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严重急性呼吸综合征冠状病毒2(SARS-CoV-2)的长期连续传代揭示了趋同进化的特征。

Long-term serial passaging of SARS-CoV-2 reveals signatures of convergent evolution.

作者信息

Foster Charles S P, Walker Gregory J, Jean Tyra, Wong Maureen, Brassil Levent, Isaacs Sonia R, Lyu Yonghui, Turville Stuart, Kelleher Anthony, Rawlinson William D

机构信息

Serology and Virology Division (SAViD), NSW Health Pathology, Prince of Wales Hospital, Sydney, New South Wales, Australia.

School of Biomedical Sciences, Faculty of Medicine and Health, University of New South Wales, Sydney, New South Wales, Australia.

出版信息

J Virol. 2025 Jul 22;99(7):e0036325. doi: 10.1128/jvi.00363-25. Epub 2025 Jun 9.

Abstract

Understanding viral evolutionary dynamics is crucial to pandemic responses, prediction of virus adaptation over time, and virus surveillance for public health strategies. Whole-genome sequencing (WGS) of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has enabled fine-grained studies of virus evolution in the human population. Serial passaging offers a complementary controlled environment to investigate the emergence and persistence of genetic variants that may confer selective advantage. In this study, nine virus lineages, including four "variants of concern" and three former "variants under investigation," were sampled over ≥33 serial passages (range 33-100) in Vero E6 cells. WGS was used to examine virus evolutionary dynamics and identify key mutations with implications for fitness and/or transmissibility. Viruses accumulated mutations regularly during serial passaging. Many low-frequency variants were lost, but others became fixed, suggesting either benefits or at least a lack of deleterious effect. Mutations arose convergently both across passage lines and when compared with contemporaneous SARS-CoV-2 clinical sequences. These mutations included some that are hypothesized to drive lineage success through host immune evasion (e.g., S:A67V, S:H655Y). The appearance of these mutations suggested key mutations can arise convergently even in the absence of a multicellular host immune response through mechanisms other than immune-driven mutation. Such mutations may provide other benefits to the viruses , or arise stochastically. Our quantitative investigation into SARS-CoV-2 evolutionary dynamics spans the greatest number of serial passages to date and will inform measures to reduce the effects of SARS-CoV-2 infection on the human population.IMPORTANCEThe ongoing evolution of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) remains a challenge for long-term public health efforts to minimize the effects of coronavirus disease 2019. Whole-genome sequencing of outbreak cases has enabled global contact tracing efforts and the identification of mutations of concern within the virus' genome. However, complementary approaches are necessary to inform our understanding of virus evolution and clinical outcomes. Here, we charted the evolution of the virus within a controlled cell culture environment, focusing on nine different virus lineages. Our approach demonstrates how SARS-CoV-2 continues to evolve readily , with changes mirroring those seen in outbreak cases globally. Findings of the study are important for (i) investigating the mechanisms of how mutations arise, (ii) predicting the future evolutionary trajectory of SARS-CoV-2, and (iii) informing treatment and prevention design.

摘要

了解病毒进化动态对于应对大流行、预测病毒随时间的适应性以及为公共卫生策略进行病毒监测至关重要。严重急性呼吸综合征冠状病毒2(SARS-CoV-2)的全基因组测序(WGS)使人们能够对人群中的病毒进化进行细粒度研究。连续传代提供了一个互补的可控环境,以研究可能赋予选择优势的遗传变异的出现和持续存在。在本研究中,对包括四种“关注变体”和三种以前的“正在调查的变体”在内的九个病毒谱系在Vero E6细胞中进行了≥33次连续传代(范围为33 - 100)的采样。使用WGS来检查病毒进化动态,并识别对适应性和/或传播性有影响的关键突变。病毒在连续传代过程中定期积累突变。许多低频变异消失了,但其他变异固定下来,这表明它们要么有益,要么至少没有有害影响。这些突变在传代谱系之间以及与同期SARS-CoV-2临床序列比较时都有趋同出现。这些突变包括一些据推测通过逃避宿主免疫来推动谱系成功的突变(例如,S:A67V、S:H655Y)。这些突变的出现表明,即使在没有多细胞宿主免疫反应的情况下,关键突变也可以通过免疫驱动突变以外的机制趋同出现。此类突变可能为病毒提供其他益处,或者随机出现。我们对SARS-CoV-2进化动态的定量研究涵盖了迄今为止最多的连续传代次数,并将为减少SARS-CoV-2感染对人群影响的措施提供参考。

重要性

严重急性呼吸综合征冠状病毒2(SARS-CoV-2)的持续进化仍然是长期公共卫生努力将2019冠状病毒病影响降至最低的一项挑战。对疫情病例的全基因组测序有助于全球接触者追踪工作以及识别病毒基因组内的关注突变。然而,需要互补的方法来增进我们对病毒进化和临床结果的理解。在这里,我们描绘了病毒在可控细胞培养环境中的进化情况,重点关注九个不同的病毒谱系。我们的方法展示了SARS-CoV-2是如何持续轻易进化的,其变化反映了全球疫情病例中所见的情况。该研究结果对于(i)研究突变产生的机制、(ii)预测SARS-CoV-2未来的进化轨迹以及(iii)为治疗和预防设计提供参考都很重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/18b3/12282192/156c1926dfac/jvi.00363-25.f001.jpg

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