Effects of nano-TiO2 on antibiotic resistance transfer mediated by RP4 plasmid
Effects of nano-TiO2 on antibiotic resistance transfer mediated by RP4 plasmid
复制标题
纳米TiO对RP4质粒介导的抗生素抗性转移的影响。
DOI:
10.3109/17435390.2014.991429
复制
发表时间:
2015-01-01
期刊:
影响因子:
5
通讯作者:
Li, Jun-Wen
中科院分区:
文献类型:
--
作者:
Qiu, Zhigang;Shen, Zhiqiang;Li, Jun-Wen
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 (TiO2), 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-TiO2 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-TiO2 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-TiO2. According to our model, the presence of nano-TiO2 decreased the bacterial growth rate from 0.0360 to 0.0323 min(-1) and increased the conjugative transfer rate from 6.69 x 10(-12) to 3.93 x 10(-10) mL cell(-1) min(-1). These results indicate that nano-TiO2 inhibited bacterial growth and promoted conjugation simultaneously. The data for morphology and mRNA expression also demonstrated this phenomenon. Our results confirm that environmental nano-TiO2 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.