4.8 Article

Impact of Plastic Particles on the Horizontal Transfer of Antibiotic Resistance Genes to Bacterium: Dependent on Particle Sizes and Antibiotic Resistance Gene Vector Replication Capacities

Journal

ENVIRONMENTAL SCIENCE & TECHNOLOGY
Volume 56, Issue 21, Pages 14948-14959

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.est.2c00745

Keywords

plastic particles; antibiotic resistance genes; horizontal gene transfer; transformation; cell membrane; DNA replication

Funding

  1. National Natural Science Foundation of China
  2. Natural Science Foundation of Jiangsu Province of China
  3. National Science Foundation for Postdoctoral Scientists of China
  4. [42107024]
  5. [41925029]
  6. [41877125]
  7. [22161132011]
  8. [BK20210413]
  9. [2021M691609]

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This study explored the impact of polystyrene particles with different sizes on the horizontal gene transfer of antibiotic resistance genes (ARGs) mediated by plasmids into Escherichia coli cells. The results showed that small particles had an effect on the transfer of ARGs, while large particles did not. The effects of particles on plasmid transfer varied depending on the plasmid's replication capacity. The mechanisms involved direct interaction with membrane lipids and interference with plasmid replication. This study contributes to our understanding of the environmental dissemination of ARGs in plastic contamination.
Plastic particles impact the propagation of antibiotic resistance genes (ARGs) in environmental media, and their perturbation on the horizontal gene transfer (HGT) of ARGs is recognized as a critical influencing mechanism. However, studies concerning the influence and influencing mechanisms of plastic particles on the HGT of ARGs were limited, particularly for the effect of particle sizes and ARG vector-associated mechanisms. This study explored the impact of polystyrene (PS) particles with sizes of 75, 90, 100, 1000, and 10000 nm on the HGT (via transformation) of ARGs mediated by pUC19, pSTV29, and pBR322 plasmids into Escherichia coli cells. PS particles with sizes <= 100 nm impacted the transformation of ARGs, but large particles (1000 and 10000 nm) showed no obvious effects. Effects of PS particles on the transfer of three plasmids were vastly distinct. For pUC19 with high replication capacities, the transfer was monotonously promoted. However, for pSTV29 and pBR322 with low replication capacities, suppressing effects were observed. This was attributed to two competing mechanisms. The enhancing mechanism was that the direct interaction of PS particles with membrane lipids and the indirect effect associated with bacterial oxidative stress response induced pore formation on the cell membrane and increased membrane permeability, thus enhancing plasmid entrance. The inhibiting mechanism was that PS particles interfered with plasmid replication inside E. coli, thus decreasing the bacterial tranformation. This study deepened our understanding of the environmental dissemination of ARGs in plastic contamination.

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