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Designing a Recombinant Multi-Epitope Antigen of Echinococcus granulosus to Diagnose Human Cystic Echinococcosis
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نویسنده
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mirzapour aliyar ,seyyed tabaei javad ,bandehpour mojgan ,haghighi ali ,kazemi bahram
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منبع
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iranian journal of parasitology - 2020 - دوره : 15 - شماره : 1 - صفحه:1 -10
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چکیده
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Background: cystic echinococcosis can cause severe disease and probable death in humans. epitopes of its antigens play a key role in the sensitivity and specificity of immunodiagnostic tests. methods: epitope prediction software programs predict the most antigenic linear b-cell epitopes of agb (8 kd), ag5, and ag95. six such epitopes were predicted and connected by “gly-ser” linker and synthesized. the purity of the concentrated recombinant multi-epitope protein was assessed by 15% sds-page. overall, 186 serum samples were collected from the loghman hakim hospital and different laboratories, tehran, iran, from july 2016 to february 2017. patients infected with hepatic hydatid cysts, patients infected by other parasites and viruses, and healthy individuals were used to detect the anti-ce igg using recombinant multi-epitope protein. results: forty-one samples out of 43 cases of hydatidosis were diagnosed correctly as positive, and two were negative. in addition, six negative cases of healthy individual group were diagnosed as positive and negative with rmep-elisa and the commercial kit, respectively. therefore, these six samples were considered as false positive using our method. in addition, a diagnostic sensitivity of 95.3% (95% ci, 84.19% to 99.43%) and a specificity of 95.0% (95% ci, 89.43% to 98.14%) were obtained using optimum cutoff value (0.20). the sensitivity and specificity of the commercial kit was 100%. conclusion: our findings showed high diagnostic accuracy of the elisa test using the developed recombinant protein, which encourages the use of this recombinant multi-epitope protein for rapid serological diagnosis of hydatidosis.
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کلیدواژه
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Multi-epitope ,Echinococcus granulosus ,Hydatidosis ,ELISA
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آدرس
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shahid beheshti university of medical sciences, international branch, department of medical parasitology and mycology, Iran. islamic azad university, mashhad branch, school of medicine, department of parasitology and mycology, Iran, shahid beheshti university of medical sciences, school of medicine, department of medical parasitology and mycology, Iran, shahid beheshti university of medical sciences, school of advanced technologies in medicine, cellular and molecular biology research center, department of biotechnology, Iran, shahid beheshti university of medical sciences, school of medicine, department of medical parasitology and mycology, Iran, shahid beheshti university of medical sciences, school of medicine, school of advanced technologies in medicine, department of biotechnology, department of medical parasitology and mycology, Iran
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پست الکترونیکی
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kazemi@sbmu.ac.ir
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Authors
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