Evidence map›Paper›PMID 42616572›Full record

ArticleThe Journal of general virology2026

Dose-dependent effects of recombinant spike protein-based vaccination on SARS-CoV-2 evolutionary dynamics and the emergence of variants in hamster models.

Kyuyoung Shim, Jeong Hwa Choi, Eun-Ha Hwang, Green Kim, Gyu-Seo Bae, Eunsu Jeon, Seung Ho Baek, Hee-Sung Kim, Seok Hwan Kim, Dae-Soo Kim and 3 more

Abstract read
In one paragraph

Article in The Journal of general virology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

13 authors.

Kyuyoung ShimKorea Research Institute of Bioscience and Biotechnology, Cheongju, Republic of Korea.
Jeong Hwa ChoiKorea Research Institute of Bioscience and Biotechnology, Cheongju, Republic of Korea.
Eun-Ha HwangKorea Research Institute of Bioscience and Biotechnology, Cheongju, Republic of Korea.
Green KimKorea Research Institute of Bioscience and Biotechnology, Cheongju, Republic of Korea.
Gyu-Seo BaeKorea Research Institute of Bioscience and Biotechnology, Cheongju, Republic of Korea.
Eunsu JeonKorea Research Institute of Bioscience and Biotechnology, Cheongju, Republic of Korea.
Seung Ho BaekKorea Research Institute of Bioscience and Biotechnology, Cheongju, Republic of Korea.
Hee-Sung KimCollege of Medicine, Chungbuk National University, Cheongju, Republic of Korea.
Seok Hwan KimCollege of Medicine, Chungnam National University, Daejeon, Republic of Korea.
Dae-Soo KimKorea Research Institute of Bioscience and Biotechnology, Cheongju, Republic of Korea.
Kiwon JangKorea Research Institute of Bioscience and Biotechnology, Cheongju, Republic of Korea.
Jung Joo HongKorea Research Institute of Bioscience and Biotechnology, Cheongju, Republic of Korea.
Bon-Sang KooKorea Research Institute of Bioscience and Biotechnology, Cheongju, Republic of Korea.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has continued to circulate globally through the persistent emergence of novel variants. Vaccination has been regarded as one of the selective environments that can influence SARS-CoV-2 evolution by exerting immune pressure. This study investigated the evolutionary dynamics of the SARS-CoV-2 Delta variant in hamsters immunized with varying doses of a full-length spike protein vaccine, potentially reflecting the heterogeneous levels of immunity. In hamster models, higher vaccine doses prevented viral replication in the lungs but only partially suppressed replication in the nasal passages. After excluding intra-host single-nucleotide variants (iSNVs) detected in non-vaccinated controls, a negative binomial model adjusting for read depth revealed a significant vaccine dose-dependent increase in iSNV occurrence in the Spike, ORF1a, ORF1b and ORF3a genes in nasal samples and positive selection signals were predominantly observed in the highest vaccine dose group. The iSNVs were observed in diverse and distinct combinations that were unique to each individual, reflecting host-specific intra-host mutation patterns. Some aa substitutions detected in at least two individuals in the vaccinated group were more frequently observed in the Omicron variant.

Indexed as

COVID-19COVID-19 VaccinesSARS-CoV-2Spike Glycoprotein, CoronavirusAnimalsAntibodies, NeutralizingAntibodies, ViralCricetinaeDisease Models, AnimalDose-Response Relationship, ImmunologicEvolution, MolecularHumansLungMesocricetusVaccinationVirus ReplicationAntibodies, NeutralizingAntibodies, ViralCOVID-19 VaccinesSpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2delta variantintra-host single-nucleotide variantsOmicron variantSARS-CoV-2viral evolution

Identifiers

PMID42616572
PMCPMC13489668

What OpenQuestion holds

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Registered trials

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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.