Lack of specificity of some commercial antiglobulin conjugates in indirect immunofluorescence tests

A tissue culture system that employed chick embryo fibroblasts was described for plaquing of the obligate intracellular parasite Toxoplasma gondii. High plaquing efficiency and reproducibility were accomplished by the use of secondary rather than primary cultures and the use of toxoplasma obtained from disrupted peritoneal cells of mice infected 48 hr earlier. The monolayers were cultured in a special medium which maintained the fibroblasts until the maximal number of plaques was produced. Optimal plaque formation was obtained in 5 days, and the plaques were easily counted macroscopically.