Mutation in a SARS-CoV-2 Haplotype from Sub-Antarctic Chile Reveals New Insights into the Spike's Dynamics.
Jorge González-PuelmaJacqueline AldridgeMarco Montes de OcaMónica PintoRoberto Uribe-ParedesJosé Fernández-GoycooleaDiego Alvarez-SaraviaHermy ÁlvarezGonzalo EncinaThomas WeitzelRodrigo MuñozAlvaro Olivera-NappaSergio PantanoMarcelo A NavarretePublished in: Viruses (2021)
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.
Keyphrases
- sars cov
- escherichia coli
- respiratory syndrome coronavirus
- molecular dynamics
- pseudomonas aeruginosa
- staphylococcus aureus
- biofilm formation
- antimicrobial resistance
- public health
- binding protein
- risk assessment
- molecular dynamics simulations
- risk factors
- single cell
- coronavirus disease
- gene expression
- amino acid
- protein protein
- sensitive detection
- monte carlo