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

成果类型:
Article
署名作者:
Delgado, Soledad; Somovilla, Pilar; Ferrer-Orta, Cristina; Martinez-Gonzalez, Brenda; Vazquez-Monteagudo, Sergi; Munoz-Flores, Javier; Soria, Maria Eugenia; Garcia-Crespo, Carlos; de Avila, Ana Isabel; Duran-Pastor, Antoni; Gadea, Ignacio; Lopez-Galindez, Cecilio; Moran, Federico; Lorenzo-Redondo, Ramon; Verdaguer, Nuria; Perales, Celia; Domingo, Esteban
署名单位:
Universidad Politecnica de Madrid; Consejo Superior de Investigaciones Cientificas (CSIC); CSIC - Centro de Biologia Molecular Severo Ochoa (CBM); Autonomous University of Madrid; Consejo Superior de Investigaciones Cientificas (CSIC); CSIC - Instituto de Biologia Molecular de Barcelona (IBMB); Consejo Superior de Investigaciones Cientificas (CSIC); CSIC - Centro Nacional de Biotecnologia (CNB); Autonomous University of Madrid; Instituto de Salud Carlos III; Centro Nacional de Microbiologia (CNM); Complutense University of Madrid; Northwestern University; Feinberg School of Medicine
刊物名称:
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
ISSN/ISSBN:
0027-14939
DOI:
10.1073/pnas.2317851121
发表日期:
2024-03-05
关键词:
sars-associated coronavirus spike exoribonuclease replication mutations accurate FIDELITY Covid-19
摘要:
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.