A microfluidic chip integrating DNA extraction and real-time PCR for the detection of bacteria in saliva

被引:121
|
作者
Oblath, Emily A. [1 ]
Henley, W. Hampton [1 ]
Alarie, Jean Pierre [1 ]
Ramsey, J. Michael [1 ]
机构
[1] Univ N Carolina, Dept Chem, Chapel Hill, NC 27599 USA
基金
美国国家卫生研究院;
关键词
NUCLEIC-ACID AMPLIFICATION; SAMPLE PREPARATION; SYSTEM; IDENTIFICATION; DIAGNOSTICS; INHIBITION; DEVICES; BIOCHIP; ARRAY;
D O I
10.1039/c3lc40961a
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:1325 / 1332
页数:8
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