VALIDITY OF SMAI-DEFINED GENOTYPES OF CAMPYLOBACTER-JEJUNI EXAMINED BY SALI, KPNI, AND BAMHI POLYMORPHISMS - EVIDENCE OF IDENTICAL CLONES INFECTING HUMANS, POULTRY, AND CATTLE
Slw. On et al., VALIDITY OF SMAI-DEFINED GENOTYPES OF CAMPYLOBACTER-JEJUNI EXAMINED BY SALI, KPNI, AND BAMHI POLYMORPHISMS - EVIDENCE OF IDENTICAL CLONES INFECTING HUMANS, POULTRY, AND CATTLE, Epidemiology and infection, 120(3), 1998, pp. 231-237
We describe here an examination of the validity of molecular types of
Campylobacter jejuni as defined by separation of SmaI-digested DNA usi
ng pulsed-held gel electrophoresis (PFGE), recently suggested as part
of a molecular subtyping scheme. Thirty-four Danish strains from human
s, water, poultry and cattle were assigned to one of six SmaI 'profile
groups' (PGs), with two additional strains included as genotypically
distinct controls. The interstrain relationships were reexamined by PF
GE of SalI, KpnI and BamHI-digested DNA, and also by serotyping with h
eat-stable antigens. All outbreak-related strains were indistinguishab
le by all criteria, as were two sets of two randomly-isolated human st
rains. Two groups of indistinguishable isolates contained randomly iso
lated strains from more than one source (poultry, humans and/or cattle
), a finding with significant epidemiological connotations. All 'genet
ically identical' strains belonged to the same serotype, whereas genet
ic differences were detected between strains assigned to the same SmaI
PG but differing in serotype. We conclude that PFGE-based genetic fin
gerprinting can yield invaluable data for epidemiological studies of s
poradic C. jejuni infection, but that results based on one restriction
site polymorphism must be checked with another enzyme.