Microbiology and Immunology · 2005 · 63 citations · 29 references
Life SciencesMicrobiologyMolecular BiologyDiagnostic MicrobiologyHost-pathogen InteractionsMolecular DiagnosticsPathogen DetectionPathogen GenomicsPathogen Virulence FactorsPolymerase Chain ReactionVirulence GenomicsBacterial Virulence GenesEscherichia ColiMolecular Diagnosis Of Enteric PathogensMultiplex Polymerase Chain Reaction (Pcr)Multiplex Polymerase Chain Reaction AssaysVirulence Gene AnalysisVirulence Gene DetectionVirulence Gene Identification
A one-shot multiplex polymerase chain reaction (PCR) was developed for detecting 12 virulence genes of diarrheagenic Escherichia coli. In order to differentiate between the five categories of diarrheagenic E. coli, we selected the target genes: stx1, stx2, and eaeA for enterohemorrhagic E. coli(EHEC); eaeA, bfpA, and EAF for enteropathogenic E. coli(EPEC); invE for enteroinvasive E. coli(EIEC); elt, estp, and esth for enterotoxigenic E. coli(ETEC); CVD432 and aggR for enteroaggregative E. coli(EAggEC); and astA distributed over the categories of diarrheagenic E. coli. In our multiplex PCR system, all 12 targeted genes (stx1, stx2, eaeA, invE, elt, estp, astA, esth, bfpA, aggR, EAF, and CVD432) were amplified in a single PCR reaction in one tube and detected by electrophoresis. Using our multiplex PCR, the 208 clinically isolated strains of diarrheagenic E. coli in our laboratory were successfully categorized and easily analyzed for the presence of virulence plasmids.
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Manual of Clinical Microbiology
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