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Infection and Immunity, March 2001, p. 1306-1314, Vol. 69, No. 3
VA Medical Center and Department of Medicine,
University of Minnesota, Minneapolis, Minnesota
Received 12 July 2000/Returned for modification 26 October
2000/Accepted 20 November 2000
To test the canine reservoir hypothesis of extraintestinal
pathogenic Escherichia coli (ExPEC), 63 environmental
canine fecal deposits were evaluated for the presence of ExPEC by a
combination of selective culturing, extended virulence genotyping,
hemagglutination testing, O serotyping, and PCR-based phylotyping.
Overall, 30% of canine fecal samples (56% of those that yielded
viable E. coli) contained papG-positive
E. coli, usually as the predominant E. coli
strain and always possessing papG allele III (which encodes variant III of the P-fimbrial adhesin molecule PapG). Multiple other
virulence-associated genes typical of human ExPEC were prevalent among
the canine fecal isolates. According to serotyping, virulence genotyping, and random amplified polymorphic DNA analysis, over 50% of
papG-positive fecal E. coli could be directly
correlated with specific human clinical isolates from patients with
cystitis, pyelonephritis, bacteremia, or meningitis, including
archetypal human ExPEC strains 536, CP9, and RS218. Five canine fecal
isolates and (clonally related) archetypal human pyelonephritis isolate 536 were found to share a novel allele of papA (which
encodes the P-fimbrial structural subunit PapA). These data confirm
that ExPEC representing known virulent clones are highly prevalent in
canine feces, which consequently may provide a reservoir of ExPEC for
acquisition by humans.
0019-9567/01/$04.00+0 DOI: 10.1128/IAI.69.3.1306-1314.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
Canine Feces as a Reservoir of Extraintestinal
Pathogenic Escherichia coli
*
Corresponding author. Mailing address: Infectious
Diseases (111F), VA Medical Center, 1 Veterans Dr., Minneapolis, MN
55417. Phone: (612) 725-2000, ext. 4185. Fax: (612) 725-2273. E-mail: johns007{at}tc.umn.edu.
Present address: University of Minnesota Medical School,
Minneapolis, Minn.
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