Lawrence Livermore National Laboratory, Livermore, CA, USA.
PLoS One. 2013;8(1):e52752. doi: 10.1371/journal.pone.0052752. Epub 2013 Jan 7.
The high mutation rate of RNA viruses enables a diverse genetic population of viral genotypes to exist within a single infected host. In-host genetic diversity could better position the virus population to respond and adapt to a diverse array of selective pressures such as host-switching events. Multiple new coronaviruses, including SARS, have been identified in human samples just within the last ten years, demonstrating the potential of coronaviruses as emergent human pathogens. Deep sequencing was used to characterize genomic changes in coronavirus quasispecies during simulated host-switching. Three bovine nasal samples infected with bovine coronavirus were used to infect human and bovine macrophage and lung cell lines. The virus reproduced relatively well in macrophages, but the lung cell lines were not infected efficiently enough to allow passage of non lab-adapted samples. Approximately 12 kb of the genome was amplified before and after passage and sequenced at average coverages of nearly 950×(454 sequencing) and 38,000×(Illumina). The consensus sequence of many of the passaged samples had a 12 nucleotide insert in the consensus sequence of the spike gene, and multiple point mutations were associated with the presence of the insert. Deep sequencing revealed that the insert was present but very rare in the unpassaged samples and could quickly shift to dominate the population when placed in a different environment. The insert coded for three arginine residues, occurred in a region associated with fusion entry into host cells, and may allow infection of new cell types via heparin sulfate binding. Analysis of the deep sequencing data indicated that two distinct genotypes circulated at different frequency levels in each sample, and support the hypothesis that the mutations present in passaged strains were "selected" from a pre-existing pool rather than through de novo mutation and subsequent population fixation.
RNA 病毒的高突变率使病毒种群的多种遗传基因型存在于单个受感染的宿主中。在宿主内的遗传多样性可以使病毒种群更好地应对和适应多种选择压力,如宿主转换事件。在过去的十年中,仅从人类样本中就发现了多种新的冠状病毒,包括 SARS,这表明冠状病毒有可能成为新出现的人类病原体。深度测序用于模拟宿主转换过程中冠状病毒准种的基因组变化特征。用感染牛冠状病毒的三个牛鼻样本感染人源和牛源巨噬细胞和肺细胞系。病毒在巨噬细胞中繁殖相对较好,但肺细胞系的感染效率不够高,无法允许非实验室适应的样本通过。在传代前后,大约扩增了 12kb 的基因组,并使用 454 测序平均覆盖率接近 950×和 Illumina 测序平均覆盖率 38000×进行测序。许多传代样本的共识序列在刺突基因的共识序列中有 12 个核苷酸的插入,并且与插入的存在相关的多个点突变。深度测序显示,插入在未传代样本中存在但非常罕见,当置于不同环境中时,它可以迅速占据优势种群。该插入编码三个精氨酸残基,发生在与融合进入宿主细胞相关的区域,并且可能通过与肝素硫酸盐结合允许感染新的细胞类型。深度测序数据分析表明,在每个样本中,两种不同的基因型以不同的频率水平循环,这支持了这样一种假设,即在传代菌株中存在的突变是从预先存在的群体中“选择”出来的,而不是通过从头突变和随后的群体固定。