Toxoplasma gondii is an intracellular protozoan parasite of worldwide distr
ibution. Parasites that habour a complete antigenic profile, that is necess
ary for the serological diagnosis of human Toxoplasma infections, are provi
ded by in vivo culture methods only. It seems that the host immune pressure
is responsible for the expression of a total antigen pattern. Thus, in mos
t laboratories the asexual proliferative stage of the parasite, the tachyzo
ite, is maintained by successive intraperitoneal passages in highly suscept
ible animals such as mice.
We would like to develop an in vitro method to provide sufficient amounts o
f high quality parasite antigen suitable for diagnosis of Toxoplasmosis. Us
ing the RAPD-PCR (random amplified polymorphic DNA-PCR) technique, we were
able to show that during different culture conditions (in vivo and in vitro
culture) the parasites undergo no clonal selection. That means the entire
parasite population changes the protein expression pattern clue to the in v
itro culture conditions. Based on the result described previously the work
could be continued as follows. One strategy could be to simulate the host i
mmune pressure during the in vitro cultivation of the tachyzoites. A more c
onvinced approach may be the production of recombinant parasite antigens us
eful for diagnosis of a Toxoplasma infection in human adults and newborns.