These parameters were assayed by means of colony forming units test (CFU) a
nd the Limulus Amebocyte Lysate test (LAL), respectively. Birds were infect
ed per os with 1,5 x 10(9) CFU/ml of wild strain of S. gallinarum isolated
from a dead hen. Approximately 1,5 x 10(2); 1,3 x 10(2) and 1,2 x 10(2) CFU
of S. gallinarum were recorded from 1 g of liver, 1 g of spleen and 1 ml o
f blood from the chickens on day 1 post infection. By day 4 corresponding d
ata were 3,7 x 10(4): 4,8 x 10(3) and 1,1 x 10(3) respectively and on day 7
10(5) CFU were present in all three specimen types. The liver and spleen o
f dead birds were contaminated with more than 10(7)CFU per g. The endotoxin
from S. gallinarum was found to have an activity of 1,5; 12,0 and 15,0 end
otoxin units (EU)/ml on day 1, 4 and 7 after infection, respectively. No en
dotoxin activity was established in the blood of the control group (before
infection) by the LAL test. This is the first time the connection between t
he amount of live S. gallinarum in the blood, liver and the circulating lev
el of endotoxin in the blood during the infectious stage of experimental ac
ute fowl typhoid, has been demonstrated.