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MAPK signaling pathway enhances tolerance of Mytilus galloprovincialis to co-exposure of sulfamethoxazole and polyethylene microplastics
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Researchers exposed Mediterranean mussels to polyethylene microplastics and the antibiotic sulfamethoxazole, both alone and together, to understand their combined effects. The study found that the mussels activated a protective stress-response pathway called MAPK signaling that helped them tolerate the combined pollution, and that DNA damage from the exposure was reversible during a recovery period.
Microplastics (MPs) and antibiotics often coexist in complex marine environments, yet their combined detrimental effects on marine organisms remain underexplored. This study evaluated the effects of polyethylene microplastics (PE, 200 μg/L) and sulfamethoxazole (SMX, 50 μg/L), both individually and in combination, on Mytilus galloprovincialis. The exposure lasted 6 days, followed by a 6-day recovery period. Bioaccumulation, DNA damage, pollutants transport/metabolism related responses and responding alterations of mitogen-activated protein kinase (MAPK) signaling pathway were detected in gills and digestive glands. Bioaccumulation of SMX/PE in mussels occurred in a tissue-specific manner, co-exposure altered SMX contents in investigated tissues. Co-exposure did not induce extra DNA damage, elevated DNA damage was alleviated during the recovery period in all treated groups. The exposure of SMX/PE exerted different alterations in pollutants transport/metabolism related responses, characterized by multixenobiotic resistance and relative expression of key genes (cytochrome P450 monooxygenase, glutathione S-transferase, ATP-binding cassette transporters). Key molecules (p38 MAPK, c-jun N-terminal kinase, extracellular regulated protein kinase, nuclear factor-κB and tumor protein p53) in MAPK signaling pathway were activated at transcriptional and translational levels after SMX/PE and co-exposure. Co-regulation between MAPK members and pollutants transport/metabolism related factors was revealed, suggesting MAPK signaling pathway served as a regulating hub in exposed mussels to conquer SMX/PE stress. Overall, this study provides new insights on SMX/PE induced health risks in marine mussels and potential mechanism through MAPK cascades regulation.
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Researchers exposed Mediterranean mussels to polyethylene microplastics combined with two pharmaceutical drugs and found that the microplastics altered how the drugs accumulated in mussel tissue and changed the organisms' metabolic responses. The combined exposures caused different metabolic disruptions than single exposures, and not all effects were reversed after a recovery period. This highlights how microplastics in the ocean can interact with pharmaceutical pollution to create unexpected biological effects in seafood species.
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Researchers exposed Mediterranean mussels to environmentally collected microplastics from a beach, both alone and combined with the pollutant benzo[a]pyrene, at ecologically relevant concentrations. The study found that even short-term exposure caused cellular and molecular responses in the mussels, and the combination of microplastics with chemical pollutants produced different effects than either contaminant alone.
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Researchers assessed the combined effects of polypropylene microplastics and the pollutant pyrene on Mediterranean mussels over 14 days. They found that while each pollutant individually increased DNA damage, the combination surprisingly did not, suggesting a complex interaction between the two contaminants. However, the combined exposure compromised the mussels' physiological resilience, as shown by their slower heart rate recovery after stress, indicating that co-exposure to microplastics and pollutants can have nuanced biological effects.
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