To test the canine reservoir hypothesis of extraintestinal pathogenic Esche
richia 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-base
d phylotyping. Overall, 30% of canine fecal samples (56% of those that yiel
ded viable E. coli) contained papG-positive E. coli, usually as the predomi
nant E. coli strain and always possessing papG allele III (which encodes va
riant III of the P-fimbrial adhesin molecule PapG). Multiple other virulenc
e-associated genes typical of human ExPEC were prevalent among the canine f
ecal isolates. According to serotyping, virulence genotyping, and random am
plified polymorphic DNA analysis, over 50% of papG-positive fecal E. coli c
ould be directly correlated with specific human clinical isolates from pati
ents with cystitis, pyelonephritis, bacteremia, or meningitis, including ar
chetypal human ExPEC strains 536, CP9, and RS218. Five canine fecal isolate
s and (clonally related) archetypal human pyelonephritis isolate 536 were f
ound to share a novel allele of papA (which encodes the P-fimbrial structur
al subunit PapA). These data confirm that ExPEC representing known virulent
clones are highly prevalent in canine feces, which consequently may provid
e a reservoir of ExPEC for acquisition by humans.