Polymyxin-based enzyme-linked immunosorbent assay for the detection of Escherichia coli O111 and O26

被引:11
作者
Blais, BW [1 ]
Bosley, J [1 ]
Martinez-Perez, A [1 ]
Popela, M [1 ]
机构
[1] Canadian Food Inspect Agcy, Ottawa Lab Carling, Ottawa, ON K1A 0C6, Canada
关键词
polymyxin-ELISA; Escherichia coli O111; O26; lipopolysaccharide;
D O I
10.1016/j.mimet.2005.09.004
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Polymyxin-based enzyme-linked inununosorbent assay (polymyxin-ELISA) systems were developed for the detection of Escherichia coli O111 and O26 in ground beef after enrichment. Polymyxin immobilized in the wells of a microtiter plate served as a high affinity adsorbent for lipopolysaccharide (LPS) antigens, which were detected immunoenzymatically using commercially available anti-E. coli O111 or anti-E. coli O26 antisera. The polymyxin-ELISA sensitively detected E. coli strains bearing the O111 and O26 LPS antigens, discriminating between these target strains and a panel of various non-target Gram negative and Gram positive bacteria. The detection of E. coli O111 and O26 strains inoculated into ground beef was achieved after enrichment in either modified trypticase soy broth (TSB) with novobiocin, or the serotype-specific medium TSB supplemented with cefixime and vancomycin (E. coli O111), and the same medium containing potassium tellurite (E. coli O26). The polymyxin-ELISA shows promise as a rapid, simple and inexpensive screening tool for E. coli O111 and O26 in enrichment cultures of ground beef (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:468 / 475
页数:8
相关论文
共 16 条
[1]   Seasonal prevalence of Shiga toxin-producing Escherichia coli, including O157:H7 and non-O157 serotypes, and Salmonella in commercial beef processing plants [J].
Barkocy-Gallagher, GA ;
Arthur, TM ;
Rivera-Betancourt, M ;
Nou, XW ;
Shackelford, SD ;
Wheeler, TL ;
Koohmaraie, M .
JOURNAL OF FOOD PROTECTION, 2003, 66 (11) :1978-1986
[2]   Comparison of fluorogenic and chromogenic assay systems in the detection of Escherichia coli O157 by a novel polymyxin-based ELISA [J].
Blais, BW ;
Leggate, J ;
Bosley, J ;
Martinez-Perez, A .
LETTERS IN APPLIED MICROBIOLOGY, 2004, 39 (06) :516-522
[3]   Optimization of enrichment and plating procedures for the recovery of Escherichia coli O111 and O26 from minced beef [J].
Catarame, TMG ;
O'Hanlon, KA ;
Duffy, G ;
Sheridan, JJ ;
Blair, IS ;
McDowell, DA .
JOURNAL OF APPLIED MICROBIOLOGY, 2003, 95 (05) :949-957
[4]   A PCR specific for Escherichia coli O157 based on the rfb locus encoding O157 lipopolysaccharide [J].
Desmarchelier, PM ;
Bilge, SS ;
Fegan, N ;
Mills, L ;
Vary, JC ;
Tarr, PI .
JOURNAL OF CLINICAL MICROBIOLOGY, 1998, 36 (06) :1801-1804
[5]   ESCHERICHIA-COLI O157 - H7 AND ITS SIGNIFICANCE IN FOODS [J].
DOYLE, MP .
INTERNATIONAL JOURNAL OF FOOD MICROBIOLOGY, 1991, 12 (04) :289-302
[6]  
Hara-Kudo Y, 2000, LETT APPL MICROBIOL, V30, P151, DOI 10.1046/j.1472-765X.2000.00686.x
[7]   Invited review:: Prevalence of Shiga toxin-producing Escherichia coli in dairy cattle and their products [J].
Hussein, HS ;
Sakuma, T .
JOURNAL OF DAIRY SCIENCE, 2005, 88 (02) :450-465
[8]   Detection of Escherichia coli serogroups O26, O103, O111 and O145 from bovine faeces using immunomagnetic separation and PCR/DNA probe techniques [J].
Jenkins, C ;
Pearce, MC ;
Smith, AW ;
Knight, HI ;
Shaw, DJ ;
Cheasty, T ;
Foster, G ;
Gunn, GJ ;
Dougan, G ;
Smith, HR ;
Frankel, G .
LETTERS IN APPLIED MICROBIOLOGY, 2003, 37 (03) :207-212
[9]   Epidemiology and diagnosis of shiga toxin-producing Escherichia coli infections [J].
Karch, H ;
Bielaszewska, M ;
Bitzan, M ;
Schmidt, H .
DIAGNOSTIC MICROBIOLOGY AND INFECTIOUS DISEASE, 1999, 34 (03) :229-243
[10]   Development of a monoclonal sandwich ELISA for the detection of animal and human Escherichia coli O157 strains [J].
Kerr, P ;
Chart, H ;
Finlay, D ;
Pollock, DA ;
Mackie, DP ;
Ball, HJ .
JOURNAL OF APPLIED MICROBIOLOGY, 2001, 90 (04) :543-549