Cell lysis and DNA extraction of gram-positive and gram-negative bacteria from whole blood in a disposable microfluidic chip

被引:145
作者
Mahalanabis, Madhumita [1 ]
Al-Muayad, Hussam [1 ]
Kulinski, M. Dominika
Altman, Dave
Klapperich, Catherine M. [1 ]
机构
[1] Boston Univ, Dept Biomed Engn, Boston, MA 02215 USA
关键词
POLYMERASE-CHAIN-REACTION; MECHANICAL-PROPERTIES; RAPID DIAGNOSIS; SEPSIS; AMPLIFICATION; EPIDEMIOLOGY; DISRUPTION; ASSAY; PEPTIDOGLYCAN; PURIFICATION;
D O I
10.1039/b905065p
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Sepsis caused by gram positive and gram negative bacteria is the leading cause of death in noncoronary ICUs and the tenth leading cause of death in the United States. We have developed a microfluidic sample preparation platform for rapid on-chip detection of infectious organisms for point-of-care diagnostics. The microfluidic chips are made of a robust thermoplastic and can be easily multiplexed for high throughput applications. Bacteria are lysed on-chip via hybrid chemical/mechanical method. Once lysed, the bacterial DNA is isolated using a microscale silica bead/polymer composite solid-phase-extraction (SPE) column. Lysis was confirmed using off-chip real time PCR. We isolated and detected both gram-negative (Escherichia coli) and gram-positive (Bacillus subtilis and Enterococcus faecalis) bacterial genomic DNA from microliter scale spiked whole human blood samples. The system performs better for gram-negative bacteria than it does for gram-positive bacteria, with limits of detection at 10(2) CFU/ml and 10(3)-10(4) CFU/ml, respectively. Total extraction times are less than one hour and can be further decreased by altering the channel geometry and pumping configuration.
引用
收藏
页码:2811 / 2817
页数:7
相关论文
共 36 条
[1]   Epidemiology of severe sepsis in the United States: Analysis of incidence, outcome, and associated costs of care [J].
Angus, DC ;
Linde-Zwirble, WT ;
Lidicker, J ;
Clermont, G ;
Carcillo, J ;
Pinsky, MR .
CRITICAL CARE MEDICINE, 2001, 29 (07) :1303-1310
[2]   Efficacy and safety of recombinant human activated protein C for severe sepsis. [J].
Bernard, GR ;
Vincent, JL ;
Laterre, P ;
LaRosa, SP ;
Dhainaut, JF ;
Lopez-Rodriguez, A ;
Steingrub, JS ;
Garber, GE ;
Helterbrand, JD ;
Ely, EW ;
Fisher, CJ .
NEW ENGLAND JOURNAL OF MEDICINE, 2001, 344 (10) :699-709
[3]   Thermoplastic microfluidic device for on-chip purification of nucleic acids for disposable diagnostics [J].
Bhattacharyya, A ;
Klapperich, CM .
ANALYTICAL CHEMISTRY, 2006, 78 (03) :788-792
[4]  
BHATTACHARYYA A, 2008, ENCY MICRO NANOFLUID, P2226
[5]   Microfluidics-based extraction of viral RNA from infected mammalian cells for disposable molecular diagnostics [J].
Bhattacharyya, Arpita ;
Klapperich, Catherine A. .
SENSORS AND ACTUATORS B-CHEMICAL, 2008, 129 (02) :693-698
[6]   Mechanical and chemical analysis of plasma and ultraviolet-ozone surface treatments for thermal bonding of polymeric microfluidic devices [J].
Bhattacharyya, Arpita ;
Klapperich, Catherine M. .
LAB ON A CHIP, 2007, 7 (07) :876-882
[7]   RAPID AND SIMPLE METHOD FOR PURIFICATION OF NUCLEIC-ACIDS [J].
BOOM, R ;
SOL, CJA ;
SALIMANS, MMM ;
JANSEN, CL ;
WERTHEIMVANDILLEN, PME ;
VANDERNOORDAA, J .
JOURNAL OF CLINICAL MICROBIOLOGY, 1990, 28 (03) :495-503
[8]   Bacterial cell shape [J].
Cabeen, MT ;
Jacobs-Wagner, C .
NATURE REVIEWS MICROBIOLOGY, 2005, 3 (08) :601-610
[9]  
CHEN LH, 2009, CLIN PEDIAT PHILA
[10]   Reagentless mechanical cell lysis by nanoscale barbs in microchannels for sample preparation [J].
Di Carlo, D ;
Jeong, KH ;
Lee, LP .
LAB ON A CHIP, 2003, 3 (04) :287-291