The present study was undertaken to increase the yield of Eimeria tene
lla oocysts in primary chicken kidney cells (PCKCs) using a comparativ
ely inexpensive cell-culture system. PCKCs growing on coverslips posit
ioned on the bottoms of individual wells in 24-well tissue-culture pla
tes were infected with sporozoites of E. tenella. The effects of chang
ing the culture medium (RPMI 1640), medium pH, serum type, and serum c
oncentration in the wells were determined by counting newly produced o
ocysts at 7 days postinoculation. There were significantly more (P < 0
.01) oocysts produced when the medium was supplemented with 10% fetal
bovine serum (FBS) and changed either daily or every other day compare
d with nor changing the medium. When the same medium was changed daily
, significantly more (P < 0.05) oocysts were produced at pH 7.4 than a
t pH 8.0 but not at pH 6.0. If the medium was changed daily, significa
ntly more (P < 0.05) oocysts were produced when medium was supplemente
d with 10% FBS only rather than 5% and 10% chicken serum. The cell-cul
ture system described in this study offers a convenient and efficient
method for investigating the biological, biochemical, and immunologica
l relationships between E. tenella and the host cell.