production of mag1 antigen of toxoplasma gondii in escherichia coli

نویسندگان

mohammad talebzadeh 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

jalal babaie 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

چکیده

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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عنوان ژورنال:
journal of medical microbiology and infectious diseases

جلد ۲، شماره ۱، صفحات ۴۰-۴۴

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