Johnning Anna, Kristiansson Erik, Fick Jerker, Weijdegård Birgitta, Larsson D G Joakim
Department of Infectious Diseases, Institute of Biomedicine, University of Gothenburg Gothenburg, Sweden ; Department of Mathematical Sciences, Chalmers University of Technology Gothenburg, Sweden.
Department of Mathematical Sciences, Chalmers University of Technology Gothenburg, Sweden.
Front Microbiol. 2015 Dec 9;6:1355. doi: 10.3389/fmicb.2015.01355. eCollection 2015.
Alterations in the target proteins of fluoroquinolones, especially in GyrA and ParC, are known to cause resistance. Here, we investigated environmental Escherichia communities to explore the possible link between the abundance of mutations, and the exposure to fluoroquinolones. Sediment samples were collected from a relatively pristine lake, up and downstream from a sewage treatment plant, and from several industrially polluted sites. The quinolone resistance-determining regions of gyrA and parC were analyzed using amplicon sequencing of metagenomic DNA. Five non-synonymous substitutions were present in all samples, and all of these mutations have been previously linked to fluoroquinolone resistance in Escherichia coli. In GyrA, substitutions S83L and D87N were on average detected at frequencies of 86 and 32%, respectively, and 31% of all amplicons encoded both substitutions. In ParC, substitutions S80I, E84G, and E84V were detected in 42, 0.9, and 6.0% of the amplicons, respectively, and 6.5% encoded double substitutions. There was no significant correlation between the level of fluoroquinolone pollution and the relative abundance of resistance mutations, with the exception of the most polluted site, which showed the highest abundance of said substitutions in both genes. Our results demonstrate that resistance mutations can be common in environmental Escherichia, even in the absence of a fluoroquinolone selective pressure.
已知氟喹诺酮类药物的靶蛋白发生改变,尤其是GyrA和ParC,会导致耐药性。在此,我们对环境中的大肠杆菌群落进行了调查,以探索突变丰度与氟喹诺酮类药物暴露之间的可能联系。从一个相对原始的湖泊、一个污水处理厂的上下游以及几个工业污染场地采集了沉积物样本。使用宏基因组DNA的扩增子测序分析了gyrA和parC的喹诺酮耐药性决定区域。所有样本中均存在5个非同义替换,所有这些突变先前都与大肠杆菌中的氟喹诺酮耐药性有关。在GyrA中,替换S83L和D87N的平均检测频率分别为86%和32%,所有扩增子中有31%编码这两种替换。在ParC中,替换S80I、E84G和E84V分别在42%、0.9%和6.0%的扩增子中被检测到,6.5%的扩增子编码双重替换。除了污染最严重的位点在两个基因中显示出上述替换的丰度最高外,氟喹诺酮污染水平与耐药性突变的相对丰度之间没有显著相关性。我们的结果表明,即使在没有氟喹诺酮选择压力的情况下,耐药性突变在环境大肠杆菌中也可能很常见。