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Nanoplastic Size Governs the Decoupling of Microbial Survival from Antibiotic Degradation

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In lab tests, a soil bacterium's ability to break down an antibiotic was affected differently by two sizes of plastic nanoparticles. Larger particles delayed bacterial growth but did not slow the breakdown process once it began, while smaller particles entered bacterial cells, caused stress responses, and slowed the breakdown rate by about 40%.

Polymers
Study Type Environmental

Abstract Nanoplastics (NPs) and antibiotics co-occur in wastewater systems, but how NP size influences antibiotic biodegradation by specialized degraders remains unclear. Here, we investigated the effects of europium-doped polystyrene nanoplastics (PS-NPs; PS20 and PS100) on sulfadiazine biodegradation by Arthrobacter sp. strain D2. Modified Gompertz modeling revealed two contrasting inhibition regimes. For PS100, inhibition was dominated by lag-phase prolongation, with no detectable sulfadiazine removal over 48 h at a PS100 concentration of 100 mg L–1. In contrast, PS20 reduced the maximum sulfadiazine degradation rate by ∼40% while causing only minor changes in lag time, indicating rate-dominated inhibition. Quartz crystal microbalance with dissipation monitoring at a model sulfadiazine-enriched interface showed that PS100 markedly reduced the deposition of NP-pre-exposed cells, whereas PS20 only partially impaired adhesion. Transmission electron microscopy coupled with energy-dispersive X-ray spectroscopy further revealed intracellular accumulation of PS20, whereas PS100 remained predominantly extracellular. Phase-specific physiological measurements and transcriptomics suggested that PS20 induced oxidative-stress responses associated with reduced sulfadiazine biodegradation rates, whereas PS100 elicited dose-dependent transcriptional changes during lag-phase extension. Collectively, these findings demonstrate that nanoplastics impair antibiotic attenuation through distinct size-dependent mechanisms involving interface-associated constraints and intracellular interference, highlighting particle size as a key determinant of antibiotic fate in plastic-contaminated wastewater environments.

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