Evidence map›Paper›PMID 40806685›Full record

ArticleInternational journal of molecular sciences2025

An Italian Single-Center Genomic Surveillance Study: Two-Year Analysis of SARS-CoV-2 Spike Protein Mutations.

Riccardo Cecchetto, Emil Tonon, Asia Palmisano, Anna Lagni, Erica Diani, Virginia Lotti, Marco Mantoan, Livio Montesarchio, Francesca Palladini, Giona Turri and 1 more

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Riccardo CecchettoDepartment of Diagnostic and Public Health, Division of Microbiology, University of Verona, 37134 Verona, Italy.ORCID 0009-0000-5189-8867
Emil TononDepartment of Diagnostic and Public Health, Division of Microbiology, University of Verona, 37134 Verona, Italy.
Asia PalmisanoDepartment of Diagnostic and Public Health, Division of Microbiology, University of Verona, 37134 Verona, Italy.
Anna LagniDepartment of Diagnostic and Public Health, Division of Microbiology, University of Verona, 37134 Verona, Italy.ORCID 0009-0005-1044-3109
Erica DianiDepartment of Diagnostic and Public Health, Division of Microbiology, University of Verona, 37134 Verona, Italy.ORCID 0000-0002-1373-7533
Virginia LottiDepartment of Diagnostic and Public Health, Division of Microbiology, University of Verona, 37134 Verona, Italy.ORCID 0000-0002-5746-3810
Marco MantoanDepartment of Diagnostic and Public Health, Division of Hygiene and Preventive, Environmental and Occupational Medicine, University of Verona, 37134 Verona, Italy.ORCID 0009-0004-1856-7088
Livio MontesarchioHospital Management, University Hospital of Verona, 37126 Verona, Italy.ORCID 0009-0001-4982-4153
Francesca PalladiniHospital Management, University Hospital of Verona, 37126 Verona, Italy.
Giona TurriUOC Microbiology, AOUI Verona, 37134 Verona, Italy.
Davide GibelliniDepartment of Diagnostic and Public Health, Division of Microbiology, University of Verona, 37134 Verona, Italy.

Funding

Department of Diagnostic and Public Health, Microbiology Section, University of Verona Quota FUR Erica DianiDepartment of Diagnostic and Public Health, Microbiology Section, University of Verona Quota FUR Prof. GibelliniDepartment of Diagnostic and Public Health, Microbiology Section, University of Verona Quota FUR Virginia LottiMinistero dell'università e della ricerca Department of Excellence 2023/2027, MUR, Italy
6 · The paper itself

Abstract

The repeated occurrence of SARS-CoV-2 variants, largely driven by virus-host interactions, was and will remain a public health concern. Spike protein mutations shaped viral infectivity, transmissibility, and immune escape. From February 2022 to April 2024, a local genomic surveillance program in Verona, Italy, was conducted on 1333 SARS-CoV-2-positive nasopharyngeal swabs via next generation full-length genome sequencing. Spike protein mutations were classified based on their prevalence over time. Mutations were grouped into five categories: fixed, emerging, fading, transient, and divergent. Notably, some divergent mutations displayed a "Lazarus effect," disappearing and later reappearing in new lineages, indicating potential adaptive advantages in specific genomic contexts. This two-year surveillance study highlights the dynamic nature of spike protein mutations and their role in SARS-CoV-2 evolution. The findings underscore the need for ongoing mutation-focused genomic monitoring to detect early signals of variant emergence, especially among mutations previously considered disadvantageous. Such efforts are critical for driving public health responses and guiding future vaccine and therapeutic strategies.

Indexed as

COVID-19MutationSARS-CoV-2Spike Glycoprotein, CoronavirusAdolescentAdultAgedFemaleGenome, ViralGenomicsHumansItalyMaleMiddle AgedSpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2genomic surveillancemutational analysisSARS-CoV-2spike proteinwhole genome sequencing

Identifiers

PMID40806685
PMCPMC12347092

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.