Multiplexed Bead-Based Mesofluidic System for Detection of Food-Borne Pathogenic Bacteria

被引:29
作者
Jin, Sheng-Quan [1 ]
Yin, Bin-Cheng [1 ]
Ye, Bang-Ce [1 ]
机构
[1] E China Univ Sci & Technol, Lab Biosyst & Microanal, State Key Lab Bioreactor Engn, Shanghai 200237, Peoples R China
关键词
POLYMERASE-CHAIN-REACTION; REAL-TIME PCR; CEREUS DIARRHEAL ENTEROTOXIN; ESCHERICHIA-COLI O157-H7; DNA HYBRIDIZATION; LISTERIA-MONOCYTOGENES; RAPID DETECTION; MICROARRAYS; ASSAY; IDENTIFICATION;
D O I
10.1128/AEM.00854-09
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
In the present study, a simple and rapid multiplexed bead-based mesofluidic system (BMS) was developed for simultaneous detection of food-borne pathogenic bacteria, including Staphylococcus aureus, Vibrio parahaemolyticus, Listeria monocytogenes, Salmonella, Enterobacter sakazakii, Shigella, Escherichia coli O157:H7, and Campylobacter jejuni. This system is based on utilization of isothiocyanate-modified microbeads that are 250 mu m in diameter, which were immobilized with specific amino-modified oligonucleotide probes and placed in polydimethylsiloxane microchannels. PCR products from the pathogens studied were pumped into microchannels to hybridize with the oligonucleotide-modified beads, and hybridization signals were detected using a conventional microarray scanner. The short sequences of nucleic acids (21 bases) and PCR products characteristic of bacterial pathogens could be detected at concentrations of 1 pM and 10 nM, respectively. The detection procedure could be performed in less than 30 min with high sensitivity and specificity. The assay was simple and fast, and the limits of quantification were in the range from 500 to 6,000 CFU/ml for the bacterial species studied. The feasibility of identification of food-borne bacteria was investigated with samples contaminated with bacteria, including milk, egg, and meat samples. The results demonstrated that the BMS method can be used for effective detection of multiple pathogens in different foodstuffs.
引用
收藏
页码:6647 / 6654
页数:8
相关论文
共 44 条
  • [21] Dendrimeric coating of glass slides for sensitive DNA microarrays analysis -: art. no. e88
    Le Berre, V
    Trévisiol, E
    Dagkessamanskaia, A
    Sokol, S
    Caminade, AM
    Majoral, JP
    Meunier, B
    François, J
    [J]. NUCLEIC ACIDS RESEARCH, 2003, 31 (16)
  • [22] Development of a novel hand-held immunoassay for the detection of enterohemorrhagic Escherichia coli O157:H7
    Lin, FYH
    Sherman, PM
    Li, DQ
    [J]. BIOMEDICAL MICRODEVICES, 2004, 6 (02) : 125 - 130
  • [23] PCR and oligonucleotide array for detection of Enterobacter sakazakii in infant formula
    Liu, Y
    Gao, QL
    Zhang, X
    Hou, YM
    Yang, JL
    Huang, XT
    [J]. MOLECULAR AND CELLULAR PROBES, 2006, 20 (01) : 11 - 17
  • [24] LU CY, 2009, CHIN J BIOTECHNOL, V25, P554
  • [25] Carbon and gold electrodes as electrochemical transducers for DNA hybridisation sensors
    Lucarelli, F
    Marrazza, G
    Turner, APF
    Mascini, M
    [J]. BIOSENSORS & BIOELECTRONICS, 2004, 19 (06) : 515 - 530
  • [26] Food-related illness and death in the United States
    Mead, PS
    Slutsker, L
    Dietz, V
    McCaig, LF
    Bresee, JS
    Shapiro, C
    Griffin, PM
    Tauxe, RV
    [J]. EMERGING INFECTIOUS DISEASES, 1999, 5 (05) : 607 - 625
  • [27] Detection of pathogenic Vibrio spp. in shellfish by using multiplex PCR and DNA microarrays
    Panicker, G
    Call, DR
    Krug, MJ
    Bej, AK
    [J]. APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2004, 70 (12) : 7436 - 7444
  • [28] The effect of surface probe density on DNA hybridization
    Peterson, AW
    Heaton, RJ
    Georgiadis, RM
    [J]. NUCLEIC ACIDS RESEARCH, 2001, 29 (24) : 5163 - 5168
  • [29] High-throughput SPR sensor for food safety
    Piliarik, Marek
    Parova, Lucie
    Homola, Jiri
    [J]. BIOSENSORS & BIOELECTRONICS, 2009, 24 (05) : 1399 - 1404
  • [30] Radke V, 2006, J ENVIRON HEALTH, V69, P34