Hk. Parmentier et al., LOW-MOLECULAR-WEIGHT COOPERIA-ONCOPHORA ANTIGENS - CHARACTERIZATION AND HUMORAL IMMUNE-RESPONSES IN CALVES MONO-INFECTED WITH 100000 INFECTIVE LARVAE, Veterinary parasitology, 59(3-4), 1995, pp. 219-230
Characteristics of the humoral immune response of Cooperia oncophora-i
nfected calves to low molecular weight antigens of C. oncophora were s
tudied. Immunoblotting with sera obtained from calves 6 weeks after a
single oral infection with 100 000 third-stage (L(3)) C. oncophora lar
vae revealed several corresponding antigenic fragments between adult w
orms and the fourth-stage (L(4)) larvae. No reactivity in the immune s
era was found against the L(3) stage. A previously defined complex of
low molecular weight proteins (12-15 kDa) was found on both L, and adu
lt Cooperia stages, but not on the L(3) stage. C. oncophora adults dif
fered from the L(4) larvae at the 31/32 and 37 kDa level. Several adul
t and L(4) proteins were bound by biotinylated Concanavalin A, as was
also true for L(3) proteins. A 31/32 kDa glycoprotein of adult worms w
as recognised by a monoclonal antibody with specificity for phosphoryl
choline. Using monoclonal antibodies in ELISA and Western blotting, th
e serum antibody response of C. oncophora-infected calves to adult wor
m antigen was almost entirely IgG1. Binding of the IgG1 antibodies was
restricted to a complex of reduced 12-15 kDa protein(s) and a 27 kDa
fragment of adult worms. The data suggest that the systemic humoral im
mune response of calves during a primary infection with C. oncophora c
onsists mainly of an IgG1 response, and is directed to a non-glycosyla
ted Cooperia protein (molecular weight estimated at 12-15 kDa under re
ducing conditions and 18 kDa under nonreducing conditions). This prote
in is probably present in both L(4) larvae and adults. Since it was no
t bound by immune sera from calves mono-infected with several other ne
matodes, the 12-15 kDa protein complex may represent a Cooperia-specif
ic component that can be used for serodiagnosis.