4.2 Article

Adverse biological effects of ingested polystyrene microplastics using Drosophila melanogaster as a model in vivo organism

Publisher

TAYLOR & FRANCIS INC
DOI: 10.1080/15287394.2021.1913684

Keywords

Polystyrene microplastics; Drosophila melanogaster; somatic recombination; climbing assay; risk assessment

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The presence and use of polystyrene microplastics (PSMPs) have raised serious environmental concerns, with unknown impacts on human health. In vivo studies using the Drosophila melanogaster model show that exposure to PSMPs can lead to morphological defects, impaired climbing behavior, and genotoxic effects through somatic DNA recombination in a concentration-dependent manner.
The abundant presence and extensive use of polystyrene microplastics (PSMPs) has recently become a serious environmental concern, as impact of exposure to these substances on human health remains unknown. While in vitro studies yield data on adverse effect of PSMPs, in vivo approaches are more relevant for risk assessment. Drosophila melanogaster is one of the most genetically and experimentally accessible model organisms used in biology as an in vivo model. D. melanogaster was selected as a representative in vivo model organism to examine the genotoxic potential of PSMPs at 5 concentrations of three different sizes namely 4, 10, or 20 mu m. In particular, the wing somatic mutation and recombination test (SMART), a scalable, time-efficient in vivo assay developed to study genotoxicity of various compounds in a rapid manner at low costs was used. The third-instar Drosophila larvae were exposed to PSMPs through food at 5 concentrations ranging from 0.01-10 mM. Viability (lethality), larval length, morphological deformations, locomotor activity (climbing behavior), and genotoxic effects were the end-points measured. Exposure to PSMPs at 4, 10, or 20 mu m produced significant morphological defects, impaired climbing behavior, and genotoxicity as evidenced by the SMART test demonstrating induction of somatic recombination. Significant increases were observed in the frequency of total spots, suggesting that PSMPs might induce genotoxic activity predominantly via initiation of somatic DNA recombination in a concentration-dependent manner.

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