Hyper-Variable Spike Protein of Omicron Corona Virus and Its Differences with Alpha and Delta Variants: Prospects of RT-PCR and New Vaccine

Chakraborty Ak
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Abstract

NCBI SARS-CoV-2 Database was analyzed between November-December, 2021 to decipher the spread of Delta corona virus variants in the USA and compared with highly transmissible new omicron variant recently originated in South Africa. Presently, B.1.617.2 and AY.103 lineages Delta variants with spike protein L452R, T478K, P681R mutations and F157/R158 two amino acids deletions were predominant in the USA and superseded the deadly outbreaks of B.1.1.7 Alpha variant with deletions of H69, V70 and Y145 amino acids as well as N501Y, and D614G highly transmissible mutations. Interestingly, omicron variant has six H69, V70, V143, Y144, Y145, L212 immune-escape deletions as well as 29 mutations in the spike protein including most deadly N501Y (Y498 in omicron) and D614G (G611 in omicron). This indicated that omicron variant was originated by combination among B.1.1.7, AY.X and B.1.617.2 lineages. A unique three amino acids (EPE) insertion at 215 position of spike protein was detected to compensate six deletions suggesting further recombination events. Three Serine residues were mutated at amino acids 371 (S=L, L368 in omicron), 373 (S=P, P370 in Omicron), 375 (S=F, F372 in omicron) but compensated at 446 (G=S, S443 in omicron) and 496 (G=S, S493 in omicron) at the RBD domain of omicron virus. The three amino acids (ERS) deletion at position 30 in the N-protein acts as another signature of omicron virus. Omicron variant has less mutation in the 2/3 5’-end of the genome that codes for ORF1ab poly-protein but dominant P4715L mutation in the RNA-dependent RNA polymerase. However, overall amino acid composition, alipathic index, and instability index were found fairly constant although hydrophobic plot gave some difference between spike protein of Wuhan and omicron corona viruses. BLAST search detected 20nt and 19nt perfect match of hyper-variable 22957-22977nt region comprising 488-493 amino acids (NH2-PLRSYS-CO2H) of the spike protein of omicron virus with the ch-2 of Seladonia tumulorum or ch-16 of Steromphala cineraria respectively. A primer set designed from the RBD domain of spike gene did not detected the omicron genome by BLAST search but primers from the constant regions of the genome worked well. Such hyper-variation in the spike protein suggested that DNA vaccine or mRNA vaccine using spike gene of corona virus may not efficiently protect omicron virus infection and attenuated whole corona virus vaccine will be safer vaccine.
组粒冠病毒高变刺突蛋白及其与α和δ变异的差异:RT-PCR和新疫苗的前景
分析了2021年11月至12月NCBI SARS-CoV-2数据库,以破译Delta冠状病毒变体在美国的传播,并与最近起源于南非的高传染性新组粒变体进行了比较。目前,具有刺突蛋白L452R、T478K、P681R突变和F157/R158两个氨基酸缺失的B.1.1.7 α突变以及N501Y和D614G高传染性突变在美国占主导地位,取代了致命的爆发。有趣的是,组粒变体具有6个H69, V70, V143, Y144, Y145, L212免疫逃逸缺失以及刺突蛋白的29个突变,包括最致命的N501Y(组粒中的Y498)和D614G(组粒中的G611)。这表明组粒变异是由B.1.1.7和AY组合而成的。X和B.1.617.2血统。在刺突蛋白的215个位置检测到一个独特的3个氨基酸(EPE)插入,以弥补6个缺失,表明进一步的重组事件。三个丝氨酸残基在组粒病毒RBD结构域的371 (S=L, L368)、373 (S=P, P370)、375 (S=F, F372)氨基酸上发生突变,但在446 (G=S, S443)和496 (G=S, S493)氨基酸上得到补偿。n蛋白第30位3个氨基酸(ERS)缺失是组粒病毒的另一个特征。Omicron变体在编码ORF1ab多蛋白的基因组2/3 5 '端突变较少,但在RNA依赖的RNA聚合酶中P4715L突变占主导地位。尽管疏水性图显示武汉冠状病毒和组粒冠状病毒刺突蛋白存在一定差异,但总体氨基酸组成、脂溶性指数和不稳定性指数基本不变。BLAST搜索结果显示,组粒病毒刺突蛋白含有488 ~ 493个氨基酸(NH2-PLRSYS-CO2H)的高变量22957 ~ 22977nt区分别与黄花鸡的ch-2区和黄鸡的ch-16区有20个和19个完全匹配。从刺突基因的RBD区域设计的引物无法通过BLAST搜索检测到组粒基因组,但从基因组的恒定区域设计的引物效果良好。刺突蛋白的高度变异表明,利用冠状病毒刺突基因的DNA疫苗或mRNA疫苗可能不能有效地保护组粒病毒感染,减毒全冠病毒疫苗将是更安全的疫苗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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