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Early mutational signatures and transmissibility of SARS-CoV-2 Gamma and Lambda variants in Chile.
Oróstica, Karen Y; Mohr, Sebastian B; Dehning, Jonas; Bauer, Simon; Medina-Ortiz, David; Iftekhar, Emil N; Mujica, Karen; Covarrubias, Paulo C; Ulloa, Soledad; Castillo, Andrés E; Daza-Sánchez, Anamaría; Verdugo, Ricardo A; Fernández, Jorge; Olivera-Nappa, Álvaro; Priesemann, Viola; Contreras, Seba.
  • Oróstica KY; Facultad de Medicina, Universidad de Talca, Talca, Chile.
  • Mohr SB; Max Planck Institute for Dynamics and Self-Organization, Göttingen, Germany.
  • Dehning J; Institute for the Dynamics of Complex Systems, University of Göttingen, Göttingen, Germany.
  • Bauer S; Max Planck Institute for Dynamics and Self-Organization, Göttingen, Germany.
  • Medina-Ortiz D; Institute for the Dynamics of Complex Systems, University of Göttingen, Göttingen, Germany.
  • Iftekhar EN; Max Planck Institute for Dynamics and Self-Organization, Göttingen, Germany.
  • Mujica K; Departamento de Ingeniería en Computación, Universidad de Magallanes, Punta Arenas, Chile.
  • Covarrubias PC; Max Planck Institute for Dynamics and Self-Organization, Göttingen, Germany.
  • Ulloa S; Institute for the Dynamics of Complex Systems, University of Göttingen, Göttingen, Germany.
  • Castillo AE; Sub Department of Molecular Genetics, Institute of Public Health of Chile (ISP), Santiago, Chile.
  • Daza-Sánchez A; Sub Department of Molecular Genetics, Institute of Public Health of Chile (ISP), Santiago, Chile.
  • Verdugo RA; Sub Department of Molecular Genetics, Institute of Public Health of Chile (ISP), Santiago, Chile.
  • Fernández J; Sub Department of Molecular Genetics, Institute of Public Health of Chile (ISP), Santiago, Chile.
  • Olivera-Nappa Á; Centre for Biotechnology and Bioengineering, Universidad de Chile, Santiago, Chile.
  • Priesemann V; Facultad de Medicina, Universidad de Talca, Talca, Chile.
  • Contreras S; Departamento de Oncología Básico-Clínica, Facultad de Medicina, Universidad de Chile, Santiago, Chile.
Sci Rep ; 14(1): 16000, 2024 Jul 11.
Article en En | MEDLINE | ID: mdl-38987406
ABSTRACT
Genomic surveillance (GS) programmes were crucial in identifying and quantifying the mutating patterns of SARS-CoV-2 during the COVID-19 pandemic. In this work, we develop a Bayesian framework to quantify the relative transmissibility of different variants tailored for regions with limited GS. We use it to study the relative transmissibility of SARS-CoV-2 variants in Chile. Among the 3443 SARS-CoV-2 genomes collected between January and June 2021, where sampling was designed to be representative, the Gamma (P.1), Lambda (C.37), Alpha (B.1.1.7), B.1.1.348, and B.1.1 lineages were predominant. We found that Lambda and Gamma variants' reproduction numbers were 5% (95% CI [1%, 14%]) and 16% (95% CI [11%, 21%]) larger than Alpha's, respectively. Besides, we observed a systematic mutation enrichment in the Spike gene for all circulating variants, which strongly correlated with variants' transmissibility during the studied period (r = 0.93, p-value = 0.025). We also characterised the mutational signatures of local samples and their evolution over time and with the progress of vaccination, comparing them with those of samples collected in other regions worldwide. Altogether, our work provides a reliable method for quantifying variant transmissibility under subsampling and emphasises the importance of continuous genomic surveillance.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Teorema de Bayes / SARS-CoV-2 / COVID-19 / Mutación Límite: Humans País como asunto: America do sul / Chile Idioma: En Año: 2024 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Teorema de Bayes / SARS-CoV-2 / COVID-19 / Mutación Límite: Humans País como asunto: America do sul / Chile Idioma: En Año: 2024 Tipo del documento: Article