Publication | Closed Access
Effects of nano-TiO<sub>2</sub>on antibiotic resistance transfer mediated by RP4 plasmid
90
Citations
39
References
2015
Year
EngineeringEscherichia ColiEnvironmental BiotechnologyAntibiotic ResistanceAntibiotic Resistance GenesDrug ResistancePhotocatalysisEnvironmental MicrobiologyInfection ControlAntimicrobial ResistanceNanobiotechnologyAntibacterial AgentAntimicrobial CompoundBacterial ResistanceClinical MicrobiologyConjugation ProcessAntimicrobial Resistance GeneAntimicrobial SusceptibilityAntibioticsBiotechnologySynthetic BiologyMicrobiologyAntibiotic Resistance TransferMedicine
The potential risks of nano-materials and the spread of antibiotic resistance genes (ARGs) have become two major global public concerns. Studies have confirmed that nano-alumina can promote the spread of ARGs mediated by plasmids. Nano-titanium dioxide (TiO(2)), an excellent photocatalytic nano-material, has been widely used and is often present in aqueous environments. At various nano-material concentrations, bacterial density, matting time, and matting temperature, nano-TiO(2) can significantly promote the conjugation of RP4 plasmid in Escherichia coli. We developed a mathematical model to quantitatively describe the conjugation process and used this model to evaluate the effects of nano-TiO(2) on the spread of ARGs. We obtained analytical solutions for total and resistant bacteria, which were enumerated by the abundance of genetic loci unique to the plasmid and the chromosome using qPCR. Our results showed that the mathematic model was able to fit the experimental data well and can be used to quantitatively evaluate the effects of nano-TiO(2). According to our model, the presence of nano-TiO(2) decreased the bacterial growth rate from 0.0360 to 0.0323 min(-1) and increased the conjugative transfer rate from 6.69 × 10(-12) to 3.93 × 10(-10 )mL cell(-1) min(-1). These results indicate that nano-TiO(2) inhibited bacterial growth and promoted conjugation simultaneously. The data for morphology and mRNA expression also demonstrated this phenomenon. Our results confirm that environmental nano-TiO(2) may cause the spread of ARGs and thus poses an environmental risk. In addition, we provide a potential method for monitoring changes in ARGs that result from conjugation and evaluating the effects of antimicrobial substances on ARG expression.
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