Biological and Nanoscale Systems Group, Biosciences Division, Oak Ridge National Laboratory, Oak Ridge, TN 37831, USA; Center for Aerosol and Nanomaterials Engineering, RTI International, Research Triangle Park, NC 27709, USA.
Int J Antimicrob Agents. 2013 Nov;42(5):462-5. doi: 10.1016/j.ijantimicag.2013.07.007. Epub 2013 Aug 15.
Enteroaggregative Escherichia coli (EAEC) causes diarrhoea. The antibiotic of choice for treating EAEC infections is ciprofloxacin. EAEC differs from other subgroups of pathogenic E. coli by having a surface protein, dispersin, which has previously been shown to play an important role in ciprofloxacin susceptibility for EAEC model strain 042. To investigate further the role of dispersin in ciprofloxacin susceptibility, minimum inhibitory concentrations (MICs) were determined for 25 clinical isolates, including 15 with dispersin and 10 without. Dispersin-positive strains had a lower MIC than dispersin-negative strains. The mechanism of action behind this observation may be caused by dispersin (i) increasing the bacteria-antibiotic interaction or (ii) facilitating ciprofloxacin access to the intracellular target, DNA gyrase/topoisomerase. To test the role of dispersin in ciprofloxacin sensitivity, EAEC 042 as well as its isogenic mutants, dispersin mutant (042aap) and a mutant in the transporter apparatus gene aatA, believed to be involved in dispersin transport to the bacterial surface (042aatA), were utilised. As predicted, 042 had a higher sensitivity to ciprofloxacin than 042aap, but it was also found that the MIC of 042aatA was similar to 042aap. To address the question of the role of dispersin in ciprofloxacin susceptibility, the concentration of ciprofloxacin bound in biofilms of 042 and 042aap was quantified by treating bacteria with radiolabelled 2-(14)C-ciprofloxacin. The results showed that dispersin did not increase the amount of bound ciprofloxacin as a function of biomass, indicating instead that dispersin facilitates ciprofloxacin access to the intracellular target leading to increased antibiotic susceptibility.
肠聚集性大肠杆菌(EAEC)可引起腹泻。治疗 EAEC 感染的首选抗生素是环丙沙星。EAEC 与其他致病性大肠杆菌亚群不同,它具有一种表面蛋白,即分散素,先前已表明该蛋白在 EAEC 模型株 042 的环丙沙星敏感性中起重要作用。为了进一步研究分散素在环丙沙星敏感性中的作用,测定了 25 株临床分离株的最小抑菌浓度(MIC),其中 15 株具有分散素,10 株没有。具有分散素的菌株的 MIC 低于不具有分散素的菌株。这种观察结果的作用机制可能是分散素 (i) 增加了细菌-抗生素相互作用,或 (ii) 促进了环丙沙星进入细胞内靶标,即 DNA 回旋酶/拓扑异构酶。为了测试分散素在环丙沙星敏感性中的作用,使用了 EAEC 042 及其同源突变体,分散素突变体(042aap)和一种被认为参与分散素向细菌表面转运的转运器基因 aatA 突变体(042aatA)。正如预期的那样,042 对环丙沙星的敏感性高于 042aap,但也发现 042aatA 的 MIC 与 042aap 相似。为了解决分散素在环丙沙星敏感性中的作用问题,通过用放射性标记的 2-(14)C-环丙沙星处理细菌,定量测定了 042 和 042aap 生物膜中结合的环丙沙星的浓度。结果表明,分散素并没有增加结合的环丙沙星量,这表明分散素促进了环丙沙星进入细胞内靶标,从而导致抗生素敏感性增加。