Characterization of enterotoxigenic Escherichia coli (ETEC) has been based
almost exclusively on the detection of phenotypic traits such as serotypes
and virulence-associated factors: heat-labile (LT) and heat-stable (ST) tox
ins and colonization factors (CFs). In the present work we show that the an
alysis of band patterns generated by randomly amplified polymorphic DNA (RA
PD) analysis and pulsed-field gel electrophoresis (PFGE) of digested chromo
somal DNA can be used to detect genetic diversity among ETEC strains expres
sing identical phenotypic traits. The study included 29 ETEC isolates from
Latin America and Spain expressing the phenotype O153:H45 CFA/I ST plus 1 r
ough derivative, 2 nonmotile derivatives, and 1 O78:H12 CFA/I ST isolate, a
nd a representative of a genetically distinct ETEC group. The results showe
d that the O153:H45 CFA/I ST ETEC isolates belong to a single clonal cluste
r whose isolates share on average, 84% of the RAPD bands and 77% of the PFG
E restriction fragments, while the O78:H12 isolate shared only 44 and 4% of
the RAPD bands and PFGE fragments, respectively, with the isolates of the
O153:H45 group. More relevantly, RAPD and PFGE fingerprints disclosed the p
resence of different clonal lineages among the isolates of the O153:H45 clu
ster. Some of the genetic variants were isolated from defined geographic ar
eas, while places like Sao Paulo City in Brazil and the middle-eastern part
of Argentina were populated by several genetic variants of related, but no
t identical, ETEC strains. These results show that molecular biology-based
typing methods can disclose strain diversity, which is usually missed in st
udies restricted to phenotypic typing of ETEC.