iso-μmGene: an isothermal amplification-based portable microfluidic system for simple, reliable and flexibly multiplexed genetic identification and quantification

被引:6
|
作者
Zhong, Runtao [1 ]
Liu, Shilin [1 ]
Zhang, Guohao [2 ]
Wang, Mengyu [1 ]
Sun, Yeqing [1 ]
机构
[1] Dalian Maritime Univ, Inst Environm Syst Biol, 1 Linghai Rd, Dalian 116026, Peoples R China
[2] Beijing Baicare Biotechnol Co Ltd, Zhongguancun Life Sci Pk, Beijing 102206, Peoples R China
关键词
RAPID DETECTION; EDWARDSIELLA-TARDA; CHIP; LAMP; POINT; ASSAY; PLATFORMS;
D O I
10.1039/d0an00560f
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Simple, reliable and flexibly multiplexed genetic identification and quantification of microbial pathogens is in urgent need for early disease diagnosis and timely treatment. This study presented an isothermal amplification-based portable microfluidic system (iso-mu mGene) with features of multi-well chips for convenient filling and reliable sealing, flexible detection throughput, and a stand-alone and well-performing point of care (POC) genetic testing device. Using disposable chips with two kinds of reaction wells (eighteen and ten wells) and a device prototype with independent four chip holders, theiso-mu mGeneenables on-demand analysis of different target genes in one sample per chip and one to four samples (chips) per run, requiring only a single pipetting step for dispensing per chip with dehydrated primers. To completely seal the loop-mediated isothermal amplification (LAMP) reaction system to minimize the risk of amplicon escape, a dedicated plastic shell is used to assemble the array-type chip and reliably close its openings. Meanwhile, to enhance the precision for flexibly multiplexed detection and decrease the size and cost of the device, we designed a thermoelectric cooler (TEC)-based temperature-control module including two separate units and a CCD-based fluorescence imaging module containing a linear translation stage for real-time LAMP assay. This work demonstrated applications for the parallel detection of 2-2000 CFU (colony forming units) per reaction well with good intra- and inter-chip reproducibility using the crude lysates of two aquaculture pathogensEdwardsiella tardaandVibrio harveyi. Overall, theiso-mu mGenepresented here possesses both a sophisticated instrument's functionality and performance and POC device's portability and cost.
引用
收藏
页码:4627 / 4636
页数:10
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