4.8 Article

Graphene Oxide Inhibits Antibiotic Uptake and Antibiotic Resistance Gene Propagation

Journal

ACS APPLIED MATERIALS & INTERFACES
Volume 8, Issue 48, Pages 33165-33174

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsami.6b09981

Keywords

nanotechnology; pollution control; graphene oxide; sulfamethoxazole; antibiotic resistance genes

Funding

  1. Ministry of Education of China [IRT 13024]
  2. National Natural Science Foundation of China [21307061, 21577070]
  3. Tianjin Natural Science Foundation [14JCQNJC08900]
  4. Specialized Research Fund for the Doctoral Program of Higher Education of China [2013003112016]
  5. Postdoctoral Science Foundation of China [2014M550138, 2015T80215]

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Antibiotics and antibiotic resistance genes (ARGs) in the natural environment have become substantial threats to the ecosystem and public health. Effective strategies to control antibiotics and ARG contaminations are emergent: A novel carbon nanomaterial, graphene oxide (GO), has attracted a substantial amount of attention in environmental fields. This study discovered the inhibition effects of GO on sulfamethoxazole (SMZ) uptake for bacteria and ARG transfer among microorganisms. GO promoted the penetration of SMZ from intracellular to extracellular environments by increasing the cell membrane permeability. In addition, the formation of a GO-SMZ complex reduced the uptake of SMZ in bacteria. Moreover, GO decreased the abundance of the sulI and intI genes by approximately 2-3 orders of magnitude, but the global bacterial activity was not obviously inhibited. A class I integron transfer experiment showed that the transfer frequency was up to SS-fold higher in the control than that of the GO-treated groups. Genetic methylation levels were not significant while sulI gene replication was inhibited. The biological properties of ARGs were altered due to the GO-ARG noncovalent combination, which was confirmed using multiple spectral analyses. This work suggests that GO can potentially be applied for controlling ARG contamination via inhibiting antibiotic uptake and ARG propagation.

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