共 39 条
Sequence-specific DNA solid-phase extraction in an on-chip monolith: Towards detection of antibiotic resistance genes
被引:9
作者:
Knob, Radim
[1
]
Nelson, Daniel B.
[2
]
Robison, Richard A.
[2
]
Woolley, Adam T.
[1
]
机构:
[1] Brigham Young Univ, Dept Chem & Biochem, Provo, UT 84602 USA
[2] Brigham Young Univ, Dept Microbiol & Mol Biol, Provo, UT 84602 USA
基金:
美国国家卫生研究院;
关键词:
Hybridization;
Microfluidics;
Monolith;
Sepsis;
HYBRIDIZATION;
CHROMATOGRAPHY;
PERFORMANCE;
PROTEIN;
BLOOD;
IDENTIFICATION;
PURIFICATION;
DIAGNOSTICS;
MONOVALENT;
SEPARATION;
D O I:
10.1016/j.chroma.2017.07.028
中图分类号:
Q5 [生物化学];
学科分类号:
071010 ;
081704 ;
摘要:
Antibiotic resistance of bacteria is a growing problem and presents a challenge for prompt treatment in patients with sepsis. Currently used methods rely on culturing or amplification; however, these steps are either time consuming or suffer from interference issues. A microfluidic device was made from black polypropylene, with a monolithic column modified with a capture oligonucleotide for sequence selective solid-phase extraction of a complementary target from a lysate sample. Porous properties of the monolith allow flow and hybridization of a target complementary to the probe immobilized on the column surface. Good flow-through properties enable extraction of a 100 mu L sample and elution of target DNA in 12 min total time. Using a fluorescently labeled target oligonucleotide related to Verona Integron-Mediated Metallo-beta-lactamase it was possible to extract and detect a 1 pM sample with 83% recovery. Temperature-mediated elution by heating above the duplex melting point provides a clean extract without any agents that interfere with base pairing, allowing various labeling methods or further downstream processing of the eluent. Further integration of this extraction module with a system for isolation and lysis of bacteria from blood, as well as combining with single-molecule detection should allow rapid determination of antibiotic resistance. (C) 2017 Elsevier B.V. All rights reserved.
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页码:309 / 315
页数:7
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