Highly Selective, Sensitive and Rapid Detection of Escherichia coli O157: H7 Using Duplex PCR and Magnetic Nanoparticle-Based Chemiluminescence Assay

被引:90
|
作者
He, Lei [1 ]
Yang, Haowen [1 ,2 ]
Xiao, Pengfeng [1 ]
Singh, Ravina [6 ]
He, Nongyue [1 ,4 ]
Liu, Bin [3 ]
Li, Zhiyang [5 ]
机构
[1] Southeast Univ, Sch Biol & Med Engn, State Key Lab Bioelect, Nanjing 210096, Jiangsu, Peoples R China
[2] ETH, Dept Chem & Appl Biosci, Inst Chem & Bioengn, CH-8093 Zurich, Switzerland
[3] Nanjing Med Univ, Sch Basic Med Sci, Dept Biomed Engn, Nanjing 211166, Jiangsu, Peoples R China
[4] Hunan Univ Technol, Hunan Key Lab Biomed Nanomat & Devices, Econ Forest Cultivat & Utilizat Collaborat Innova, Zhuzhou 412007, Peoples R China
[5] Nanjing Univ Med Sch, Affiliated Drum Tower Hosp, Dept Clin Lab, Nanjing 210008, Jiangsu, Peoples R China
[6] Univ Calif Berkeley, Berkeley, CA 94720 USA
关键词
Magnetic Nanoparticles; Chemiluminescence; E. coli O157: H7; Duplex PCR; rfbE; fliC; POLYMERASE-CHAIN-REACTION; FACILE SYNTHESIS; GOLD NANORODS; DAIRY-PRODUCTS; III SECRETION; FOOD ANIMALS; APTAMER; SYSTEM; AMPLIFICATION; EFFICIENT;
D O I
10.1166/jbn.2017.2422
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
A novel strategy based on duplex PCR and chemiluminescence (CL) was developed in this study to identify Escherichia coli (E. coli) O157: H7 serotype. The antigen epitopes O157 gene (rfbE) and flagella antigen H7 gene (fliC) were simultaneously amplified and labelled with biotin through duplex PCR. The biotinylated rfbE and fliC amplicons were captured to the surface of oligonucleotide probe-modified magnetic nanoparticles (MNPs) successively. After being conjugated with alkaline phosphatase-labelled streptavidin (ALP-STA), the substrate 3-(2'-Spiroadamantane)-4-methoxy-4( 3''-phosphoryloxy)-phenyl-1,2-dioxetane (AMPPD) was mixed with the magnetic complexes and CL signals were generated immediately. The stable CL intensity reflected the amount of rfbE and fliC genes, which confirmed the presence of E. coli O157: H7. The detection limit was 10 pM under optimized conditions. The detection results from food samples indicated that this approach is reliable and repeatable, thus holding great potential for rapid, highly selective and sensitive food inspection.
引用
收藏
页码:1243 / 1252
页数:10
相关论文
共 50 条
  • [31] Escherichia coli O157:H7
    Hartigan, PJ
    IRISH VETERINARY JOURNAL, 1997, 50 (02) : 91 - +
  • [32] Escherichia coli O157:H7
    Riemann, HP
    Cliver, DO
    VETERINARY CLINICS OF NORTH AMERICA-FOOD ANIMAL PRACTICE, 1998, 14 (01) : 41 - +
  • [33] Escherichia coli O157:H7
    Mead, PS
    Griffin, PM
    LANCET, 1998, 352 (9135): : 1207 - 1212
  • [34] A remarkable sensitivity enhancement in a gold nanoparticle-based lateral flow immunoassay for the detection of Escherichia coli O157:H7
    Cui, Xi
    Huang, Youju
    Wang, Jingyun
    Zhang, Lei
    Rong, Yun
    Lai, Weihua
    Chen, Tao
    RSC ADVANCES, 2015, 5 (56) : 45092 - 45097
  • [35] Escherichia coli O157:H7
    Tarr, PI
    Neill, MA
    GASTROENTEROLOGY CLINICS OF NORTH AMERICA, 2001, 30 (03) : 735 - +
  • [36] Escherichia coli O157:H7
    OLoughin, E
    LANCET, 1997, 349 (9064): : 1553 - 1553
  • [37] Lateral flow assay strip for detection of Escherichia coli O157:H7
    Suria, M. S.
    Afendy, Mohd A. T.
    Azlina, Noor M.
    Zamri, I
    INTERNATIONAL FOOD RESEARCH JOURNAL, 2015, 22 (06): : 2587 - 2593
  • [38] Development of a quantitative competitive PCR assay for detection and quantification of Escherichia coli O157:H7 cells
    Li, WL
    Drake, MA
    APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2001, 67 (07) : 3291 - 3294
  • [39] Sensitive detection of Escherichia coli O157:H7 by conventional plating techniques
    Jordan, KN
    Maher, MM
    JOURNAL OF FOOD PROTECTION, 2006, 69 (03) : 689 - 692
  • [40] Development of a real time PCR assay for detecting H7 in Escherichia coli O157
    Chui, L.
    Hinck, T.
    Wang, G.
    Tabor, H.
    Louie, M.
    INTERNATIONAL JOURNAL OF ANTIMICROBIAL AGENTS, 2009, 34 : S3 - S3