# The Clinical and Laboratory Landscape of COVID-19 During the Initial Period of the Pandemic and at the Beginning of the Omicron Era

**Authors:** Yulia A. Desheva, Tamara N. Shvedova, Olga S. Kopteva, Danila S. Guzenkov, Polina A. Kudar, Tatiana S. Kotomina, Daria S. Petrachkova, Elena P. Grigorieva, Anna A. Lerner, Stanislav V. Ponkratov

PMC · DOI: 10.3390/v17040481 · 2025-03-27

## TL;DR

This study compares the clinical and immune responses of COVID-19 patients during the initial pandemic and Omicron waves, finding elevated inflammation and immune markers.

## Contribution

The study identifies Omicron-specific N protein deletions and compares immune responses across pandemic waves using HRM analysis of clinical samples.

## Key findings

- Omicron variant showed a deletion in the N protein RNA detected via HRM analysis.
- Elevated inflammatory markers and IL-6 levels were observed in both pandemic waves.
- Higher IgM and IgG antibody levels were detected during the Omicron wave, suggesting faster immune response.

## Abstract

Introduction: Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) underwent significant mutations, resulting in the Omicron variant. Methods: In this study, we analyzed blood samples from 98 patients with acute coronavirus disease 19 (COVID-19) hospitalized during the initial SARS-CoV-2 wave and the onset of Omicron in 2021. High-resolution melting (HRM) analysis of PCR products was used to analyze RNA extracted from clinical samples collected in July and November 2021 from patients infected with SARS-CoV-2. Results: HRM analysis revealed a characteristic deletion in the N protein RNA of the virus isolated in November 2021, associated with the Omicron variant. Elevated levels of inflammatory markers and interleukin-6 (IL-6) were observed in both waves of COVID-19. Complement levels and IgG and IgM antibodies to SARS-CoV-2 were detected more often during the second wave. An increase in hemagglutinin-inhibiting (HI) antibodies against influenza viruses was observed in paired blood specimens from moderate to severe COVID-19 patients during both outbreaks. Conclusions: Patients admitted during both waves of COVID-19 showed a significant rise in inflammatory markers, suggesting that Omicron triggers inflammatory responses. The rapid formation of IgM and IgG in Omicron may indicate a faster immune response. Seasonal flu may negatively impact the clinical course of coronavirus infections.

## Linked entities

- **Chemicals:** IgM (PubChem CID 71581418)
- **Diseases:** influenza (MONDO:0005812)

## Full-text entities

- **Genes:** IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}
- **Diseases:** COVID-19 (MESH:D000086382), inflammatory (MESH:D007249), flu (MESH:D007251), coronavirus infections (MESH:D018352), infected (MESH:D007239)
- **Species:** Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049], Homo sapiens (human, species) [taxon 9606], Orthomyxoviridae (family) [taxon 11308]

## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12031490/full.md

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Source: https://tomesphere.com/paper/PMC12031490