CLAMPED HOMOGENOUS ELECTRIC-FIELDS (CHEF) GEL-ELECTROPHORESIS OF DNA RESTRICTION FRAGMENTS FOR COMPARING GENOMIC VARIATIONS AMONG STRAINS OF YERSINIA-ENTEROCOLITICA AND YERSINIA SPP
C. Buchrieser et al., CLAMPED HOMOGENOUS ELECTRIC-FIELDS (CHEF) GEL-ELECTROPHORESIS OF DNA RESTRICTION FRAGMENTS FOR COMPARING GENOMIC VARIATIONS AMONG STRAINS OF YERSINIA-ENTEROCOLITICA AND YERSINIA SPP, Zentralblatt fur Bakteriologie, 281(4), 1994, pp. 457-470
Yersinia enterocolitica gastroenteritis was first recognized in the ea
rly 1960s and has since been reported with increasing frequency. To de
termine if strains of Y. enterocolitica, within a restricted region is
olated over 8 years (1985-1993), originated from a single or multiple
clones, pulsed-field gel electrophoresis (PFGE) of large chromosomal D
NA restriction fragments generated by XbaI or NotI was used. A total o
f 27 isolates of Y. enterocolitica were analyzed, 24 from Austria (Vie
nna and Graz) consisting of serogroups 0:3 (17 isolates), 0:9 (6 isola
tes), 0:5 (1 isolate); 2 from Germany of serogroups 0:3 and 0:9 (1 iso
late each); 1 from the U.S.A. of serogroup 0:8. Genomic fingerprints o
f these strains were compared to those of 8 other Yersinia species to
ascertain if their restriction endonuclease digestion profiles (REDP)
were serogroup and/or species specific. The 27 Y. enterocolitica strai
ns could be divided into 16 genomic varieties according to their restr
iction patterns with NotI and XbaI. PFGE was highly discriminatory as
strains belonging to the same serogroup could be subdivided into diffe
rent genomic groups. Furthermore, Y. enterocolitica strains isolated f
rom the same region, over an 8 year period, belonged to a few closely
related clones. The genomic fingerprints of Yersinia were found to be
species and serogroup specific.