An integrated microfluidic system for diagnosis of the resistance of Helicobacter pylori to quinolone-based antibiotics

被引:23
作者
Chao, Chih-Yu [1 ]
Wang, Chih-Hung [2 ]
Che, Yu-Jui [2 ]
Kao, Cheng-Yen [3 ]
Wu, Jiunn-Jong [3 ,4 ]
Lee, Gwo-Bin [1 ,2 ]
机构
[1] Natl Tsing Hua Univ, Inst Biomed Engn, Hsinchu, Taiwan
[2] Natl Tsing Hua Univ, Dept Power Mech Engn, Hsinchu 30013, Taiwan
[3] Natl Cheng Kung Univ, Dept Med Lab Sci & Biotechnol, Tainan 701, Taiwan
[4] Natl Yang Ming Univ, Sch Biomed Sci & Engn, Dept Biotechnol & Lab Sci Med, Taipei 112, Taiwan
关键词
Microfluidic; H; pylori; SNP-PCR; Optical detection; Antibiotic resistance detection; NUCLEIC-ACID AMPLIFICATION; RIBOSOMAL-RNA GENE; POINT MUTATIONS; RAPID DETECTION; MAGNETIC BEADS; DNA; PCR; SUSCEPTIBILITY; INFECTION; CLARITHROMYCIN;
D O I
10.1016/j.bios.2015.11.046
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Helicobacter pylori (H. pylori) is a species of bacteria that can colonize the human stomach mucosa. It is closely associated with gastric diseases such as ulcer and inflammation. Recently, some H. pylori strains were found to express resistance to a family of antibiotics known as quinolones due to single-point mutations. Although traditional polymerase chain reaction (PCR) and molecular diagnostic-based approaches can be used to determine the presence and abundance of antibiotic-resistant H. pylori strains, such processes are relatively expensive, labor-intensive, and require bulky and costly equipment. This study therefore reports an advanced diagnostic assay performed on an integrated microfluidic system for rapid detection of antibiotic resistance in H. pylori. The assay features three components: (1) nucleic acid extraction by specific probe-conjugated magnetic beads, (2) amplification of the target deoxyribonucleic acid (DNA) fragments by using single-nucleotide-polymorphism polymerase chain reaction (SNP-PCR), and (3) optical detection of the PCR products. The device integrates several microfluidic components including micro-pumps, normally-closed micro-valves, and reaction chambers such that the entire diagnostic assay can be automatically executed on a single microfluidic system within one hour with detection limits of 10(0), 10(2), and 10(2) bacterial cells for H. pylori detection and two different SNP sites strains. Three PCR-based assays for determining presence of H. pylori infection and two DNA single-point mutation assays aimed at determining whether the infected strains were resistant to quinolone can be performed simultaneously on a single chip, suggesting that this microfluidic system could be a promising tool for rapid diagnosis of the presence of antibiotic-resistant H. pylori strains. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:281 / 289
页数:9
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