain area and cortical plate size compared to the control. Also, embryos from animals facing the co-insult of ZIKV and 2,4D exposition presented higher Caspase 3 positive cells in the cortex, fewer CTIP2+ neurons and proliferative cells at the ventricular zone, and a higher viral load. This phenotype is followed by placental alterations, such as vessel congestion, and apoptosis in the labyrinth and decidua. We also observed a mild spatial correlation between CZS prevalence and 2,4D use in Brazil's North and Central-West regions, with R2 = 0.4 and 0.46, respectively. Our results suggest that 2,4D exposition facilitates maternal vertical transmission of ZIKV, exacerbating CZS, possibly contributing to the high prevalence of this syndrome in Brazil's Central-West region compared to other regions.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Environ Toxicol Journal subject: SAUDE AMBIENTAL / TOXICOLOGIA Year: 2024 Document type: Article Affiliation country: Brazil Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Environ Toxicol Journal subject: SAUDE AMBIENTAL / TOXICOLOGIA Year: 2024 Document type: Article Affiliation country: Brazil Country of publication: United States