Recently, a number of cases of human infections due to Yersinia enterocolitica have been reported in many countries, and much attention has been given to the organism as one of the important etiologic agents of enteritis, appendicitis, septicemia, arthritis and others (12). In most of the sporadic cases or outbreaks, however, the source and the route of the infection remained unknown, since ecology of the organism has not yet been understood clearly.The authors studied previously the distribution of Y. enterocolitica in healthy humans, livestock, foodstaff and the natural environment (14,15). Through these investigations, it was found that Y. enterocolitica was isolated from swine and rats at a high rate, and over 70% of the isolates were of the same serovars as those from human cases. These findings suggested the importance of swine as one of the infective sources for humans.In the present survey, distribution of Y. enterocolitica in dogs and cats, which have close relations to humans as pet animals, was investigated to obtain more extensive ecological informations of the organism. These animals were also examined for the presence of Y. pseudotuberculosis. A total of 704 stray or unwanted adult dogs and 373 unwanted adult cats obtained from the Tokyo Metropolitan Dog Pound Office were submitted to the survey. The dogs were examined between October 1974 and September 1976, and the cats between June 1975 and September 1976.Autopsies were made immediately after the sacrifice, and about 1 g each of the ileo-cecal contents, rectal contents and mesenteric lymph node was sampled. The content to be tested was suspended into 5 ml of sterile saline, and the mesentric lymph node was homogenized with 10 ml of sterile saline. A loopful of each specimen thus prepared was directly plated on both SS and MacConkey agar plates, and incubated at 25 C for 48 hr. Enrichment cultures were also made by inoculating 1 ml of each specimen into 20 ml of 1/15 M phosphate buffer solution (pH 7.6), and incubated at 4 C for 21 days. After the cold enrichment, a loopful of each culture was spread on the agar plates, and incubated at 25 C for 48 hr. Suspicious colonies grown on the agar plates were identified by the method described previously (14). The biovars of Y. enterocolitica were determined according to the scheme and method described by Wauters (11) .Summarized results are shown in Table 1. Y. enterocolitica was isolated from 42 643