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Identification of Toxoplasma gondii SUB1 antigen as a marker for acute infection by use of an innovative evaluation method.
- Source :
-
Journal of clinical microbiology [J Clin Microbiol] 2011 Jul; Vol. 49 (7), pp. 2419-25. Date of Electronic Publication: 2011 May 04. - Publication Year :
- 2011
-
Abstract
- By the separation of Toxoplasma lysate using two-dimensional gel electrophoresis and its analysis with human serum samples and mass spectrometry, the subtilisin-like protein (SUB1) was identified to be a potential marker for acute toxoplasmosis. Following expression of the C-terminal domain of SUB1 in Escherichia coli, it was tested in a line blot assay using a total of 80 human serum samples. Two computer programs based on different evaluation strategies were used for judgment of the line blot results: (i) a time-dependent method with a predefined cutoff value and (ii) a fixed-time-point method with a calculated cutoff. Thereby, SUB1 was proven to be rather reactive with specific immunoglobulin A (IgA), IgM, and IgG of patients with an acute infection. This finding makes this antigen an attractive candidate for improving diagnosis of toxoplasmosis and demonstrates that not only the selection of respective antigens but also the evaluation method chosen are important for the evaluation of new diagnostic markers.
- Subjects :
- Clinical Laboratory Techniques methods
Electrophoresis, Gel, Two-Dimensional
Humans
Immunoassay methods
Immunoglobulin A blood
Immunoglobulin G blood
Immunoglobulin M blood
Mass Spectrometry
Parasitology methods
Proteome analysis
Sensitivity and Specificity
Toxoplasma chemistry
Antibodies, Protozoan blood
Antigens, Protozoan immunology
Biomarkers blood
Protozoan Proteins analysis
Protozoan Proteins immunology
Subtilisins immunology
Toxoplasma immunology
Toxoplasmosis diagnosis
Subjects
Details
- Language :
- English
- ISSN :
- 1098-660X
- Volume :
- 49
- Issue :
- 7
- Database :
- MEDLINE
- Journal :
- Journal of clinical microbiology
- Publication Type :
- Academic Journal
- Accession number :
- 21543561
- Full Text :
- https://doi.org/10.1128/JCM.00464-11