Kaushik Aniruddha M, Hsieh Kuangwen, Mach Kathleen E, Lewis Shawna, Puleo Christopher M, Carroll Karen C, Liao Joseph C, Wang Tza-Huei
Department of Mechanical Engineering Johns Hopkins University Baltimore MD 21218 USA.
Department of Urology Stanford University School of Medicine Stanford CA 94305 USA.
Adv Sci (Weinh). 2021 Feb 1;8(6):2003419. doi: 10.1002/advs.202003419. eCollection 2021 Mar.
Empiric broad-spectrum antimicrobial treatments of urinary tract infections (UTIs) have contributed to widespread antimicrobial resistance. Clinical adoption of evidence-based treatments necessitates rapid diagnostic methods for pathogen identification (ID) and antimicrobial susceptibility testing (AST) with minimal sample preparation. In response, a microfluidic droplet-based platform is developed for achieving both ID and AST from urine samples within 30 min. In this platform, fluorogenic hybridization probes are utilized to detect 16S rRNA from single bacterial cells encapsulated in picoliter droplets, enabling molecular identification of uropathogenic bacteria directly from urine in as little as 16 min. Moreover, in-droplet single-bacterial measurements of 16S rRNA provide a surrogate for AST, shortening the exposure time to 10 min for gentamicin and ciprofloxacin. A fully integrated device and screening workflow were developed to test urine specimens for one of seven unique diagnostic outcomes including the presence/absence of Gram-negative bacteria, molecular ID of the bacteriaas , an , or other organism, and assessment of bacterial susceptibility to ciprofloxacin. In a 50-specimen clinical comparison study, the platform demonstrates excellent performance compared to clinical standard methods (areas-under-curves, AUCs >0.95), within a small fraction of the turnaround time, highlighting its clinical utility.
尿路感染(UTIs)的经验性广谱抗菌治疗导致了广泛的抗菌药物耐药性。基于证据的治疗方法在临床上的应用需要快速的诊断方法来进行病原体鉴定(ID)和抗菌药物敏感性测试(AST),且样本制备要求最低。作为回应,开发了一种基于微流控液滴的平台,可在30分钟内从尿液样本中同时实现ID和AST。在这个平台上,荧光杂交探针被用于检测皮升液滴中封装的单个细菌细胞的16S rRNA,从而能够在短短16分钟内直接从尿液中对尿路致病性细菌进行分子鉴定。此外,对16S rRNA进行液滴内单细菌测量可作为AST的替代方法,将庆大霉素和环丙沙星的暴露时间缩短至10分钟。开发了一种完全集成的设备和筛查工作流程,以针对七种独特诊断结果之一对尿液标本进行检测,包括革兰氏阴性菌的有无、细菌的分子鉴定、其他生物体的鉴定以及细菌对环丙沙星的敏感性评估。在一项包含50个样本的临床比较研究中,该平台与临床标准方法相比表现出色(曲线下面积,AUCs>0.95),且周转时间仅为一小部分,突出了其临床实用性。