Table 2. PCR analysis of key genes of toxigenic V. cholerae O1 strains isolated from environmental samples in Haiti.
Key genes amplified by PCR a | MAMA-PCR b | |||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|
Strains c | ompW | toxR | tcpA CL | tcpA ET | ctxA | ctxB | rstR ET | rstR CL | rstC ET | rstC CL | ctxB CL | ctxB ET |
env894 | + | + | - | + | + | + | + | - | + | - | + | - |
env898 | + | + | - | + | + | + | + | - | + | - | + | - |
env901 | + | + | - | + | + | + | + | - | + | - | + | - |
env949 | + | + | - | + | + | + | + | - | + | - | + | - |
env955 | + | + | - | + | + | + | + | - | + | - | + | - |
env961 | + | + | - | + | + | + | + | - | + | - | + | - |
env1054 | + | + | - | + | + | + | + | - | + | - | + | - |
env1112 | + | + | - | + | + | + | + | - | - | - | + | - |
env1177 | + | + | - | + | + | + | + | - | - | - | + | - |
env1180 | + | + | - | + | + | + | + | - | - | - | + | - |
env1183 | + | + | - | + | + | + | + | - | + | - | + | - |
env1218 | + | + | - | + | + | + | + | - | + | - | + | - |
env1222 | + | + | - | + | + | + | + | - | + | - | + | - |
env1231 | + | + | - | + | + | + | + | - | + | - | + | - |
env1239 | + | + | - | + | + | + | + | - | - | - | + | - |
env1320 | + | + | - | + | + | + | + | - | - | - | + | - |
env1321 | + | + | - | + | + | + | + | - | + | - | + | - |
aGenetic characterization was performed by PCR using convergent primer sets specific for both El Tor and classical V. cholerae O1 strains.
bAll isolates are V. cholerae O1 biotype El-Tor strains carrying classical ctxB gene as determined by MAMA-PCR.
cTwelve (70.6%) of the 17 isolates exhibited the presence of rstC ET genotype