Department of Biomedical Engineering, Tel Aviv University, Tel Aviv, Israel.
SynVaccineLtd. Ramat Hachayal, Tel Aviv, Israel.
BMC Bioinformatics. 2018 May 8;19(Suppl 6):140. doi: 10.1186/s12859-018-2132-3.
Synthetic virology is an important multidisciplinary scientific field, with emerging applications in biotechnology and medicine, aiming at developing methods to generate and engineer synthetic viruses. In particular, many of the RNA viruses, including among others the Dengue and Zika, are widespread pathogens of significant importance to human health. The ability to design and synthesize such viruses may contribute to exploring novel approaches for developing vaccines and virus based therapies.
Here we develop a full multidisciplinary pipeline for generation and analysis of synthetic RNA viruses and specifically apply it to Dengue virus serotype 2 (DENV-2). The major steps of the pipeline include comparative genomics of endogenous and synthetic viral strains. Specifically, we show that although the synthetic DENV-2 viruses were found to have lower nucleotide variability, their phenotype, as reflected in the study of the AG129 mouse model morbidity, RNA levels, and neutralization antibodies, is similar or even more pathogenic in comparison to the wildtype master strain. Additionally, the highly variable positions, identified in the analyzed DENV-2 population, were found to overlap with less conserved homologous positions in Zika virus and other Dengue serotypes. These results may suggest that synthetic DENV-2 could enhance virulence if the correct sequence is selected.
The approach reported in this study can be used to generate and analyze synthetic RNA viruses both on genotypic and on phenotypic level. It could be applied for understanding the functionality and the fitness effects of any set of mutations in viral RNA and for editing RNA viruses for various target applications.
合成病毒学是一个重要的多学科科学领域,在生物技术和医学中有新兴应用,旨在开发生成和工程合成病毒的方法。特别是,许多 RNA 病毒,包括登革热和寨卡病毒等,都是对人类健康具有重要意义的广泛存在的病原体。设计和合成此类病毒的能力可能有助于探索开发疫苗和基于病毒的治疗方法的新方法。
在这里,我们开发了一个用于生成和分析合成 RNA 病毒的完整多学科管道,并特别将其应用于登革热病毒血清型 2(DENV-2)。该管道的主要步骤包括内源性和合成病毒株的比较基因组学。具体来说,我们表明,尽管合成的 DENV-2 病毒被发现具有较低的核苷酸变异性,但它们的表型,如在 AG129 小鼠模型发病机制、RNA 水平和中和抗体研究中反映的,与野生型主株相比相似,甚至更具致病性。此外,在所分析的 DENV-2 群体中鉴定出的高度可变位置与寨卡病毒和其他登革热血清型中较少保守的同源位置重叠。这些结果可能表明,如果选择正确的序列,合成的 DENV-2 可能会增强毒力。
本研究报告的方法可用于在基因型和表型水平上生成和分析合成 RNA 病毒。它可用于了解病毒 RNA 中任何一组突变的功能和适应性影响,并用于编辑各种目标应用的 RNA 病毒。