When mice were inoculated orally with 10
0-10
4 cells of mouse-passage descendants of Salmonella typhimurium derived from a carrier-dog feces, the large-intestinal descendant showed the smallest ID
<50> value and was followed by the descendants of the mesenteric lymph node, liver and spleen. A descendant giving a smaller ID
<50> value yielded a large number of colonies having hemagglutinating activity on the blood agar plate. From the colonies, 7 fimbriate and 3 non-fimbriate descendants were selected. The fimbriate descendants having 19 to 91% of fimbriate cells showed various degrees of agglutination with 8 kinds of erythrocytes. The non-fimbriate destendants did not agglutinate the given erythrocytes. There was a tendency among the fimbriate descendants that a descendant with a large number of fimbriate cells gave a smaller ID
<50> value by oral administration against mice (10
1-10
4 cells/mouse). The non-fimbriate descendants were capable of infecting mice rarely by oral administration with 10
1-10
4 cells/mouse. On the contrary, both fimbriate and non-fimbriate descendants gave almost the same LD
<50> value by intraperitoneal inoculation. From statistical analysis on ID
<50> value, it was shown that the infectivity of the large-intestinal descendant was higher than that of a fimbriate descendant with 91% of fimbriate cells isolated from the intestine. The descendants of the mesenteric lymph node and liver were higher in infectivity than any other fimbriate descendant with 50 to 77% of fimbriate cells.
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