Production of MAG1 Antigen of Toxoplasma gondii in Escherichia coli

Authors

  • Jalal Babaie Department of Parasitology, Molecular Parasitology Laboratory, Pasteur Institute of Iran, Tehran, Iran
  • Majid Golkar Department of Parasitology, Molecular Parasitology Laboratory, Pasteur Institute of Iran, Tehran, Iran
  • Mohammad Talebzadeh Department of Parasitology, Molecular Parasitology Laboratory, Pasteur Institute of Iran, Tehran, Iran
  • Mojgan Allahyari Department of Parasitology, Molecular Parasitology Laboratory, Pasteur Institute of Iran, Tehran, Iran
  • Reyhaneh Mohabati Department of Parasitology, Molecular Parasitology Laboratory, Pasteur Institute of Iran, Tehran, Iran
  • Samira Amiri Department of Parasitology, Molecular Parasitology Laboratory, Pasteur Institute of Iran, Tehran, Iran
Abstract:

  Introduction : Toxoplasmosis is a parasitic infection caused by the protozoan Toxoplasma gondii it leads to serious medical problems in congenitally-infected and immunocompromised individuals, while it is quite harmless in immunocompetent individuals. Toxoplasma tissue cyst matrix protein (MAG1) induces early humoral and cell-mediated immune responses. Previous studies suggested recombinant MAG1 as a promising antigen for serodiagnosis of Toxoplasma infection. A DNA fragment encoding mag1, comprising amino acids 50 to 207, was amplified from T . gondii RH strain and cloned in prokaryotic expression plasmid pET-15b(+). The cloned DNA fragment was sequenced and showed 100% similarity with the published sequences available in GenBank Database. Recombinant MAG1 was expressed in Escherichia coli, and was highly purified in a single step by immobilized metal ion affinity chromatography. In Western blot analysis, purified protein showed a much stronger reactivity with sera from patients with acute Toxoplasma infection, compared to those with chronic infection. MAG1 protein, in combination with other acute-phase markers might be useful in discriminating acute/reactivated Toxoplasma infections from chronic forms. J Med Microbiol Infec Dis, 2014, 1 (2): 5 pages.

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Journal title

volume 2  issue 1

pages  40- 44

publication date 2014-01

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