Incipient functional SARS-CoV-2 diversification identified through neural network haplotype maps

Since its introduction in the human population, SARS-CoV-2 has evolved into multiple clades, but the events in its intrahost diversification are not well understood. Here, we compare three-dimensional (3D) self-organized neural haplotype maps (SOMs) of SARS-CoV-2 from thirty individual nasopharyngea...

Descripción completa

Detalles Bibliográficos
Autores: Delgado, Soledad, Somovilla Crespo, Pilar, Ferrer-Orta, Cristina, Martínez González, Brenda, Vázquez-Monteagudo, Sergi, Muñoz-Flores, Javier, Soria, Maria Eugenia, García Crespo, Carlos, de Ávila, Ana Isabel, Durán Pastor, Antoni, Gadea Gironés, Ignacio, López Galíndez, Cecilio, Morán, Federico, Lorenzo Redondo, Ramón, Verdaguer, Nuria, Perales, Celia, Domingo, Esteban
Tipo de recurso: artículo
Fecha de publicación:2024
País:España
Institución:Universidad Autónoma de Madrid
Repositorio:Biblos-e Archivo. Repositorio Institucional de la UAM
Idioma:inglés
OAI Identifier:oai:repositorio.uam.es:10486/719033
Acceso en línea:http://hdl.handle.net/10486/719033
https://dx.doi.org/10.1073/pnas.2317851121
Access Level:acceso abierto
Palabra clave:clade transition
COVID-19
intrahost evolution
self-organized maps
viral quasispecies
Biología y Biomedicina / Biología
Descripción
Sumario:Since its introduction in the human population, SARS-CoV-2 has evolved into multiple clades, but the events in its intrahost diversification are not well understood. Here, we compare three-dimensional (3D) self-organized neural haplotype maps (SOMs) of SARS-CoV-2 from thirty individual nasopharyngeal diagnostic samples obtained within a 19-day interval in Madrid (Spain), at the time of transition between clades 19 and 20. SOMs have been trained with the haplotype repertoire present in the mutant spectra of the nsp12- and spike (S)-coding regions. Each SOM consisted of a dominant neuron (displaying the maximum frequency), surrounded by a low-frequency neuron cloud. The sequence of the master (dominant) neuron was either identical to that of the reference Wuhan-Hu-1 genome or differed from it at one nucleotide position. Six different deviant haplotype sequences were identified among the master neurons. Some of the substitutions in the neural clouds affected critical sites of the nsp12-nsp8-nsp7 polymerase complex and resulted in altered kinetics of RNA synthesis in an in vitro primer extension assay. Thus, the analysis has identified mutations that are relevant to modification of viral RNA synthesis, present in the mutant clouds of SARS-CoV-2 quasispecies. These mutations most likely occurred during intrahost diversification in several COVID-19 patients, during an initial stage of the pandemic, and within a brief time period