Characterization and immunogenicity assessment of MERS-CoV pre-fusion spike trimeric oligomers as vaccine immunogen

ABSTRACTMiddle East respiratory syndrome coronavirus (MERS-CoV) is a lethal beta-coronavirus that emerged in 2012. The virus is part of the WHO blueprint priority list with a concerning fatality rate of 35%. Scientific efforts are ongoing for the development of vaccines, anti-viral and biotherapeuti...

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Main Authors: Rahul Ahuja (Author), Preeti Vishwakarma (Author), Sneha Raj (Author), Varun Kumar (Author), Ritika Khatri (Author), Bharat Lohiya (Author), Shikha Saxena (Author), Gurleen Kaur (Author), Gagandeep Singh (Author), Shailendra Asthana (Author), Shubbir Ahmed (Author), Sweety Samal (Author)
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Published: Taylor & Francis Group, 2024-12-01T00:00:00Z.
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042 |a dc 
100 1 0 |a Rahul Ahuja  |e author 
700 1 0 |a Preeti Vishwakarma  |e author 
700 1 0 |a Sneha Raj  |e author 
700 1 0 |a Varun Kumar  |e author 
700 1 0 |a Ritika Khatri  |e author 
700 1 0 |a Bharat Lohiya  |e author 
700 1 0 |a Shikha Saxena  |e author 
700 1 0 |a Gurleen Kaur  |e author 
700 1 0 |a Gagandeep Singh  |e author 
700 1 0 |a Shailendra Asthana  |e author 
700 1 0 |a Shubbir Ahmed  |e author 
700 1 0 |a Sweety Samal  |e author 
245 0 0 |a Characterization and immunogenicity assessment of MERS-CoV pre-fusion spike trimeric oligomers as vaccine immunogen 
260 |b Taylor & Francis Group,   |c 2024-12-01T00:00:00Z. 
500 |a 10.1080/21645515.2024.2351664 
500 |a 2164-554X 
500 |a 2164-5515 
520 |a ABSTRACTMiddle East respiratory syndrome coronavirus (MERS-CoV) is a lethal beta-coronavirus that emerged in 2012. The virus is part of the WHO blueprint priority list with a concerning fatality rate of 35%. Scientific efforts are ongoing for the development of vaccines, anti-viral and biotherapeutics, which are majorly directed toward the structural spike protein. However, the ongoing effort is challenging due to conformational instability of the spike protein and the evasion strategy posed by the MERS-CoV. In this study, we have expressed and purified the MERS-CoV pre-fusion spike protein in the Expi293F mammalian expression system. The purified protein was extensively characterized for its biochemical and biophysical properties. Thermal stability analysis showed a melting temperature of 58°C and the protein resisted major structural changes at elevated temperature as revealed by fluorescence spectroscopy and circular dichroism. Immunological assessment of the MERS-CoV spike immunogen in BALB/c mice with AddaVaxTM and Imject alum adjuvants showed elicitation of high titer antibody responses but a more balanced Th1/Th2 response with AddaVaxTM squalene like adjuvant. Together, our results suggest the formation of higher-order trimeric pre-fusion MERS-CoV spike proteins, which were able to induce robust immune responses. The comprehensive characterization of MERS-CoV spike protein warrants a better understanding of MERS spike protein and future vaccine development efforts. 
546 |a EN 
690 |a MERS-CoV vaccine 
690 |a prefusion spike 
690 |a immunogenicity 
690 |a thermostability, antibody response 
690 |a Immunologic diseases. Allergy 
690 |a RC581-607 
690 |a Therapeutics. Pharmacology 
690 |a RM1-950 
655 7 |a article  |2 local 
786 0 |n Human Vaccines & Immunotherapeutics, Vol 20, Iss 1 (2024) 
787 0 |n https://www.tandfonline.com/doi/10.1080/21645515.2024.2351664 
787 0 |n https://doaj.org/toc/2164-5515 
787 0 |n https://doaj.org/toc/2164-554X 
856 4 1 |u https://doaj.org/article/4e44e7d9cd2b4a2bae31dfb3939ef7df  |z Connect to this object online.