To compare between biotype of
Vibrio cholerae O1 and genotype using polymerase chain reaction (PCR), 9 classical and 81 El Tor biovar strains were investigated for hemolysis, agglutination of avian erythrocytes. VP test reactivity, sensitivity to both polymyxin B and classical phage IV, and genotype using PCR amplification of
hlyA, tcpA, rtxA and
rtxC. One classical biovar strain showed atypical reaction upon agglutination of avian erythrocytes. Eighteen El Tor biovarstrains showed atypical reactions, with the exception of sensitivity to polymyxin B. By PCR detection of
hlyA, rtxA and
rtxC amplifications, all classical biovar strains possessed only classical type
hlyA, while all El Tor biovar strains possessed El Tor type
hlyA, rtxA and
rtxC. By PCR analysis of amplicons, all classical biovar strains possessed classical type
tcpA. One
ctx-negative El Tor biovar strain possessed degenerated classical type
tcpA and 4
ctx-negative El Tor biovar strains had no detectable
tcpA.
These results indicated that genotype of
V. cholerae O1 using PCR detection of
hlyA, rtxA and
rtxC was consistent with biotype of the organism, suggesting that analysis of the genotype of the organism was as effective as by biochemical properties. However, PCR detection of
hlyA is most appropriate for the biotyping of
V. cholerae O1, as compared to biochemical properties, since El Tor biovar was originally distinguished from classical biovar strains by the hemolytic reaction.
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