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Effects of erythromycin on biofilm formation and resistance mutation of Escherichia coli on pristine and UV-aged polystyrene microplastics
Summary
Researchers investigated how the antibiotic erythromycin affects bacterial biofilm formation on both new and UV-weathered polystyrene microplastics. They found that UV aging significantly changed the surface properties of the plastic, increasing its ability to absorb antibiotics and promote antibiotic-resistant bacterial mutations. The study suggests that weathered microplastics in the environment may act as hotspots for the development and spread of antibiotic resistance.
Microplastics (MPs) and antibiotics co-occur widely in the environment and pose combined risk to microbial communities. The present study investigated the effects of erythromycin on biofilm formation and resistance mutation of a model bacterium, E. coli, on the surface of pristine and UV-aged polystyrene (PS) MPs sized 1-2 mm. The properties of UV-aged PS were significantly altered compared to pristine PS, with notable increases in specific surface area, carbonyl index, hydrophilicity, and hydroxyl radical content. Importantly, the adsorption capacity of UV-aged PS towards erythromycin was approximately 8-fold higher than that of pristine PS. Biofilms colonizing on UV-aged PS had a greater cell count (5.6 × 10 CFU mg) and a higher frequency of resistance mutation (1.0 × 10) than those on pristine PS (1.4 × 10 CFU mg and 1.4 × 10, respectively). Moreover, erythromycin at 0.1 and 1.0 mg L significantly (p < 0.05) promoted the formation and resistance mutation of biofilm on both pristine and UV-aged PS. DNA sequencing results confirmed that the biofilm resistance was attributed to point mutations in rpoB segment of the bacterial genome. qPCR results demonstrated that both UV aging and erythromycin repressed the expression levels of a global regulator rpoS in biofilm bacteria, as well as two DNA mismatch repair genes mutS and uvrD, which was likely to contribute to increased resistance mutation frequency.
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