Basiry Daniel, Kommedal Roald, Kaster Krista Michelle
Department of Chemistry, Bioscience and Environmental Engineering, Faculty of Science and Technology, University of Stavanger, Stavanger, Norway.
Environ Technol. 2025 Apr;46(10):1612-1624. doi: 10.1080/09593330.2024.2394719. Epub 2024 Aug 30.
As the problem of multi-resistant bacteria grows a better understanding of the spread of antibiotic resistance genes is of utmost importance for society. Wastewater treatment plants contain subinhibitory concentrations of antibiotics and are thought to be hotspots for antibiotic resistance gene propagation. Here we evaluate the influence of sub-minimum inhibitory concentrations of antibiotics on the spread of resistance genes within the bacterial community in activated sludge laboratory-scale sequencing batch reactors. The mixed communities were fed two different ampicillin concentrations (500 and 5000 µg/L) and the reactors were run and monitored for 30 days. During the experiment the β-lactamase resistance gene was monitored via qPCR and DNA samples were taken to monitor the effect of ampicillin on the microbial community. The relative copy number of in the reactor fed with the sub-minimum inhibitory concentration of 500 µg/L ampicillin was spread out over a wider range of values than the control and 5000 µg/L ampicillin reactors indicating more variability of gene number in the 500 µg/L reactor. This result emphasises the problem of sub-minimum inhibitory concentrations of antibiotics in wastewater. High-throughput sequencing showed that continuous exposure to ampicillin caused a shift from a Bacteroidetes to Proteobacteria in the bacterial community. The combined use of qPCR and high-throughput sequencing showed that ampicillin stimulates the spread of resistance genes and leads to the propagation of microbial populations which are resistant to it.
随着多重耐药菌问题的日益严重,更好地了解抗生素抗性基因的传播对社会至关重要。污水处理厂含有亚抑制浓度的抗生素,被认为是抗生素抗性基因传播的热点。在此,我们评估了抗生素亚最小抑制浓度对活性污泥实验室规模序批式反应器中细菌群落内抗性基因传播的影响。混合菌群被投喂两种不同浓度的氨苄青霉素(500和5000 µg/L),反应器运行并监测30天。实验期间,通过定量聚合酶链反应监测β-内酰胺酶抗性基因,采集DNA样本以监测氨苄青霉素对微生物群落的影响。与对照和5000 µg/L氨苄青霉素反应器相比,投喂500 µg/L亚最小抑制浓度氨苄青霉素的反应器中该基因的相对拷贝数分布在更广泛的值范围内,表明500 µg/L反应器中基因数量的变异性更大。这一结果凸显了废水中抗生素亚最小抑制浓度的问题。高通量测序表明,持续接触氨苄青霉素导致细菌群落中从拟杆菌门向变形菌门转变。定量聚合酶链反应和高通量测序的联合使用表明,氨苄青霉素刺激抗性基因的传播,并导致对其具有抗性的微生物种群的增殖。