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Quantitative Analysis of Per- and Polyfluoroalkyl Substances (PFAS) in Selective South Bay Water Bodies
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Researchers exposed tiny worms called C. elegans to polystyrene microplastics of two sizes and concentrations for 24 hours. Worms genetically engineered to glow when DNA damage occurs showed increased glowing after exposure, suggesting the microplastics triggered a DNA damage response in these worms.
DNA damage is a key driver of genetic mutations and disease, including cancer.Microplastics, generated from the degradation of plastic waste, are now widely detected in water, food, and the human body.However, their potential to induce DNA damage remains largely unknown.Here, we examined the effect of polystyrene microplastics on causing DNA damage using Caenorhabditis elegans (C.elegans) as a model organism.Transgenic cep-1::GFP worms, which express green fluorescent protein (GFP) under the control of the cep-1 promoter in response to DNA damage, were exposed to polystyrene beads of two sizes (0.2 µm or 1 µm) at two concentrations (1 × 10⁷ particles/mL and 1 × 10⁸ particles/mL) for 24 hours.Wild-type and untreated transgenic worms served as controls.GFP expression was quantified by fluorescence microscopy and ImageJ analysis.Microplastic exposure significantly elevated GFP expression in cep-1::GFP worms regardless of microplastic size or concentration, suggesting robust induction of DNA damage response, whereas neither control group showed a significant response.Altogether, these results demonstrate that polystyrene microplastics can induce DNA damage in C. elegans and suggest that similar genotoxic effects may occur in other organisms, including humans, highlighting a potential link between microplastic exposure and disease pathogenesis.
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Cellular toxicity and apoptosis-related responses to individual and combined exposure to microplastics and perfluorooctane sulfonic acid (PFOS) in Hediste diversicolor coelomocytes.
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Marine worms (Hediste diversicolor) were exposed to microplastics and PFOS, a persistent chemical, in sediment for 7 days. Combined exposure increased PFOS buildup in body fluid and caused cell damage, DNA damage, and changes in genes linked to cell death, with effects varying by measurement and chemical dose.
Exposure to polystyrene microplastics and perfluorooctane sulfonate disrupt the homeostasis of intact planarians and the growth of regenerating planarians
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This study tested how polystyrene microplastics and PFOS (a "forever chemical") affect flatworms both individually and together. The combination caused greater DNA damage, disrupted nerve development, and interfered with the worms' ability to regenerate. Since microplastics can absorb and carry chemicals like PFOS, this research highlights how plastic pollution may amplify the toxicity of other environmental contaminants.
Biochemical and physiological effects of multigenerational exposure to spheric polystyrene microplastics in Caenorhabditis elegans
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Researchers found that multigenerational exposure of C. elegans to polystyrene microplastics at low concentrations triggered oxidative stress, increased detoxification enzyme activity, and caused accumulating physiological effects across five consecutive generations.
Aged polystyrene microplastics cause reproductive impairment via DNA-damage induced apoptosis in Caenorhabditis elegans
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Researchers found that sunlight-aged polystyrene microplastics caused significantly more reproductive damage than fresh microplastics in a laboratory worm model. The aged particles triggered DNA damage and programmed cell death in reproductive tissue through a specific signaling pathway. This matters because microplastics in the real environment are typically weathered by sunlight, making them potentially more harmful to fertility than laboratory studies using new plastics would suggest.
Combined exposure to microplastics and PFASs on earthworms: size and concentration effects
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Researchers co-exposed earthworms to polystyrene microplastics of two sizes (30 nm and 10 µm) and PFAS compounds for 21 days, finding that combined exposure suppressed growth rates by 65% relative to controls, caused more severe intestinal and epidermal tissue damage, amplified oxidative stress markers, and disrupted gut microbiota more than either contaminant alone—with nanoscale MPs producing the strongest effects.
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