Method for detecting syphilis using synthetic antigens
An antigen and composition technology, applied in the fields of microbiology and immunology, can solve the problems of time-consuming, expensive and other problems that cannot be used as a test to detect the success of antibiotic treatment
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Embodiment 1
[0058] Embodiment 1 prepares synthetic cardiolipin and lecithin composition
[0059] Tetramyristoyl cardiolipin purified by silica gel chromatography to approximately 99% purity was obtained from Avanti Polar Lipids (Alabaster, AL) in powder form. Final concentrations of sodium salt solutions were tested for purity by TLC and HPLC. Samples were stored at -20°C. The tetramyristoyl cardiolipin was originally synthesized from semi-synthetic lipid precursors of plant origin.
[0060] Lecithin (1-palmitoyl-2-oleoyl-sn-glycerol-phosphocholine) was also obtained from Avanti Polar Lipids, purified by silica gel chromatography to about 99% purity. The lecithin was originally isolated from soybean.
[0061] A 1.2% solution of cholesterol (Avanti Polar Lipids) in absolute ethanol was prepared and filtered through alcohol rinsed filter paper #560. The cholesterol was originally obtained from lanolin and purified by recrystallization, and the crystals were stored at -20°C.
[0062] Sy...
Embodiment 2
[0063] The comparative analysis of the synthetic VDRL slide measurement and conventional VDRL slide measurement of embodiment 2
[0064] The sensitivity of the VDRL slide assay using the synthetic cardiolipin and lecithin compositions described in Example 1 was compared with A Manual of Tests for Syphilis (9th Edition, 159-77, Larsen, S.A., Pope, V., Johnson, R.E. and Kennedy, E.J.Jr. (eds.), American Public Health Association, Washington, DC) compared the sensitivity of conventional VDRL slide assays. Briefly, 0.4 ml of VDRL buffered saline (formaldehyde, Na 2 HPO 4 、KH 2 PO 4 , NaCl and distilled water) were added to the bottom of a 30 ml round bottom flask with a glass stopper or a 25 ml Erlenmeyer flask with a flat inner bottom surface. Then, 0.5 ml of the antigen composition suspension was directly added to the saline solution at a speed of 6 seconds per 0.5 ml of the antigen suspension while continuously rotating the flask. Rotation was continued for 10 seconds unti...
Embodiment 6
[0085] Comparative Analysis of Synthetic and Natural VDRL Antigens in Biological False Positive Samples (Qualitative Test)
[0086] Samples were obtained from 50 individuals originally classified as Biological False Positives (BFPs). These individuals were reactive in the non-treponemal test and non-reactive in the treponemal test. These samples were tested using the procedure of Example 3. The results of this test are listed in Table 7. Four serum samples initially misclassified as BFP were found to be reactive when assayed using CDC synthetic VDRL antigen, TP-PA and FTA-ABS. Three of these four samples were also reactive with native VDRL antigens.
[0087] Sample reactivity
[0088] R = Reactive; N = Non-reactive
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