Assessing the Impact of SARS-CoV-2 Lineages and Mutations on Patient Survival

More than two years into the COVID-19 pandemic, SARS-CoV-2 still remains a global public health problem. Successive waves of infection have produced new SARS-CoV-2 variants with new mutations for which the impact on COVID-19 severity and patient survival is uncertain. A total of 764 SARS-CoV-2 genom...

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Veröffentlicht in:Viruses 2022-08, Vol.14 (9), p.1893
Hauptverfasser: Loucera, Carlos, Perez-Florido, Javier, Casimiro-Soriguer, Carlos S, Ortuño, Francisco M, Carmona, Rosario, Bostelmann, Gerrit, Martínez-González, L Javier, Muñoyerro-Muñiz, Dolores, Villegas, Román, Rodriguez-Baño, Jesus, Romero-Gomez, Manuel, Lorusso, Nicola, Garcia-León, Javier, Navarro-Marí, Jose M, Camacho-Martinez, Pedro, Merino-Diaz, Laura, Salazar, Adolfo de, Viñuela, Laura, The Andalusian Covid-Sequencing Initiative, Lepe, Jose A, Garcia, Federico, Dopazo, Joaquin
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Sprache:eng
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Zusammenfassung:More than two years into the COVID-19 pandemic, SARS-CoV-2 still remains a global public health problem. Successive waves of infection have produced new SARS-CoV-2 variants with new mutations for which the impact on COVID-19 severity and patient survival is uncertain. A total of 764 SARS-CoV-2 genomes, sequenced from COVID-19 patients, hospitalized from 19th February 2020 to 30 April 2021, along with their clinical data, were used for survival analysis. A significant association of B.1.1.7, the alpha lineage, with patient mortality (log hazard ratio (LHR) = 0.51, C.I. = [0.14,0.88]) was found upon adjustment by all the covariates known to affect COVID-19 prognosis. Moreover, survival analysis of mutations in the SARS-CoV-2 genome revealed 27 of them were significantly associated with higher mortality of patients. Most of these mutations were located in the genes coding for the S, ORF8, and N proteins. This study illustrates how a combination of genomic and clinical data can provide solid evidence for the impact of viral lineage on patient survival.
ISSN:1999-4915
1999-4915
DOI:10.3390/v14091893