PRODUCTION OF GILL-ASSOCIATED AND SERUM ANTIBODY BY RAINBOW-TROUT (ONCORHYNCHUS-MYKISS) FOLLOWING IMMERSION IMMUNIZATION WITH ACETONE-KILLED FLAVOBACTERIUM-BRANCHIOPHILUM AND THE RELATIONSHIP TO PROTECTION FROM EXPERIMENTAL CHALLENGE
Js. Lumsden et al., PRODUCTION OF GILL-ASSOCIATED AND SERUM ANTIBODY BY RAINBOW-TROUT (ONCORHYNCHUS-MYKISS) FOLLOWING IMMERSION IMMUNIZATION WITH ACETONE-KILLED FLAVOBACTERIUM-BRANCHIOPHILUM AND THE RELATIONSHIP TO PROTECTION FROM EXPERIMENTAL CHALLENGE, Fish & shellfish immunology, 5(2), 1995, pp. 151-165
Rainbow trout (Oncorhynchus mykiss) were either injected twice intrape
ritoneally with 0.1 ml of a 1:10 dilution from broth culture of aceton
e-killed Flavobacterium branchiophilum, immersed twice for 1 h in a 1:
10, 1:100 or 1:1000 dilution from a broth culture of acetone-killed F.
branchiophilum, or utilized as unexposed controls. After bath challen
ge with live F. branchiophilum the percent cumulative mortality of eac
h group was as follows; controls, 45.3%, i.p.-injected, 32.1%; immerse
d in a 1:1000 dilution, 38.0%; immersion in a 1:100, 40.9%; and immers
ion in a 1:10 dilution, 11.7%. There was no relationship between the g
roup treatment and the levels of F. branchiophilum antigen detected by
enzyme immunoassay following challenge. The amount of gill-associated
and serum antibody to F. branchiophilum detected in the immersion imm
unized groups before challenge increased with increasing concentration
of antigen in the bath. The i.p.-injected group had the highest serum
antibody of any group while gill-associated antibody was comparable t
o those groups which were bath exposed with the lower concentrations o
f F. branchiophilum antigen. A similar pattern of antibody response wa
s seen with five groups of rainbow trout treated exactly as the five g
roups above, in which antibody was monitored over time, but which were
not challenged. Gill-associated and serum antibody were detectable fo
llowing primary antigen exposure regardless of route. The serum and gi
ll-associated antibody responses were present for longer following a s
econd antigen exposure by the same route, and the gill-associated but
not the serum antibody was increased over those following primary anti
gen exposure. The greatest increase in gill-associated antibody respon
se was seen in the group which received the highest concentration of a
ntigen via bath.