Publication | Open Access
Detection of Various Variant Verotoxin Genes in <i>Escherichia coli</i> by Polymerase Chain Reaction
127
Citations
29
References
1993
Year
EngineeringPathogen DetectionMicrobial PathogensGeneticsMolecular BiologyBacterial PathogensVtec InfectionPolymerase Chain ReactionDesigned Common PrimersMolecular DiagnosticsMicrobial ToxinFoodborne PathogensPathogen CharacterizationMolecular MicrobiologyClinical MicrobiologyMolecular Diagnostic TechniquesCommon PrimersPathogenesisMicrobiologyMedicineDiagnostic MicrobiologyMicrobial Genetics
Abstract We constructed common primers for the polymerase chain reaction to detect the genes for various Verotoxins reported, that is, VT1 (or SLT‐I), VT2 (or SLT‐II), VT2vha, VT2vhb, SLT‐IIv (or VT2vp1, VTe) and SLT‐IIva (or VT2vp2). A total of 80 Verocytotoxin‐producing Escherichia coli strains isolated from humans, domestic animals and meats gave a positive result by PCR with the designed common primers. Digestion by restriction endonucleases Bgl II and Eco T14I of the amplicon of the VT2vp2 gene gave specific bands of the expected sizes, but not of the amplicons of other VT genes, suggesting a possible method for identification of the VT2vp2 gene. Application of the PCR with the designed primers in diagnostic and epidemiological studies on VTEC infection is also discussed.
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