RECOMBINANT CHICKEN INTERFERON-GAMMA-MEDIATED INHIBITION OF EIMERIA-TENELLA DEVELOPMENT IN-VITRO AND REDUCTION OF OOCYST PRODUCTION AND BODY-WEIGHT LOSS FOLLOWING EIMERIA-ACERVULINA CHALLENGE INFECTION
Hs. Lillehoj et Kd. Choi, RECOMBINANT CHICKEN INTERFERON-GAMMA-MEDIATED INHIBITION OF EIMERIA-TENELLA DEVELOPMENT IN-VITRO AND REDUCTION OF OOCYST PRODUCTION AND BODY-WEIGHT LOSS FOLLOWING EIMERIA-ACERVULINA CHALLENGE INFECTION, Avian diseases, 42(2), 1998, pp. 307-314
Recombinant chicken interferon-gamma (chIFN-gamma) was produced in CHO
-K1 or Spodoptera frugiperda (SF9) insect cells by transfect ion with
a pcDNA vector or recombinant baculovirus (SF9-interferon-gamma [IFN-g
amma]) carrying the chIFN-gamma gene. A rabbit antibody against a synt
hetic peptide corresponding to an immunogenic portion of chIFN-gamma r
ecognized a 22-23-kDa band in SF3-IFN-gamma cell extracts by western b
lot analysis. Biological activity of recombinant chIFN-gamma was shown
by its inhibition of vesicular stomatitis virus-induced cytotoxicity
of chicken embryonic fibroblast cells in vitro. To investigate the rol
e of chIFN-gamma during Eimeria infection, CHCC-OU2 chicken cells eith
er pretreated with chIFN-gamma or stably transfected with the chIFN-ga
mma gene were infected with Eimeria tenella sporozoites. IFN-gamma dem
onstrated significant reductions in intracellular sporozoite developme
nt without affecting sporozoite invasion of host cells. Furthermore, c
hickens treated with recombinant chIFN-gamma showed decreased oocyst p
roduction and significant improvement in body weight gain following Ei
meria acervulina challenge infection. These results provide the first
direct evidence that chIFN-gamma exerts an inhibitory effect against E
imeria and provides a rational basis for use of this cytokine as a vac
cine adjuvant against coccidiosis.