ABSTRACT. Epidemiology of canine enteric infections was studied. Rectal swabs collected from 95 dogs presented at animal hospitals during a period from January to June of 2000 were examined for enteric pathogens, including viruses and Giardia lamblia (G. lamblia). Most frequently detected in both diarrheal and normal feces were canine coronavirus (55.4%) and G. lamblia (48.2%). Canine parvovirus type 2 (CPV-2) was specifically associated with diarrheal cases and CPV-2b was the predominant antigenic type. Although canine rotavirus, canine adenovirus, and canine distemper virus were also detected in a small number of diarrheal cases, no evidence for calicivirus infection was obtained. KEY WORDS: canine coronavirus, canine parvovirus, Giardia lamblia.J. Vet. Med. Sci. 63(5): 573-575, 2001 Type 2 canine parvovirus (CPV-2), canine distemper virus (CDV) and canine adenovirus type 1 (CAV-1) have been well established as primary enteric viral pathogens of dogs. Secondly, canine coronavirus (CCV) as well as canine rotavirus (CRV) have been more recently documented [12]. In this communication, we describe etiology of current canine diarrheal cases in Japan in consideration of more efficacious preventive measures matching the existing epidemiological status.A total of 95 rectal swab specimens were taken from dogs, and the samples consisted of 85 diarrheal and 10 normal stools. These samples were submitted by animal hospitals in various locations of the country (Hokkaido, Miyagi, Fukushima, Ibaraki, Tokyo, Kanagawa, Shizuoka, Osaka, Okayama, and Fukuoka) during a period from January to June of 2000. Ages of dogs were between 28 days and 4 years, and the average was 4.1 months old. Two swab specimens were taken from each patient, and one was used for virus examination and the other for Giardia lamblia (G. lamblia) detection by enzyme-linked immunosorbent assay (ELISA). Stool was also examined for Giardia cysts by a zinc sulfate centrifugation flotation method at each animal hospital.Swabs were placed in 2 ml of Eagle's minimal essential medium, extracts were clarified by centrifugation at 15,000 rpm for 20 min, and the resulting supernatants were examined for viruses.For detection of CRV, reverse passive hemagglutination assay (RPHA) and virus isolation by using MA104 cell culture were used, and the methods have been described previously [15]. Two diarrheal specimens were found to be CRV antigen-positive by RPHA as shown in Table 1. Antigenic type G3P [3] rotavirus strain KSD-88 belonging to the K9 genogroup, determined by sequencing, PCR, and RNA-RNA hybridization assays described elsewhere [17,18], was isolated from one specimen, but not from the other because of interference by bacterial contamination in the cell culture. The detection rate of CRV in the present study was low as that of the previous survey [12] and the antigenic type was the same as the previous rotavirus isolates reported [18].For detection of CCV, reverse transcriptase-PCR (RT-PCR) assay and virus isolation by using fcwf-4 cell culture were used, and...