Abstract
Detection of diarrhoeagenic Escherichia coli in stool specimens cannot be performed easily in most routine laboratories. This study describes a rapid hybridization assay for identification of enterovirulent Escherichia coli in faecal samples. DNA fragment probes specific for enterotoxigenic Escherichia coli, Vero cytotoxin producing Escherichia coli and enteropathogenic Escherichia coli were labelled with digoxigenin and produced in large quantities by polymerase chain reaction. Stool samples were cultured overnight, replica-plated and hybridized with five different probes. This method gives satisfactory results, requires a minimum number of bacteria subcultures and may be used routinely in the laboratory.
Original language | English |
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Pages (from-to) | 121-127 |
Number of pages | 7 |
Journal | Journal of Microbiological Methods |
Volume | 15 |
Issue number | 2 |
Publication status | Published - Apr 1992 |
Keywords
- NONRADIOACTIVELY LABELED PROBE
- ENTEROTOXIGENIC ESCHERICHIA-COLI
- VERO CYTOTOXIN PRODUCING ESCHERICHIA-COLI
- ENTEROPATHOGENIC ESCHERICHIA-COLI
- STABLE ENTERO-TOXIN
- HEAT-LABILE TOXIN
- COLONY HYBRIDIZATION
- GENE PROBES
- NUCLEOTIDE-SEQUENCE
- IDENTIFICATION
- DIARRHEA
- STRAINS
- POLYNUCLEOTIDE
- CLONING