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The feasibility of automating the decision-making tasks of the medical technician in the determination of the results of the indirect fluorescent-antibody test for toxoplasmosis was investigated. Two approaches were studied: (i) macroscopic measurement of fluorescence from a large number of organisms (full-field illumination measurements), and (ii) microscopic measurements of fluorescence and morphology of individual parasites (pattern recognition). The macroscopic approach was studied utilizing an argon-ion laser in incident illumination with a Leitz Ortholux microscope and a phototube mounted so as to measure green fluorescence. Due to similar amounts of fluorescence from negative polar reactions and positive rim reactions, the macroscopic technique was concluded to be not feasible. The microscopic approach was studied utilizing a high resolution optical pattern recognition instrument. The results indicate that an object area measurement is sufficient to distinguish the presence ofToxoplasma gondii organisms from debris and overlapping organisms when studying the red fluorescence (due to Evans blue counterstain). Dark reactions were determined by the absence of green fluorescence. The differentiation of the rim and polar reactions was determined by the measurement of the ratio of green fluorescing area (due to fluorescein isothiocyanate) to red fluorescing area on the same organism. Clinically important titer information was also demonstrated to be obtainable. It was concluded that complete automation of the indirect fluorescent antibody test for toxoplasmosis is feasible with existing technology.

Automation of the Indirect Fluorescent-Antibody Test for Toxoplasmosis