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How nanoscale plastics facilitate the evolution of antibiotic resistance?

Journal of Hazardous Materials 2024 4 citations ? Citation count from OpenAlex, updated daily. May differ slightly from the publisher's own count. Score: 55 ? 0–100 AI score estimating relevance to the microplastics field. Papers below 30 are filtered from public browse.
Yan Xu, Houyu Li, Wei Liu Houyu Li, Wei Liu Houyu Li, Houyu Li, Yuqiang Ding, Wei Liu Wei Liu Yuqiang Ding, Yuqiang Ding, Wei Liu Houyu Li, Wei Liu Wei Liu Dandan Zhang, Wei Liu Wei Liu Wei Liu Wei Liu Wei Liu Wei Liu Houyu Li, Wei Liu Wei Liu Wei Liu Wei Liu Wei Liu

Summary

Researchers explored how nanoscale plastic particles promote the evolution of antibiotic resistance in bacteria. They found that exposure to nanoplastics increased oxidative stress in bacteria, which in turn accelerated mutations and horizontal gene transfer that confer resistance to antibiotics. The study suggests that nanoplastic pollution could be an overlooked factor contributing to the global antibiotic resistance crisis.

The plastic can enhance the proliferation of antibiotic resistance genes (ARGs), however, the effect of nanoplastics (NPLs) on bacterial antibiotic resistance has not been clearly explained. Herein, we explored the effects and mechanisms of NPLs of different sizes (200 and 600 nm) on the evolution of antibiotic resistance in Serratia marcescens. The results indicated that the evolution of bacterial antibiotic resistance could be promoted under NPLs exposure, which the median of relative abundance of ARGs was 1.11-1.46 times compared to the treatment without NPLs. Transcriptomic analysis showed that the larger size of NPLs mainly increased the permeability of bacterial cell membranes to efflux antibiotics, thus potentiating antibiotic resistance. While, the smaller NPLs is more than that, its enhanced the expression of antibiotic resistance by modulating bacterial metabolic processes. The genome SNP analysis found that the NPLs could cause the genetic mutation occurrence to alter the membrane transport and metabolism processes, and it increased at a size of 200 nm more than at 600 nm NPLs. Importantly, we demonstrated that the horizontal transfer of ARGs was augmented due to the NPLs could dock to bacterial surface proteins and pull their movement to contact with other bacteria (binding energy of membrane proteins: -8.54 kcal/mol), especially the smaller size. It suggests that NPLs will also contribute to the proliferation of ARGs in the environment. This study provides data for understanding the risk of bacterial resistance.

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