Chemical and Biological Engineering Department, Colorado School of Mines, Golden, CO, USA.
Analyst. 2020 Jun 7;145(11):3996-4003. doi: 10.1039/d0an00479k. Epub 2020 Apr 28.
In clinical environments, many serious antibiotic-resistant infections are caused by biofilm-forming species. This presents issues when attempting to determine antimicrobial dosing as traditional antibiotic susceptibility tests (ASTs) are typically designed around planktonic bacteria and thus offer information that is not relevant to the biofilm phenotype present in the patient. Even the popular Calgary biofilm device may provide inaccurate minimum biofilm inhibitory concentrations (MBICs) and can be time- and material-intensive. In this work, we present a method utilizing oxygen-sensitive nanosensor technology to monitor the oxygen consumption dynamics of living biofilms as they are exposed to antibiotics. We incorporated our nanosensors into biofilms grown from P. aeruginosa strains of varying sensitivity to traditional classes of antibiotics. Through measuring nanosensor response under antibiotic administration we determined the concentrations able to cease biofilm metabolism. This method provides information on the MBIC as well as kinetic response information in a manner that requires fewer materials and is more reflective of biofilm behavior than a traditional AST.
在临床环境中,许多由生物膜形成物种引起的严重抗生素耐药感染。当试图确定抗菌药物剂量时,这会带来问题,因为传统的抗生素药敏试验(AST)通常是围绕浮游细菌设计的,因此提供的信息与患者体内存在的生物膜表型不相关。即使是流行的卡尔加里生物膜装置也可能提供不准确的最小生物膜抑制浓度(MBIC),并且可能耗时且材料密集。在这项工作中,我们提出了一种利用氧敏感纳米传感器技术来监测抗生素暴露下活生物膜的氧消耗动力学的方法。我们将纳米传感器整合到来自不同敏感传统抗生素类别的铜绿假单胞菌菌株中生长的生物膜中。通过在抗生素给药下测量纳米传感器的响应,我们确定了能够停止生物膜代谢的浓度。该方法以比传统 AST 更能反映生物膜行为的方式提供了关于 MBIC 以及动力学响应信息,所需材料更少。