Silver (nano)materials cause genotoxicity in Enchytraeus crypticus, as determined by the comet assay

Enchytraeids have been used in standard ecotoxicity testing for approximately 20 yr. Since adopting the standard test for survival and reproduction, a number of additional tools have been developed, including transcriptomics and enzymatic biomarkers. So far, a genotoxicity tool and endpoint have not...

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Veröffentlicht in:Environmental toxicology and chemistry 2018-01, Vol.37 (1), p.184-191
Hauptverfasser: Maria, Vera L., Ribeiro, Maria João, Guilherme, Sofia, Soares, Amadeu M.V.M., Scott‐Fordsmand, Janeck J., Amorim, Mónica J.B.
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container_end_page 191
container_issue 1
container_start_page 184
container_title Environmental toxicology and chemistry
container_volume 37
creator Maria, Vera L.
Ribeiro, Maria João
Guilherme, Sofia
Soares, Amadeu M.V.M.
Scott‐Fordsmand, Janeck J.
Amorim, Mónica J.B.
description Enchytraeids have been used in standard ecotoxicity testing for approximately 20 yr. Since adopting the standard test for survival and reproduction, a number of additional tools have been developed, including transcriptomics and enzymatic biomarkers. So far, a genotoxicity tool and endpoint have not been used; hence, the goals of the present study included optimization of the in vivo alkaline comet assay in Enchytraeus crypticus. Further, the effect of silver nanomaterial (Ag NM300K, dispersed, 15 nm) was tested and compared with silver nitrate. Hydrogen peroxide was used as a positive control. The various steps were optimized. The fully detailed standard operating procedure is presented. Silver materials caused genotoxicity, this being differentiated for the nano and non‐nano forms. Silver nitrate caused genotoxicity after 3 d of exposure in a dose‐related manner, although after 7 d the effects were either reduced or repaired. Ag NM300K caused higher genotoxicity after 7 d for the lowest concentration, highlighting a potential nonmonotonic dose–response effect. Overall, the comet assay showed the power to discriminate effects between materials and also toxicity at low relevant doses. Environ Toxicol Chem 2018;37:184–191. © 2017 SETAC
doi_str_mv 10.1002/etc.3944
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Since adopting the standard test for survival and reproduction, a number of additional tools have been developed, including transcriptomics and enzymatic biomarkers. So far, a genotoxicity tool and endpoint have not been used; hence, the goals of the present study included optimization of the in vivo alkaline comet assay in Enchytraeus crypticus. Further, the effect of silver nanomaterial (Ag NM300K, dispersed, 15 nm) was tested and compared with silver nitrate. Hydrogen peroxide was used as a positive control. The various steps were optimized. The fully detailed standard operating procedure is presented. Silver materials caused genotoxicity, this being differentiated for the nano and non‐nano forms. Silver nitrate caused genotoxicity after 3 d of exposure in a dose‐related manner, although after 7 d the effects were either reduced or repaired. Ag NM300K caused higher genotoxicity after 7 d for the lowest concentration, highlighting a potential nonmonotonic dose–response effect. Overall, the comet assay showed the power to discriminate effects between materials and also toxicity at low relevant doses. 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source Wiley Online Library Journals Frontfile Complete
subjects Bioassays
Biocompatibility
Biomarkers
Comet assay
Damage detection
Enchytraeus crypticus
Genetic damage indicator (GDI)
Genotoxicity
Hydrogen peroxide
In vivo methods and tests
Metallic nanoparticle
Nanomaterials
Silver
Silver nitrate
Single‐cell gel electrophoresis (SCGE)
Soil invertebrate
Toxicity
Toxicity testing
title Silver (nano)materials cause genotoxicity in Enchytraeus crypticus, as determined by the comet assay
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