Liao Joseph C, Mastali Mitra, Gau Vincent, Suchard Marc A, Møller Annette K, Bruckner David A, Babbitt Jane T, Li Yang, Gornbein Jeffrey, Landaw Elliot M, McCabe Edward R B, Churchill Bernard M, Haake David A
Division of Infectious Diseases, 111F, VA Greater LA Healthcare, Los Angeles, CA 90073, USA.
J Clin Microbiol. 2006 Feb;44(2):561-70. doi: 10.1128/JCM.44.2.561-570.2006.
We describe the first species-specific detection of bacterial pathogens in human clinical fluid samples using a microfabricated electrochemical sensor array. Each of the 16 sensors in the array consisted of three single-layer gold electrodes-working, reference, and auxiliary. Each of the working electrodes contained one representative from a library of capture probes, each specific for a clinically relevant bacterial urinary pathogen. The library included probes for Escherichia coli, Proteus mirabilis, Pseudomonas aeruginosa, Enterocococcus spp., and the Klebsiella-Enterobacter group. A bacterial 16S rRNA target derived from single-step bacterial lysis was hybridized both to the biotin-modified capture probe on the sensor surface and to a second, fluorescein-modified detector probe. Detection of the target-probe hybrids was achieved through binding of a horseradish peroxidase (HRP)-conjugated anti-fluorescein antibody to the detector probe. Amperometric measurement of the catalyzed HRP reaction was obtained at a fixed potential of -200 mV between the working and reference electrodes. Species-specific detection of as few as 2,600 uropathogenic bacteria in culture, inoculated urine, and clinical urine samples was achieved within 45 min from the beginning of sample processing. In a feasibility study of this amperometric detection system using blinded clinical urine specimens, the sensor array had 100% sensitivity for direct detection of gram-negative bacteria without nucleic acid purification or amplification. Identification was demonstrated for 98% of gram-negative bacteria for which species-specific probes were available. When combined with a microfluidics-based sample preparation module, the integrated system could serve as a point-of-care device for rapid diagnosis of urinary tract infections.
我们描述了首次使用微制造电化学传感器阵列对人类临床体液样本中的细菌病原体进行物种特异性检测。该阵列中的16个传感器每个都由三个单层金电极组成——工作电极、参比电极和辅助电极。每个工作电极都包含来自捕获探针库的一个代表,每个探针都对临床上相关的细菌性尿路病原体具有特异性。该库包括针对大肠杆菌、奇异变形杆菌、铜绿假单胞菌、肠球菌属以及克雷伯菌 - 肠杆菌组的探针。源自单步细菌裂解的细菌16S rRNA靶标与传感器表面的生物素修饰捕获探针以及第二个荧光素修饰检测探针杂交。通过辣根过氧化物酶(HRP)偶联的抗荧光素抗体与检测探针结合来实现对靶标 - 探针杂交体的检测。在工作电极和参比电极之间 -200 mV的固定电位下进行催化的HRP反应的安培测量。从样品处理开始后的45分钟内,实现了对培养物、接种尿液和临床尿液样本中低至2600个尿路致病性细菌的物种特异性检测。在使用盲法临床尿液样本对该安培检测系统进行的可行性研究中,该传感器阵列对革兰氏阴性菌的直接检测具有100%的灵敏度,无需核酸纯化或扩增。对于有物种特异性探针的革兰氏阴性菌,98%实现了鉴定。当与基于微流体的样品制备模块结合时,该集成系统可作为用于快速诊断尿路感染的即时检测设备。