Integrated microfluidic tmRNA purification and real-time NASBA device for molecular diagnostics

被引:113
作者
Dimov, Ivan K. [1 ,3 ]
Garcia-Cordero, Jose L. [1 ]
O'Grady, Justin [2 ]
Poulsen, Claus R. [1 ]
Viguier, Caroline [1 ]
Kent, Lorcan [1 ]
Daly, Paul [1 ]
Lincoln, Bryan [1 ]
Maher, Majella [2 ]
O'Kennedy, Richard [1 ]
Smith, Terry J. [2 ]
Ricco, Antonio J. [1 ]
Lee, Luke P. [1 ,4 ]
机构
[1] Dublin City Univ, Natl Ctr Sensor Res, Biomed Diagnost Inst, Dublin 9, Ireland
[2] Natl Univ Ireland Univ Coll Galway, Biomed Diagnost Inst, Galway, Ireland
[3] Univ Valparaiso, Dept Biomed Engn, Valparaiso, Chile
[4] Univ Calif Berkeley, Berkeley Sensor & Actuator Ctr, Dept Bioengn, Biomol Nanotechnol Ctr, Berkeley, CA 94720 USA
关键词
D O I
10.1039/b812515e
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
We demonstrate the first integrated microfluidic tmRNA purification and nucleic acid sequence-based amplification (NASBA) device incorporating real-time detection. The real-time amplification and detection step produces pathogen-specific response in < 3 min from the chip-purified RNA from 100 lysed bacteria. On-chip RNA purification uses a new silica bead immobilization method. On-chip amplification uses custom-designed high-selectivity primers and real-time detection uses molecular beacon fluorescent probe technology; both are integrated on-chip with NASBA. Present in all bacteria, tmRNA (10Sa RNA) includes organism-specific identification sequences, exhibits unusually high stability relative to mRNA, and has high copy number per organism; the latter two factors improve the limit of detection, accelerate time-to-positive response, and suit this approach ideally to the detection of small numbers of bacteria. Device efficacy was demonstrated by integrated on-chip purification, amplification, and real-time detection of 100 E. coli bacteria in 100 mu L of crude lysate in under 30 min for the entire process.
引用
收藏
页码:2071 / 2078
页数:8
相关论文
共 38 条
[1]   Microchip-based purification of DNA from biological samples [J].
Breadmore, MC ;
Wolfe, KA ;
Arcibal, IG ;
Leung, WK ;
Dickson, D ;
Giordano, BC ;
Power, ME ;
Ferrance, JP ;
Feldman, SH ;
Norris, PM ;
Landers, JP .
ANALYTICAL CHEMISTRY, 2003, 75 (08) :1880-1886
[2]   Real-time PCR detection of Listeria monocytogenes using an integrated microfluidics platform [J].
Cady, NC ;
Stelick, S ;
Kunnavakkam, MV ;
Batt, CA .
SENSORS AND ACTUATORS B-CHEMICAL, 2005, 107 (01) :332-341
[3]  
CHEN L, 2007, LAB CHIP
[4]   Total nucleic acid analysis integrated on microfluidic devices [J].
Chen, Lin ;
Manz, Andreas ;
Day, Philip J. R. .
LAB ON A CHIP, 2007, 7 (11) :1413-1423
[5]   Microfluidic chip for high efficiency DNA extraction [J].
Chung, YC ;
Jan, MS ;
Lin, YC ;
Lin, JH ;
Cheng, WC ;
Fan, CY .
LAB ON A CHIP, 2004, 4 (02) :141-147
[6]   NUCLEIC-ACID SEQUENCE-BASED AMPLIFICATION [J].
COMPTON, J .
NATURE, 1991, 350 (6313) :91-92
[7]   Improved method for rapid DNA extraction of mastitis pathogens directly from milk [J].
Cremonesi, P ;
Castiglioni, B ;
Malferrari, G ;
Biunno, I ;
Vimercati, C ;
Moroni, P ;
Morandi, S ;
Luzzana, M .
JOURNAL OF DAIRY SCIENCE, 2006, 89 (01) :163-169
[8]   Micro total analysis systems. Latest advancements and trends [J].
Dittrich, Petra S. ;
Tachikawa, Kaoru ;
Manz, Andreas .
ANALYTICAL CHEMISTRY, 2006, 78 (12) :3887-3907
[9]   A fully integrated microfluidic genetic analysis system with sample-in-answer-out capability [J].
Easley, Christopher J. ;
Karlinsey, James M. ;
Bienvenue, Joan M. ;
Legendre, Lindsay A. ;
Roper, Michael G. ;
Feldman, Sanford H. ;
Hughes, Molly A. ;
Hewlett, Erik L. ;
Merkel, Tod J. ;
Ferrance, Jerome P. ;
Landers, James P. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (51) :19272-19277
[10]  
Garcia-Cordero JL, 2008, ENCY MICROFLUIDICS N, P962, DOI DOI 10.1007/978-0-387-48998-8_