4.4 Article

Identification of Escherichia coli O157:H7 and other enterohemorrhagic serotypes by EHEC-hlyA targeting, strand displacement amplification, and fluorescence polarization

Journal

MOLECULAR AND CELLULAR PROBES
Volume 16, Issue 2, Pages 85-92

Publisher

ACADEMIC PRESS LTD ELSEVIER SCIENCE LTD
DOI: 10.1006/mcpr.2001.0389

Keywords

rapid detection; enterohemorrhagic E coli; strand displacement amplification; fluorescence polarization

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Human disease caused by enterohemorrhagic E. coli O157:H7 and other serotypes (EHEC) has been associated with bovine fecal contamination of food and the environment. The range of serotypes, low infectious dose, and numerous transmission vehicles for EHEC render development of detection methods for this pathogen complex. In this study, the hemolysin gene (EHEC-hlyA) was targeted with oligonucleoticles, and probe-target hybrids were amplified using strand displacement amplification (SDA). Amplicons were resolved in the complete reaction mix through changes in the fluorescence polarization (FP) of a fluorescein-labeled detector probe hybridized to the amplicons during amplification. Results combining EHEC-hlyA, SDA, and FP were obtained within 35 min of reaction initiation. The test specificity was determined on EHEC strains representing 13 serotypes (49 isolates); and control uropathogenic, commensal, and other organisms (10 isolates). Statistical analysis of results indicated a sensitivity in the reaction vessel to 4.3 bacteria (95% confidence interval), and a specificity for EHEC (n=59) at 100% (P=5.11 E-17; i.e. Pmuch less than0.05). Detection based on combining EHEC-hlyA, SDA, and FP was compatible with water sources directly associated with human infection (drinking and recreational Supplies), and bovine drinking trough water representing an environmental matrix linked to the maintenance of an EHEC animal reservoir. (C) 2002 Elsevier Science Ltd.

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