| Literature DB >> 24720991 |
Xiran Jiang1, Ning Shao2, Wenwen Jing3, Shengce Tao2, Sixiu Liu1, Guodong Sui4.
Abstract
Rapid identification of clinical pathogens is the initial and essential step for antimicrobial therapy. Herein, we successfully developed a microfluidic device which combines high-throughput continuous-flow PCR and DNA hybridization for the detection of various bacterial pathogens. Universal primers were designed based on the conserved regions of bacterial 16S ribosomal DNA (16S rDNA), and specific probes were designed from a variable region of 16S rDNA within the amplicon sequences. In the chip operation, after the continuous flow PCR was achieved in the first microfluidic chip, the product was directly introduced into a hybridization chip integrated with microarray containing the immobilized DNA probes. The target-probe hybridization was completed within 1h at 55 °C, and fluorescence signals were obtained as the readout. The presented device is simple, versatile and with less sample consumption compared with traditional instruments. It can perform high-throughput bacteria detections continuously in a single assay, which makes it a promising platform for clinical bacteria identifications.Entities:
Keywords: 16S rDNA; Continuous-flow PCR; Hybridization
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Year: 2014 PMID: 24720991 DOI: 10.1016/j.talanta.2014.01.053
Source DB: PubMed Journal: Talanta ISSN: 0039-9140 Impact factor: 6.057