Designing and Expression of Recombinant Chimeric Spike Protein from SARS-CoV-2 in Escherichia coli and Its Immunogenicity Assessment

IF 1.8 4区 医学 Q3 PHARMACOLOGY & PHARMACY
Sahar Karimi, Shahram Nazarian, Fattah Sotoodehnejadnematalahi, Roohollah Dorostkar, Jafar Amani
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Abstract

: Since December 2019, the world has been grappling with an ongoing global COVID-19 pandemic. Various virus variants have emerged over the past two years, each posing a greater threat than its predecessors. The recent appearance of the omicron variant (B.1.1.529) has raised significant alarm within the field of epidemiology due to its highly contagious nature and rapid transmission rate. The omicron variant possessed mutations in the key receptor-binding domain (RBD) region, the S region, and these modifications have shown a notable impact on the strain's susceptibility to neutralizing antibodies. Developing safe and efficient vaccines to prevent a future severe acute respiratory outbreak of coronavirus syndrome 2 (SARS-CoV-2) is significant. Viral surface spike proteins are ideal targets for vaccines. This study aimed to find a multi-subunit chimeric vaccine. After conducting bioinformatics analysis, the recombinant spike (RS) protein of SARS-CoV-2 was deliberately designed and subsequently produced using E. coli expression systems. The immunogenicity of RS and neutralizing antibody responses were evaluated on immunized BALB/c mice. There was a significant difference in antibody titers between RS-immunized mice and control groups. The endpoint of the serum antibody titer of mice immunized with our chimeric protein was 2.5 times higher than that of the negative control. The chimeric construct could present multiple antigens simultaneously, influentially affecting immunization. Sera from mice vaccinated by RS could recognize the SARS-CoV-2 virus and neutralize antibodies. Our chimeric peptide could bind to antibodies in the serum of patients infected with different serotypes of the SARS-CoV-2 virus, such as alpha, delta, and omicron variants. The results indicated that the RS protein would be a potential novel antigenic candidate for subunit vaccine development and could be used as a useful alternative to generate diagnostic serological tests for SARS-CoV-2 infection.
重组SARS-CoV-2嵌合刺突蛋白在大肠杆菌中的设计表达及其免疫原性评价
自2019年12月以来,世界一直在努力应对持续的全球COVID-19大流行。在过去两年中出现了各种各样的病毒变种,每一种病毒都比前一种病毒构成更大的威胁。最近出现的组粒变异(B.1.1.529)由于其高度传染性和快速传播率,在流行病学领域引起了重大警报。该组粒变体在关键受体结合域(RBD)区域S区发生突变,这些修饰对该菌株对中和抗体的易感性有显著影响。开发安全有效的疫苗以预防未来冠状病毒综合征2 (SARS-CoV-2)的严重急性呼吸道暴发具有重要意义。病毒表面刺突蛋白是疫苗的理想靶点。本研究旨在寻找一种多亚基嵌合疫苗。经过生物信息学分析,我们设计了SARS-CoV-2的重组刺突蛋白(RS),并利用大肠杆菌表达系统进行了生产。在免疫BALB/c小鼠上评价RS的免疫原性和中和抗体反应。rs免疫小鼠的抗体滴度与对照组有显著差异。用我们的嵌合蛋白免疫小鼠的终点血清抗体滴度比阴性对照高2.5倍。嵌合结构可同时呈递多种抗原,影响免疫。经RS疫苗接种的小鼠血清能够识别SARS-CoV-2病毒并中和抗体。我们的嵌合肽可以与感染不同血清型SARS-CoV-2病毒(如α、δ和组粒变体)的患者血清中的抗体结合。结果表明,RS蛋白可能是开发亚单位疫苗的一个潜在的新抗原候选物,并可作为产生SARS-CoV-2感染诊断血清学检测的有用替代方法。
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来源期刊
CiteScore
3.40
自引率
6.20%
发文量
52
审稿时长
2 months
期刊介绍: The Iranian Journal of Pharmaceutical Research (IJPR) is a peer-reviewed multi-disciplinary pharmaceutical publication, scheduled to appear quarterly and serve as a means for scientific information exchange in the international pharmaceutical forum. Specific scientific topics of interest to the journal include, but are not limited to: pharmaceutics, industrial pharmacy, pharmacognosy, toxicology, medicinal chemistry, novel analytical methods for drug characterization, computational and modeling approaches to drug design, bio-medical experience, clinical investigation, rational drug prescribing, pharmacoeconomics, biotechnology, nanotechnology, biopharmaceutics and physical pharmacy.
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