Br. Madewell et al., Clostridium difficile: a survey of fecal carriage in cats in a veterinary medical teaching hospital, J VET D INV, 11(1), 1999, pp. 50-54
Fecal samples collected from 245 cats over a 6-month period were analyzed f
or the presence of Clostridium difficile. After culture on selective media,
isolates were identified by a latex agglutination test, and the presence o
f toxin A and toxin B gene sequences was determined by polymerase chain rea
ction. Clostridium difficile was isolated from 23 (9.4%) of the cats, and 3
4.8% of that group were colonized with toxigenic strains. All of the cats c
olonized with toxigenic C. difficile had greater than or equal to 1 of the
risk factors (antibiotic use, antineoplastic therapy, immunosuppressive vir
us infection) associated with C. difficile infection in humans. Clostridium
difficile was not found in any of the cats from a clinically healthy outpa
tient group of cats examined from the same hospital nor in cats from a spec
ific-pathogen-free research colony on the same campus tested during the sam
e time period. The data obtained in this study confirm the presence of C. d
ifficile in cats at a veterinary teaching hospital. DNA fingerprinting anal
ysis of these isolates allowed separation of the strains into 5 groups. Typ
e 4 strain found in 7 cats was also recovered from the floor drain in the s
ame hospital, suggesting a possible source of infection. Whether the organi
sm is of clinical significance in diarrheal diseases of cats remains to be
determined.