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Designing Multi‐Epitope Subunit Vaccine Candidate for Zika Virus Utilizing In silico Tools

عنوان مقاله: Designing Multi‐Epitope Subunit Vaccine Candidate for Zika Virus Utilizing In silico Tools
شناسه ملی مقاله: JR_REMJ-10-1_002
منتشر شده در در سال 1400
مشخصات نویسندگان مقاله:

Fatemeh Shams Moattar - Department of microbiology, Faculty of Basic Siences, Lahijan Branch Islamic Azad University, Lahijan, Guilan, Iran.
Azizeh Asadzadeh - Department of biology, faculty of science, Nour Danesh institute of higher education, Meymeh, Isfahan, Iran
Maryam Heydari - Department of biology, faculty of science, Nour Danesh institute of higher education, Meymeh, Isfahan, Iran
Maryam Zamani - Department of biology, faculty of science, Nour Danesh institute of higher education, Meymeh, Isfahan, Iran
Fatemeh Esnaashari - Department of microbiology, Faculty of Basic Siences, Lahijan Branch Islamic Azad University, Lahijan, Guilan, Iran.
Fatemeh Jeldani - Department of microbiology, Faculty of Basic Siences, Lahijan Branch Islamic Azad University, Lahijan, Guilan, Iran.

خلاصه مقاله:
Background: The arboviruses Zika virus (ZIKV) is a pathogen that threatens human health. Scientists have warned that a single mutation in the mosquito-borne ZIKV could spark another major outbreak of the disease in humans. Therefore, designing a suitable vaccine for this virus seems necessary. This study aimed to predict the protective epitopes of envelope protein from the Zika virus with bioinformatics methods for multi-epitope vaccine development. Materials and Methods: Computational studies including the identification of potential B-cell and T-cell epitopes were used. For generating a multi-epitopic vaccine construct (MEVC), selected epitopes are connected by suitable linkers. To enhance protein immunogenicity, Maltosebound protein was added to the MEVC after the prediction and refinement of the ۳D structure of the designed vaccine. The binding mode of the MEVC with toll-like receptor was investigated by molecular docking technique. Finally, molecular dynamics and in silico cloning were performed for the designed vaccine. Results: This study showed that this recombinant vaccine is nontoxic, nonallergenic, and thermostable and elicits immune responses against the Zika virus. Conclusion: The computational data suggest that the MEVC has appropriate characteristics and a high-quality structure.

کلمات کلیدی:
In-silico, Zika, multi-epitopic-vaccine-construct, Virus, Immunoinformatics, Vaccine

صفحه اختصاصی مقاله و دریافت فایل کامل: https://civilica.com/doc/1881400/