Department of Chemistry, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.
Lab Chip. 2013 Apr 7;13(7):1325-32. doi: 10.1039/c3lc40961a.
A microfluidic chip integrating DNA extraction, amplification, and detection for the identification of bacteria in saliva is described. The chip design integrated a monolithic aluminum oxide membrane (AOM) for DNA extraction with seven parallel reaction wells for real-time polymerase chain reaction (rtPCR) amplification of the extracted DNA. Samples were first heated to lyse target organisms and then added to the chip and filtered through the nanoporous AOM to extract the DNA. PCR reagents were added to each of the wells and the chip was thermocycled. Identification of Streptococcus mutans in a saliva sample is demonstrated along with the detection of 300 fg (100-125 copies) of both methicillin-susceptible Staphylococcus aureus (MSSA) and methicillin-resistant S. aureus (MRSA) genomic DNA (gDNA) spiked into a saliva sample. Multiple target species and strains of bacteria can be simultaneously identified in the same sample by varying the primers and probes used in each of the seven reaction wells. In initial tests, as little as 30 fg (8-12 copies) of MSSA gDNA in buffer has been successfully amplified and detected with this device.
介绍了一种用于唾液中细菌鉴定的集成了 DNA 提取、扩增和检测的微流控芯片。该芯片设计集成了用于 DNA 提取的单片氧化铝膜 (AOM) 和 7 个平行反应池,用于提取的 DNA 的实时聚合酶链反应 (rtPCR) 扩增。样品首先加热以裂解目标生物,然后添加到芯片中,并通过纳米多孔 AOM 过滤以提取 DNA。将 PCR 试剂添加到每个孔中,并对芯片进行热循环。该芯片成功地对唾液样本中的变异链球菌进行了鉴定,同时检测到了 300 fg(100-125 拷贝)经唾液样本稀释的耐甲氧西林金黄色葡萄球菌 (MSSA) 和耐甲氧西林金黄色葡萄球菌 (MRSA) 基因组 DNA (gDNA)。通过在七个反应池中使用不同的引物和探针,可以同时对同一样本中的多种目标细菌种类和菌株进行鉴定。在初步测试中,该设备已成功扩增和检测到缓冲液中低至 30 fg(8-12 拷贝)的 MSSA gDNA。