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Toxoplasma gondii excretory secretory antigenic proteins of diagnostic potential
Author(s) -
SAADATNIA GEITA,
MOHAMED ZEEHAIDA,
GHAFFARIFAR FATEMEH,
OSMAN EMELIA,
MOGHADAM ZOHREH KAZEMI,
NOORDIN RAHMAH
Publication year - 2012
Publication title -
apmis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.909
H-Index - 88
eISSN - 1600-0463
pISSN - 0903-4641
DOI - 10.1111/j.1600-0463.2011.02810.x
Subject(s) - toxoplasma gondii , blot , antigen , phosphoglycerate mutase , toxoplasmosis , biology , western blot , antibody , microbiology and biotechnology , molecular mass , immunology , virology , enzyme , biochemistry , glycolysis , gene
Saadatnia G, Mohamed Z, Ghaffarifar F, Osman E, Kazemi Moghadam Z, Noordin R. Toxoplasma gondii excretory secretory antigenic proteins of diagnostic potential. APMIS 2012; 120: 47–55. Infection with Toxoplasma gondii is widespread and important in humans, especially pregnant women and immunosuppressed patients. A panel of tests is usually required for diagnosis toxoplasmosis. Excretory secretory antigen (ESA) is highly immunogenic, and thus it is a good candidate for investigation into new infection markers. ESA was prepared from tachyzoites of RH strain of T. gondii by mice intraperitoneal infection. Sera were obtained from several categories of individuals who differed in their status of anti‐ Toxoplasma IgM, IgG and IgG avidity antibodies. The ESA was subjected to SDS‐PAGE, two‐dimensional gel electrophoresis and Western blot analysis. Antigenic bands of approximate molecular weights of 12, 20 and 30 kDa, when probed with anti‐human IgM‐HRP and IgA‐HRP, showed good potential as infection markers. The highest sensitivity of the bands was 98.7% with combination of IgM and IgA blots with sera of patients with anti‐ Toxoplasma IgM+ IgG+. The specificities were 84% and 70% with sera from other infections and healthy controls in IgM blots and IgA blots respectively. By mass spectrometry, the 12 kDa protein was identified as thioredoxin. The two top proteins identified for 20 kDa molecule were microneme protein 10 and dense granule protein 7; whereas that for 30 kDa were phosphoglycerate mutase 1 and phosphoglycerate mutase.