The presence of a Salmonella serotype Enteritidis repeat element (SERE
) located within the upstream regulatory region of the sefABCD operon
encoding fimbrial proteins is reported. DNA dot-blot hybridisation ana
lyses and computerised searches of genetic databases indicate that SER
E is well conserved and widely distributed throughout the bacterial an
d archaeal kingdoms. A SERE-based polymerase chain reaction (SERE-PCR)
assay was developed to fingerprint 54 isolates of Enteritidis represe
nting nine distinct phage types and 54 isolates of other Salmonella se
rotypes. SERE-PCR identified five distinct fingerprint profiles among
the 54 Enteritidis isolates; no correlation between phage types and SE
RE-PCR fingerprint patterns was noticed. SERE-PCR was reproducible, ra
pid and easy to perform. The results of this investigation suggest tha
t the limited heterogeneity of SERE-PCR fingerprint patterns can be ut
ilised to develop serotype-and serogroup-specific fingerprint patterns
for isolates of Enteritidis.