Toxoplasma gondii is a protozoan parasite that infects birds and mamma
ls, including humans. T. gondii T-263 is an attenuated mutant strain t
hat is being developed as a live vaccine to protect cats from shedding
oocysts. A cryopreservation procedure for T. gondii T-263 bradyzoites
has been developed to meet the requirement for product stability. A M
e(2)SO-based procedure for the cryopreservation of tachyzoites was use
d as a basis for process optimization. A modified cell culture plaque
assay was used to determine the effects of selected cryobiological par
ameters on bradyzoite viability. The major parameters evaluated were:
(i) cooling rates; (ii) intermediate plunge temperature; and (iii) tha
wing and dilution rates and temperatures. The optimized cryopreservati
on protocol comprised incubation in 12.5% Me(2)SO and 4% BSA for 30 mi
n at room temperature, cooling at 1 degrees C min(-1) to -40 degrees C
, followed by direct transfer into liquid nitrogen. Rapid thawing (app
roximately 120 degrees C min(-1)) followed by slow dilution of cryopro
tectant over 15 min resulted in the highest survival. The optimized pr
ocedure increased survival 10,000-fold over that obtained using an est
ablished tachyzoite protocol. This procedure is to be adapted for the
large-scale cryopreservation of T. gondii T-263 bradyzoites in individ
ual vaccine doses. (C) 1996 Academic Press, Inc.