Detection of enterotoxigenic Escherichia coli, Shigella and Campylobacter spp. by multiplex PCR assay

J Diarrhoeal Dis Res. 1996 Sep;14(3):207-10.

Abstract

Three oligonucleotide primers were used in a polymerase chain reaction (PCR) assay for the simultaneous amplification of regions of the invasive plasmid antigen (ipaH) of Shigella spp., flagellin gene (flaA) of Campylobacter spp., and heat-labile enterotoxin (LT) of enterotoxigenic Escherichia coli (ETEC). The multiplex assay was performed using DNA extracted by a chaotropic method directly from diarrhoeal stools. The diagnostic efficacy of the assay was analyzed by agarose gel electrophoresis. This assay shows a novel approach for the diagnosis of diarrhoea caused by Shigella spp., ETEC, and Campylobacter spp.

Publication types

  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Campylobacter / classification
  • Campylobacter / genetics
  • Campylobacter / isolation & purification*
  • DNA Primers / genetics
  • DNA, Bacterial / genetics
  • Escherichia coli / classification
  • Escherichia coli / genetics
  • Escherichia coli / isolation & purification*
  • Feces / microbiology*
  • Humans
  • Polymerase Chain Reaction / methods*
  • Shigella / classification
  • Shigella / genetics
  • Shigella / isolation & purification*

Substances

  • DNA Primers
  • DNA, Bacterial