Taboada Blanca, Vazquez-Perez Joel Armando, Muñoz-Medina José Esteban, Ramos-Cervantes Pilar, Escalera-Zamudio Marina, Boukadida Celia, Sanchez-Flores Alejandro, Isa Pavel, Mendieta-Condado Edgar, Martínez-Orozco José A, Becerril-Vargas Eduardo, Salas-Hernández Jorge, Grande Ricardo, González-Torres Carolina, Gaytán-Cervantes Francisco Javier, Vazquez Gloria, Pulido Francisco, Araiza-Rodríguez Adnan, Garcés-Ayala Fabiola, González-Bonilla Cesar Raúl, Grajales-Muñiz Concepción, Borja-Aburto Víctor Hugo, Barrera-Badillo Gisela, López Susana, Hernández-Rivas Lucía, Perez-Padilla Rogelio, López-Martínez Irma, Ávila-Ríos Santiago, Ruiz-Palacios Guillermo, Ramírez-González José Ernesto, Arias Carlos F
Departamento de Genética del Desarrollo y Fisiología Molecular, Instituto de Biotecnología, Universidad Nacional Autónoma de México, Cuernavaca, Morelos, Mexico.
Instituto Nacional de Enfermedades Respiratorias Ismael Cosío Villegas, Mexico City, Mexico.
J Virol. 2020 Aug 31;94(18). doi: 10.1128/JVI.01056-20.
The coronavirus disease 2019 (COVID-19) pandemic has affected most countries in the world. Studying the evolution and transmission patterns in different countries is crucial to enabling implementation of effective strategies for disease control and prevention. In this work, we present the full genome sequence for 17 SARS-CoV-2 isolates corresponding to the earliest sampled cases in Mexico. Global and local phylogenomics, coupled with mutational analysis, consistently revealed that these viral sequences are distributed within 2 known lineages, severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) lineage A/G, containing mostly sequences from North America, and lineage B/S, containing mainly sequences from Europe. Based on the exposure history of the cases and on the phylogenomic analysis, we characterized 14 independent introduction events. Additionally, three cases with no travel history were identified. We found evidence that two of these cases represented local transmission cases occurring in Mexico during mid-March 2020, denoting the earliest events described for the country. Within this local transmission cluster, we also identified an H49Y amino acid change in the Spike protein. This mutation represents a homoplasy occurring independently through time and space and may function as a molecular marker to follow any further spread of these viral variants throughout the country. Our results provide a general picture of the SARS-CoV-2 variants introduced at the beginning of the outbreak in Mexico, setting the foundation for future surveillance efforts. Understanding the introduction, spread, and establishment of SARS-CoV-2 within distinct human populations as well as the evolution of the pandemics is crucial to implement effective control strategies. In this work, we report that the initial virus strains introduced in Mexico came from Europe and the United States and that the virus was circulating locally in the country as early as mid-March. We also found evidence for early local transmission of strains with a H49Y mutation in the Spike protein, which could be further used as a molecular marker to follow viral spread within the country and the region.
2019年冠状病毒病(COVID-19)大流行已经影响了世界上大多数国家。研究不同国家的病毒演变和传播模式对于实施有效的疾病控制和预防策略至关重要。在这项工作中,我们展示了与墨西哥最早采样病例相对应的17株严重急性呼吸综合征冠状病毒2(SARS-CoV-2)分离株的全基因组序列。全球和局部系统发育基因组学,结合突变分析,一致显示这些病毒序列分布在2个已知谱系中,即严重急性呼吸综合征冠状病毒2(SARS-CoV-2)谱系A/G,主要包含来自北美的序列,以及谱系B/S,主要包含来自欧洲的序列。根据病例的暴露史和系统发育基因组分析,我们确定了14次独立的引入事件。此外,还发现了3例无旅行史的病例。我们发现有证据表明,其中2例代表2020年3月中旬在墨西哥发生的本地传播病例,这是该国描述的最早事件。在这个本地传播集群中,我们还在刺突蛋白中鉴定出一个H49Y氨基酸变化。这种突变代表了一个在时间和空间上独立发生的趋同进化,可能作为一个分子标记来追踪这些病毒变体在该国的任何进一步传播。我们的结果提供了墨西哥疫情爆发初期引入的SARS-CoV-2变体的总体情况,为未来的监测工作奠定了基础。了解SARS-CoV-2在不同人群中的引入、传播和定殖以及大流行的演变对于实施有效的控制策略至关重要。在这项工作中,我们报告说,引入墨西哥的初始病毒株来自欧洲和美国,并且该病毒早在3月中旬就在该国本地传播。我们还发现了刺突蛋白中具有H49Y突变的毒株早期本地传播的证据,这可以进一步用作分子标记来追踪病毒在该国和该地区的传播。