Center for Bio-Modular Multi-Scale Systems, Louisiana State University, 8000 G.SRI Road, Bldg. 3100, Baton Rouge, Louisiana 70820-7403, USA.
Anal Chem. 2010 Apr 1;82(7):2844-9. doi: 10.1021/ac100323k.
Low abundant (<100 cells mL(-1)) E. coli O157:H7 cells were isolated and enriched from environmental water samples using a microfluidic chip. The poly(methylmethacrylate), PMMA, chip contained 8 devices, each equipped with 16 curvilinear high aspect ratio channels that were covalently decorated with polyclonal anti-O157 antibodies (pAb) and could search for rare cells through a pAb mediated process. The chip could process independently 8 different samples or one sample using 8 different parallel inputs to increase volume processing throughput. After cell enrichment, cells were released and enumerated using benchtop real-time quantitative polymerase chain reaction (PCR), targeting genes which effectively discriminated the O157:H7 serotype from other nonpathogenic bacteria. The recovery of target cells from water samples was determined to be approximately 72%, and the limit-of-detection was found to be 6 colony forming units (cfu) using the slt1 gene as a reporter. We subsequently performed analysis of lake and wastewater samples. The simplicity in manufacturing and ease of operation makes this device attractive for the selection of pathogenic species from a variety of water supplies suspected of containing bacterial pathogens at extremely low frequencies.
从环境水样中分离和富集丰度低(<100 个细胞 mL(-1)) 的大肠杆菌 O157:H7 细胞,使用微流控芯片。聚(甲基丙烯酸甲酯),PMMA 芯片包含 8 个设备,每个设备都配备了 16 个曲线状高宽比通道,这些通道通过共价键与多克隆抗-O157 抗体(pAb)结合,可以通过 pAb 介导的过程搜索稀有细胞。该芯片可以独立处理 8 个不同的样本,也可以使用 8 个不同的并行输入处理一个样本,以增加体积处理通量。细胞富集后,使用台式实时定量聚合酶链反应(PCR)释放和计数细胞,该反应针对基因进行,这些基因可以有效地将 O157:H7 血清型与其他非致病性细菌区分开来。从水样中回收目标细胞的回收率约为 72%,使用 slt1 基因作为报告基因,检测限为 6 个菌落形成单位(cfu)。随后我们对湖水和废水样本进行了分析。该设备制造简单,操作简便,对于从各种水源中选择极低频率存在细菌病原体的致病性物种具有吸引力。