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J Clin Microbiol. 1993 January; 31(1): 22-25

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

O Olsvik, J Wahlberg, B Petterson, M Uhlén, T Popovic, I K Wachsmuth and P I Fields

Division of Bacterial and Mycotic Diseases, Centers for Disease Control, Atlanta, Georgia 30333.

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.


J Clin Microbiol. 1993 January; 31(1): 22-25




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Copyright © 1993 by the American Society for Microbiology. All rights reserved.