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SARS-CoV-2 密码子的优化和去优化及其对疫苗开发的相关影响。

Optimization and Deoptimization of Codons in SARS-CoV-2 and Related Implications for Vaccine Development.

机构信息

State Key Laboratory of Protein and Plant Gene Research, Center for Bioinformatics, School of Life Sciences, Peking University, Beijing, 100871, China.

NHC Key Laboratory of Systems Biology of Pathogens, Institute of Pathogen Biology, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100176, China.

出版信息

Adv Sci (Weinh). 2023 Aug;10(23):e2205445. doi: 10.1002/advs.202205445. Epub 2023 Jun 2.

Abstract

The spread of coronavirus disease 2019 (COVID-19), caused by severe respiratory syndrome coronavirus 2 (SARS-CoV-2), has progressed into a global pandemic. To date, thousands of genetic variants have been identified among SARS-CoV-2 isolates collected from patients. Sequence analysis reveals that the codon adaptation index (CAI) values of viral sequences have decreased over time but with occasional fluctuations. Through evolution modeling, it is found that this phenomenon may result from the virus's mutation preference during transmission. Using dual-luciferase assays, it is further discovered that the deoptimization of codons in the viral sequence may weaken protein expression during virus evolution, indicating that codon usage may play an important role in virus fitness. Finally, given the importance of codon usage in protein expression and particularly for mRNA vaccines, it is designed several codon-optimized Omicron BA.2.12.1, BA.4/5, and XBB.1.5 spike mRNA vaccine candidates and experimentally validated their high levels of expression. This study highlights the importance of codon usage in virus evolution and provides guidelines for codon optimization in mRNA and DNA vaccine development.

摘要

新型冠状病毒病 2019(COVID-19)由严重急性呼吸系统综合征冠状病毒 2(SARS-CoV-2)引起,已进展为全球大流行。迄今为止,已从患者中采集的 SARS-CoV-2 分离物中鉴定出数千种遗传变异。序列分析表明,病毒序列的密码子适应指数(CAI)值随时间降低,但偶尔会波动。通过进化建模发现,这种现象可能是由于病毒在传播过程中的突变偏好所致。通过双荧光素酶检测,进一步发现病毒序列中密码子的去优化可能会削弱病毒进化过程中的蛋白表达,表明密码子使用可能在病毒适应性中起重要作用。最后,鉴于密码子使用在蛋白表达中的重要性,特别是对于 mRNA 疫苗,设计了几种密码子优化的 Omicron BA.2.12.1、BA.4/5 和 XBB.1.5 刺突 mRNA 疫苗候选物,并通过实验验证了它们的高水平表达。本研究强调了密码子使用在病毒进化中的重要性,并为 mRNA 和 DNA 疫苗开发中的密码子优化提供了指导。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/62d3/10427376/a850153b96a7/ADVS-10-2205445-g003.jpg

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