Mutation in a SARS-CoV-2 Haplotype from Sub-Antarctic Chile Reveals New Insights into the Spike’s Dynamics
Jorge González-Puelma,
Jacqueline Aldridge,
Marco Montes de Oca,
Mónica Pinto,
Roberto Uribe-Paredes,
José Fernández-Goycoolea,
Diego Alvarez-Saravia,
Hermy Álvarez,
Gonzalo Encina,
Thomas Weitzel,
Rodrigo Muñoz,
Álvaro Olivera-Nappa,
Sergio Pantano,
Marcelo A. Navarrete
Affiliations
Jorge González-Puelma
Escuela de Medicina, Universidad de Magallanes, Punta Arenas 6210427, Chile
Jacqueline Aldridge
Departamento de Ingeniería en Computación, Universidad de Magallanes, Punta Arenas 6210427, Chile
Marco Montes de Oca
Departamento de Ingeniería en Computación, Universidad de Magallanes, Punta Arenas 6210427, Chile
Mónica Pinto
Escuela de Medicina, Universidad de Magallanes, Punta Arenas 6210427, Chile
Roberto Uribe-Paredes
Departamento de Ingeniería en Computación, Universidad de Magallanes, Punta Arenas 6210427, Chile
José Fernández-Goycoolea
Departamento de Matemática y Física, Universidad de Magallanes, Punta Arenas 6210427, Chile
Diego Alvarez-Saravia
Escuela de Medicina, Universidad de Magallanes, Punta Arenas 6210427, Chile
Hermy Álvarez
Escuela de Medicina, Universidad de Magallanes, Punta Arenas 6210427, Chile
Gonzalo Encina
Centro de Genética y Genómica, Instituto de Ciencias e Innovación en Medicina, Facultad de Medicina Clínica Alemana, Universidad del Desarrollo, Santiago 7610658, Chile
Thomas Weitzel
Laboratorio Clínico, Clínica Alemana de Santiago, Facultad de Medicina Clínica Alemana, Universidad del Desarrollo, Santiago 7610658, Chile
Rodrigo Muñoz
Escuela de Medicina, Universidad de Magallanes, Punta Arenas 6210427, Chile
Álvaro Olivera-Nappa
Centre for Biotechnology and Bioengineering, Universidad de Chile, Santiago 8370456, Chile
Sergio Pantano
Biomolecular Simulations Group, Institut Pasteur de Montevideo, Montevideo 11400, Uruguay
Marcelo A. Navarrete
Escuela de Medicina, Universidad de Magallanes, Punta Arenas 6210427, Chile
The emergence of SARS-CoV-2 variants, as observed with the D614G spike protein mutant and, more recently, with B.1.1.7 (501Y.V1), B.1.351 (501Y.V2) and B.1.1.28.1 (P.1) lineages, represent a continuous threat and might lead to strains of higher infectivity and/or virulence. We report on the occurrence of a SARS-CoV-2 haplotype with nine mutations including D614G/T307I double-mutation of the spike. This variant expanded and completely replaced previous lineages within a short period in the subantarctic Magallanes Region, southern Chile. The rapid lineage shift was accompanied by a significant increase of cases, resulting in one of the highest incidence rates worldwide. Comparative coarse-grained molecular dynamic simulations indicated that T307I and D614G belong to a previously unrecognized dynamic domain, interfering with the mobility of the receptor binding domain of the spike. The T307I mutation showed a synergistic effect with the D614G. Continuous surveillance of new mutations and molecular analyses of such variations are important tools to understand the molecular mechanisms defining infectivity and virulence of current and future SARS-CoV-2 strains.