Zhang Huilin, Huang Fengchun, Cai Gaozhe, Li Yuntao, Lin Jianhan
Key Laboratory of Agricultural Information Acquisition Technology, Ministry of Agriculture, China Agricultural University, Beijing 100083, China.
State Key Lab of Integrated Optoelectronics, Institute of Semiconductors, Chinese Academy of Science, Beijing 100083, China.
J Dairy Sci. 2018 Nov;101(11):9736-9746. doi: 10.3168/jds.2018-14730. Epub 2018 Sep 13.
In this study, a rapid and sensitive method for detection of Escherichia coli O157:H7 using the coaxial channel-based DNA extraction and the microfluidic PCR was proposed and verified. The magnetic silica beads were first pumped into the coaxial channel, which was captured in the coaxial channel more uniformly by applying the multiring high-gradient magnetic field. After the E. coli O157:H7 cells were lysed with the lysis buffer to release the DNA, the improved coaxial channel was used to efficiently extract the DNA, followed by washing with ethanol to remove the residual proteins and eluting with a small volume of deionized water to obtain the purified and concentrated DNA. Finally, the obtained DNA was amplified and determined using the microfluidic PCR. This proposed bacteria detection method was able to detect E. coli O157:H7 as low as 12 cfu/mL when the large volume (10 mL) of bacterial sample was used, and the recovery of E. coli O157:H7 in the spiked milk samples ranged from 97.4 to 100.6%. This proposed bacteria detection method has shown great potential to detect lower concentration of E. coli O157:H7 from larger volumes of sample.
在本研究中,提出并验证了一种基于同轴通道DNA提取和微流控PCR的快速灵敏检测大肠杆菌O157:H7的方法。首先将磁性硅胶珠泵入同轴通道,通过施加多环高梯度磁场使其更均匀地捕获在同轴通道中。在用裂解缓冲液裂解大肠杆菌O157:H7细胞以释放DNA后,使用改进的同轴通道高效提取DNA,然后用乙醇洗涤以去除残留蛋白质,并用少量去离子水洗脱以获得纯化和浓缩的DNA。最后,使用微流控PCR对获得的DNA进行扩增和测定。当使用大量(10 mL)细菌样品时,这种提出的细菌检测方法能够检测低至12 cfu/mL的大肠杆菌O157:H7,加标牛奶样品中大肠杆菌O157:H7的回收率在97.4%至100.6%之间。这种提出的细菌检测方法在从大量样品中检测较低浓度的大肠杆菌O157:H7方面显示出巨大潜力。