Persistence of plasmids, cholera toxin genes, and prophage DNA in classical Vibrio cholerae O1

Infect Immun. 1984 Jul;45(1):222-6. doi: 10.1128/iai.45.1.222-226.1984.

Abstract

Plasmid profiles, the location of cholera toxin subunit A genes, and the presence of the defective VcA1 prophage genome in classical Vibrio cholerae isolated from patients in Bangladesh in 1982 were compared with those in older classical strains isolated during the sixth pandemic and with those in selected eltor and nontoxigenic O1 isolates. Classical strains typically had two plasmids (21 and 3 megadaltons), eltor strains typically had no plasmids, and nontoxigenic O1 strains had zero to three plasmids. The old and new isolates of classical V. cholerae had two HindIII chromosomal digest fragments containing cholera toxin subunit A genes, whereas the eltor strains from Eastern countries had one fragment. The eltor strains from areas surrounding the Gulf of Mexico also had two subunit A gene fragments, which were smaller and easily distinguished from the classical pattern. All classical strains had 8 to 10 HindIII fragments containing the defective VcA1 prophage genome; none of the Eastern eltor strains had these genes, and the Gulf Coast eltor strains contained a different array of weakly hybridizing genes. These data suggest that the recent isolates of classical cholera in Bangladesh are closely related to the bacterial strain(s) which caused classical cholera during the sixth pandemic. These data do not support hypotheses that either the eltor or the nontoxigenic O1 strains are precursors of the new classical strains.

Publication types

  • Comparative Study

MeSH terms

  • Bacteriophages / genetics*
  • Base Sequence
  • Cholera Toxin / genetics*
  • DNA Restriction Enzymes
  • DNA, Bacterial / genetics*
  • DNA, Viral / genetics*
  • Genes*
  • Genes, Bacterial*
  • Nucleic Acid Hybridization
  • Plasmids*
  • Serotyping
  • Species Specificity
  • Vibrio cholerae / genetics*

Substances

  • DNA, Bacterial
  • DNA, Viral
  • Cholera Toxin
  • DNA Restriction Enzymes