Evidence map›Paper›PMID 41262874›Full record

ArticleFrontiers in cellular and infection microbiology2025

Novel method for the identification of circulating SARS-CoV-2 variants and clinical characteristics of patient infection with SARS-CoV-2 variants in Central China.

Youhua Yuan, Yiman Geng, Tingjun Rong, Baoya Wang, Xiaohuan Mao, Xiaohuan Zhang, Xiulei Zhang, Yuan Zhang, Peiming Zheng, Jing Zhao and 1 more

Abstract read
In one paragraph

Article in Frontiers in cellular and infection microbiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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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

2 citing papers in PubMed.

  1. Article
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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.

Youhua Yuan *Department of Laboratory, Henan Provincial People's Hospital, Zhengzhou, Henan, China.
Yiman Geng *Department of Laboratory, Henan Provincial People's Hospital, Zhengzhou, Henan, China.
Tingjun Rong *Department of Laboratory, Xinyang Municipal Central Hospital, Xinyang, Henan, China.
Baoya WangDepartment of Laboratory, Henan Provincial People's Hospital, Zhengzhou, Henan, China.
Xiaohuan MaoDepartment of Laboratory, Henan Provincial People's Hospital, Zhengzhou, Henan, China.
Xiaohuan ZhangDepartment of Laboratory, Henan Provincial People's Hospital, Zhengzhou, Henan, China.
Xiulei ZhangDepartment of Laboratory, Henan Provincial People's Hospital, Zhengzhou, Henan, China.
Yuan ZhangDepartment of Laboratory, Henan Provincial People's Hospital, Zhengzhou, Henan, China.
Peiming ZhengDepartment of Laboratory, Henan Provincial People's Hospital, Zhengzhou, Henan, China.
Jing ZhaoDepartment of Laboratory, Henan Provincial People's Hospital, Zhengzhou, Henan, China.
Fengxia GuoDepartment of Laboratory, Henan Provincial People's Hospital, Zhengzhou, Henan, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: We established a reliable and cost-effective method for identifying severe acute respiratory syndrome coronavirus 2 variants circulating in central China and analysed the clinical characteristics of patients with acute coronavirus disease 2019 who were infected with these variants. Methods: The RNA of centrifuged and enriched samples was extracted and reverse transcribed into cDNA. cDNA was then analysed using a nested polymerase chain reaction amplification and Sanger sequencing method targeting specific mutations in the spike, Results: Among 172 isolates, JN.1.18.2 was the most prevalent (52.9%, 91/172), followed by XDV.1 (25.0%, 43/172), JN.1.16 (20.9%, 36/172), and KP.2 (1.2%, 2/172), which was found in central China for the first time. Fever with cough (52.6%, 80/152) was the most common symptom and 59.9% (91/152) of patients had underlying conditions. JN.1.18.2-infected patients more frequently presented with double-lung computed tomography changes. A strong positive correlation was observed between the duration from hospital admission to the detection of SARS-CoV-2 variants and total hospitalisation duration. Discussion: The new method provides a reliable tool for variant detection, highlighting milder clinical presentations in patients with active infections. Long-term monitoring of variants and patient characteristics is essential for effective prevention and treatment strategies.

Indexed as

COVID-19SARS-CoV-2AdolescentAdultAgedChinaCoronavirus Nucleocapsid ProteinsFemaleHigh-Throughput Nucleotide SequencingHumansMaleMiddle AgedMutationPolymerase Chain ReactionRNA, ViralSpike Glycoprotein, CoronavirusCoronavirus Nucleocapsid ProteinsRNA, ViralSpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2acute coronavirus disease 2019clinical characteristicnested PCRnext generation sequencingSARS-CoV-2 variant

Identifiers

PMID41262874
PMCPMC12623389

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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.