Evidence map›Paper›PMID 41288354›Full record

ArticleApplied and environmental microbiology2025

Genetic diversity and phylogenetic characteristics of human adenovirus strains 40/41 circulating in Yantai, China, during 2017-2019.

Peihua Niu, Pengcheng Du, Zhenlu Sun, Xiuhui Yao, Yiming Zhao, Ping Cheng, Qun Yang, Zetang Zhang, Xuejun Ma, Ji Wang

Abstract read
In one paragraph

Article in Applied and environmental microbiology, 2025. 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
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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

10 authors.

Peihua Niu *National Key Laboratory of Intelligent Tracking and Forecasting for Infectious Diseases, NHC Key Laboratory of Medical Virology and Viral Diseases, National Institute for Viral Disease Control and Prevention, Chinese Center for Disease Control and Prevention, Beijing, China.ORCID 0000-0001-5930-4234
Pengcheng Du *Medical Research Center, Beijing Institute of Respiratory Medicine and Beijing Chao-Yang Hospital, Capital Medical University, Beijing, China.
Zhenlu Sun *Yantai Center for Disease Control and Prevention, Yantai, Shandong, China.
Xiuhui YaoQitan Technology Ltd., Chengdu, China.
Yiming ZhaoNational Key Laboratory of Intelligent Tracking and Forecasting for Infectious Diseases, NHC Key Laboratory of Medical Virology and Viral Diseases, National Institute for Viral Disease Control and Prevention, Chinese Center for Disease Control and Prevention, Beijing, China.
Ping ChengNational Key Laboratory of Intelligent Tracking and Forecasting for Infectious Diseases, NHC Key Laboratory of Medical Virology and Viral Diseases, National Institute for Viral Disease Control and Prevention, Chinese Center for Disease Control and Prevention, Beijing, China.
Qun YangQitan Technology Ltd., Chengdu, China.
Zetang ZhangQitan Technology Ltd., Chengdu, China.
Xuejun MaNational Key Laboratory of Intelligent Tracking and Forecasting for Infectious Diseases, NHC Key Laboratory of Medical Virology and Viral Diseases, National Institute for Viral Disease Control and Prevention, Chinese Center for Disease Control and Prevention, Beijing, China.ORCID 0000-0002-9429-9036
Ji WangNational Key Laboratory of Intelligent Tracking and Forecasting for Infectious Diseases, NHC Key Laboratory of Medical Virology and Viral Diseases, National Institute for Viral Disease Control and Prevention, Chinese Center for Disease Control and Prevention, Beijing, China.ORCID 0009-0001-7457-298X

Funding

National Key Laboratory of Intelligent Tracking and Forecasting for Infectious Diseases ZDGWNLJS24-37National Key Research and Development Program of China No.2023YFC2306001
6 · The paper itself

Abstract

This study systematically characterizes the genetic diversity, phylogenetic relationships, recombination events, and structural variations of human adenovirus serotypes 40 and 41 (HAdV-F40/41) circulating in Shandong Province, China, between 2017 and 2019. A total of 2,221 stool samples were collected from patients presenting with acute gastroenteritis in Yantai. Enteric adenoviruses were identified using real-time quantitative PCR targeting the hexon gene. Whole-genome sequencing was performed via nanopore and Illumina platforms, enabling high-resolution phylogenetic reconstruction with IQ-TREE and the identification of recombination events using RDP5 and SimPlot. Evolutionary dynamics were inferred through Bayesian molecular clock analysis, while AlphaFold3-based structural modeling was used to assess the impact of genomic changes on the hexon protein. HAdV-F40/41 was detected in 94 samples (4.23%) with year-to-year variability in prevalence. Phylogenetic analysis revealed the co-circulation of multiple genetically distinct lineages, while recombination mapping identified key breakpoints, notably within the hexon and pVII genes. The estimated recent divergence of dominant lineages suggests ongoing adaptive evolution. Structural modeling of the recombinant strain SD376 identified 14 amino acid substitutions and three deletions relative to the reference strain OP378826.1, without substantial conformational alteration. These findings provide critical insights into the genomic plasticity and evolutionary potential of HAdV-F40/41, underscoring the importance of continuous genomic surveillance. The observed mutations and recombination patterns may facilitate immune escape and viral persistence, reinforcing the urgent need for improved monitoring strategies and the development of targeted vaccines. IMPORTANCE: Human adenovirus serotypes 40 and 41 (HAdV-F40/41) are among the leading viral causes of pediatric acute gastroenteritis worldwide, yet their genetic diversity and evolutionary dynamics remain poorly characterized in many regions, including China. In this study, we systematically investigated HAdV-F40/41 strains circulating in Yantai, Shandong Province, from 2017 to 2019. Using a combination of real-time PCR, nanopore sequencing, and next-generation sequencing, we elucidated the phylogenetic relationships, recombination events, and structural features of circulating strains. Our results reveal extensive genetic variability and the emergence of recombinant lineages with altered antigenic profiles, underscoring the role of adaptive evolution and potential immune escape. The identification of key mutations and recombination hotspots in hexon and pVII genes provides important molecular markers for surveillance and risk assessment. These findings enhance our understanding of HAdV-F40/41 evolution and highlight the urgent need for continuous genomic monitoring and targeted vaccine development to mitigate the public health burden of adenoviral gastroenteritis.

Indexed as

Adenoviruses, HumanAdenovirus Infections, HumanGenetic VariationPhylogenyChildChild, PreschoolChinaFecesFemaleGastroenteritisGenome, ViralHumansInfantMaleRecombination, GeneticAlphaFold3human adenovirusphylogeneticsrecombinationstructuralwhole-genome sequencing

Identifiers

PMID41288354
PMCPMC12724127

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.