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Proteomic analysis in the brain and liver of sea bream (Sparus aurata) exposed to the antibiotics ciprofloxacin, sulfadiazine, and trimethoprim.
Fernandez, Ronield; Colás-Ruiz, Nieves R; Lara-Martín, Pablo A; Fernández-Cisnal, Ricardo; Hampel, Miriam.
Afiliação
  • Fernandez R; Microbiology Research Laboratory, University Simon Bolivar, Carrera 59 No. 59-65, Barranquilla, Colombia; Center for Research and Innovation in Biodiversity and Climate Change (ADAPTIA), University Simón Bolívar, Barranquilla 59-65, Colombia. Electronic address: ronield.fernandez@unisimon.edu.co.
  • Colás-Ruiz NR; Department of Physical Chemistry, Faculty of Marine and Environmental Sciences, University of Cadiz, University Institute for Marine Research (INMAR), 11510, Puerto Real, Spain.
  • Lara-Martín PA; Department of Physical Chemistry, Faculty of Marine and Environmental Sciences, University of Cadiz, University Institute for Marine Research (INMAR), 11510, Puerto Real, Spain.
  • Fernández-Cisnal R; Department of Biochemistry and Molecular Biology, University of Córdoba, Campus Universitario de Rabanales, 14071, Córdoba, Spain.
  • Hampel M; Department of Physical Chemistry, Faculty of Marine and Environmental Sciences, University of Cadiz, University Institute for Marine Research (INMAR), 11510, Puerto Real, Spain.
Environ Pollut ; 356: 124308, 2024 Sep 01.
Article em En | MEDLINE | ID: mdl-38844040
ABSTRACT
Antibiotics, frequently detected in aquatic ecosystems, can negatively impact the health of resident organisms. Although the study on the possible effects of antibiotics on these organisms has been increasing, there is still little information available on the molecular effects on exposed non-target organisms. In our study we used a label free proteomic approach and sea bream, Sparus aurata, to evaluate the effects of exposure to environmentally relevant concentrations of the antibiotic compounds ciprofloxacin (CIP), sulfadiazine (SULF) and trimethoprim (TRIM) produced at the protein level. Individuals of sea bream were exposed to single compounds at 5.2 ± 2.1 µg L-1 of CIP, 3.8 ± 2.7 µg L-1 of SULF and 25.7 ± 10.8 µg L-1 of TRIM for 21 days. After exposure, the number of differentially expressed proteins in the liver was 39, 73 and 4 for CIP, SULF and TRIM respectively. In the brain, there was no alteration of proteins after CIP and TRIM treatment, while 9 proteins were impacted after SULF treatment. The differentially expressed proteins were involved in cellular biological, metabolic, developmental, growth and biological regulatory processes. Overall, our study evidences the vulnerability of Sparus aurata, after exposure to environmentally relevant concentrations of the major antibiotics CIP, SULF and TRIM and that their chronic exposure could lead to a stress situation, altering the proteomic profile of key organs such as brain and liver.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Sulfadiazina / Trimetoprima / Poluentes Químicos da Água / Encéfalo / Ciprofloxacina / Dourada / Proteômica / Fígado / Antibacterianos Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Sulfadiazina / Trimetoprima / Poluentes Químicos da Água / Encéfalo / Ciprofloxacina / Dourada / Proteômica / Fígado / Antibacterianos Idioma: En Ano de publicação: 2024 Tipo de documento: Article