Dn. Cameron et al., MOLECULAR CHARACTERIZATION OF VIBRIO-CHOLERAE O1 STRAINS BY PULSED-FIELD GEL-ELECTROPHORESIS, Journal of clinical microbiology, 32(7), 1994, pp. 1685-1690
Pulsed-field gel electrophoresis (PFGE) was performed on 180 isolates
of Vibrio cholerae serogroup 01 representing 6 different multilocus en
zyme electrophoresis (MEE) types and 27 rRNA restriction fragment leng
th polymorphism types (ribotypes). Isolates were digested with the res
triction enzyme NotI and were separated into 63 patterns on the basis
of differences in band arrangements. In general, strains which were di
fferent by MEE or ribotyping also had different PFGE patterns. PFGE id
entified individual strains within a single MEE type or ribotype; isol
ates with one PFGE pattern were less frequently distinguished by ribot
yping. All V. cholerae 01 isolates tested from the Latin American epid
emic were indistinguishable by their MEE, ribotype, or PFGE patterns.
PFGE could further distinguish strains of this same ribotype isolated
in Africa, Europe, the South Pacific, or Southeast Asia. Although both
MEE and PFGE could identify the strain from the Latin American epidem
ic, PFGE was more rapid and less labor intensive. PFGE also distinguis
hed nontoxigenic isolates endemic to the U.S. Gulf Coast from unrelate
d nontoxigenic isolates. In the present study PFGE was more discrimina
ting than other previously described subtyping assays for V. cholerae
01 and appears to be a useful epidemiologic tool.