Use of automated sequencing of polymerase chain reaction-generated amplicons to identify three types of cholera toxin subunit B in Vibrio cholerae O1 strains

J Clin Microbiol. 1993 Jan;31(1):22-5. doi: 10.1128/jcm.31.1.22-25.1993.

Abstract

Cholera toxin is the principal factor causing the profuse intestinal fluid secretion that is characteristic of cholera. The DNA sequences of the cholera toxin subunit B structural genes from 45 Vibrio cholerae O1 strains isolated in 29 countries over a period of 70 years were determined by automated DNA sequencing of polymerase chain reaction-generated amplicons. Three types of cholera toxin B subunit gene (ctxB) were identified. Genotype 1 was found in strains of classical biotype worldwide and El Tor biotype strains associated with the U.S. Gulf Coast, genotype 2 was found in El Tor biotype strains from Australia, and genotype 3 was found in El Tor biotype strains from the seventh pandemic and the recent Latin American epidemic. All base changes correspond to an amino acid substitution in the B subunit of the cholera toxin. Heterogenicity in the B subunit could have implications for vaccine development and diagnostic tests for cholera toxin and antitoxin. We conclude that this technology provides timely and potentially useful epidemiological information.

MeSH terms

  • Africa / epidemiology
  • Americas / epidemiology
  • Asia / epidemiology
  • Australia / epidemiology
  • Base Sequence
  • Cholera / epidemiology
  • Cholera Toxin / chemistry
  • Cholera Toxin / genetics*
  • DNA, Bacterial / genetics
  • Genes, Bacterial
  • Genetic Variation
  • Humans
  • Molecular Sequence Data
  • Polymerase Chain Reaction
  • Sequence Analysis, DNA / methods
  • Vibrio cholerae / classification*
  • Vibrio cholerae / genetics*

Substances

  • DNA, Bacterial
  • Cholera Toxin