SARS-CoV-2 Molecular Evolution: A Focus on Omicron Variants in Umbria, Italy.

SARS-CoV-2 Molecular Evolution: A Focus on Omicron Variants in Umbria, Italy.

Publication date: Jun 29, 2024

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has caused more than 6 million deaths worldwide, and the spread of new variants over time increased the ability of this virus to cause infection. The Omicron variant was detected for the first time in Umbria, a region of central Italy, in November 2021 and it induced an unprecedented increase in the number of infection cases. Here, we analysed 3300 SARS-CoV-2 positive samples collected in Umbria between April 2022 and December 2023. We traced the molecular evolution of SARS-CoV-2 variants over time through the Next-Generation Sequencing (NGS) approach. We assessed correlation between SARS-CoV-2 infection and patients’ health status. In total, 17. 3% of our samples came from patients hospitalised as a consequence of COVID-19 infection even though 81. 4% of them received at least three vaccine doses. We identified only Omicron variants, and the BA. 5 lineage was detected in the majority of our samples (49. 2%). Omicron variants outcompeted each other through the acquisition of mutations especially in Spike glycoprotein that are fingerprints of each variant. Viral antigenic evolution confers higher immunological escape and makes a continuous improvement of vaccine formulation necessary. The continuous update of international genomic databases with sequencing results obtained by emergent pathogens is essential to manage a possible future pandemic.

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Concepts Keywords
Coronavirus epidemiology
December molecular evolution
Hospitalised monitoring
Increased NGS sequencing
Italy Omicron variants
SARS-CoV-2

Semantics

Type Source Name
disease VO Severe acute respiratory syndrome coronavirus 2
disease VO time
disease MESH infection
disease MESH SARS-CoV-2 infection
pathway REACTOME SARS-CoV-2 Infection
disease VO vaccine
disease VO Glycoprotein
disease MESH virus infection
disease VO organization
disease VO vaccine effectiveness
drug DRUGBANK Coenzyme M
disease MESH pneumonia
drug DRUGBANK Nonoxynol-9
disease VO population
disease MESH Immunocompromised patients
pathway KEGG Viral replication
disease VO ineffective
disease MESH Influenza
disease MESH reinfections
disease VO Iss
disease VO monthly
drug DRUGBANK Dimercaprol
disease VO unvaccinated
disease VO vaccine dose
disease VO vaccination
disease IDO history
disease VO dose
disease VO immunized
disease IDO infection incidence
drug DRUGBANK Ademetionine
disease VO URE
disease IDO country
disease MESH SD1

Original Article

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