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Validity of SmaI-defined genotypes of Campylobacter jejuni examined by SalI, KpnI, and BamHI polymorphisms: evidence of identical clones infecting humans, poultry, and cattle

Published online by Cambridge University Press:  01 June 1998

S. L. W. ON
Affiliation:
Danish Veterinary Laboratory, Bülowsvej 27, DK-1790 Copenhagen V, Denmark
E. M. NIELSEN
Affiliation:
Danish Veterinary Laboratory, Bülowsvej 27, DK-1790 Copenhagen V, Denmark
J. ENGBERG
Affiliation:
Statens Serum Institut, Artillerivej 5, DK-2300 Copenhagen S, Denmark
M. MADSEN
Affiliation:
Danish Veterinary Laboratory, Hangøvej 2, DK-8200 Aarhus N, Denmark
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Abstract

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We describe here an examination of the validity of molecular types of Campylobacter jejuni as defined by separation of SmaI-digested DNA using pulsed-field gel electrophoresis (PFGE), recently suggested as part of a molecular subtyping scheme. Thirty-four Danish strains from humans, 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 PFGE of SalI, KpnI and BamHI-digested DNA, and also by serotyping with heat-stable antigens. All outbreak-related strains were indistinguishable by all criteria, as were two sets of two randomly-isolated human strains. Two groups of indistinguishable isolates contained randomly isolated strains from more than one source (poultry, humans and/or cattle), a finding with significant epidemiological connotations. All ‘genetically identical’ strains belonged to the same serotype, whereas genetic differences were detected between strains assigned to the same SmaI PG but differing in serotype. We conclude that PFGE-based genetic fingerprinting can yield invaluable data for epidemiological studies of sporadic C. jejuni infection, but that results based on one restriction site polymorphism must be checked with another enzyme.

Type
Research Article
Copyright
1998 Cambridge University Press

Footnotes

This paper was presented in part, at the 9th International Workshop on Campylobacter, Helicobacter and related organisms in Cape Town, South Africa, 15–19 September 1997 as abstract G17 (p. 36 of the abstract book).