Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA.
Department of Genome Sciences, University of Washington, Seattle, WA 98195, USA.
Sci Transl Med. 2021 May 26;13(595). doi: 10.1126/scitranslmed.abf0202. Epub 2021 May 3.
The rapid spread of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has gravely affected societies around the world. Outbreaks in different parts of the globe have been shaped by repeated introductions of new viral lineages and subsequent local transmission of those lineages. Here, we sequenced 3940 SARS-CoV-2 viral genomes from Washington State (USA) to characterize how the spread of SARS-CoV-2 in Washington State in early 2020 was shaped by differences in timing of mitigation strategies across counties and by repeated introductions of viral lineages into the state. In addition, we show that the increase in frequency of a potentially more transmissible viral variant (614G) over time can potentially be explained by regional mobility differences and multiple introductions of 614G but not the other variant (614D) into the state. At an individual level, we observed evidence of higher viral loads in patients infected with the 614G variant. However, using clinical records data, we did not find any evidence that the 614G variant affects clinical severity or patient outcomes. Overall, this suggests that with regard to D614G, the behavior of individuals has been more important in shaping the course of the pandemic in Washington State than this variant of the virus.
严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)的迅速传播严重影响了世界各地的社会。全球不同地区的疫情受到新病毒谱系不断传入和随后这些谱系在当地传播的影响。在这里,我们对来自华盛顿州(美国)的 3940 个 SARS-CoV-2 病毒基因组进行了测序,以描述 SARS-CoV-2 在 2020 年初在华盛顿州的传播方式,这些方式受到不同县缓解策略实施时间的差异以及病毒谱系反复传入的影响。此外,我们还表明,随着时间的推移,一种潜在传播能力更强的病毒变体(614G)的出现频率增加,可能是由区域流动性差异和 614G 多次传入该州引起的,但不是其他变体(614D)。在个体水平上,我们观察到感染 614G 变体的患者病毒载量更高的证据。然而,使用临床记录数据,我们没有发现任何证据表明 614G 变体影响临床严重程度或患者结局。总的来说,这表明就 D614G 而言,在塑造华盛顿州大流行进程方面,个体行为比该病毒的这一变体更为重要。