Evidence map›Paper›PMID 37585307›Full record

ArticleEmerging microbes & infections2023

Emergence of a new designated clade 16 with significant antigenic drift in hemagglutinin gene of H9N2 subtype avian influenza virus in eastern China.

Xiyue Wang, Kaituo Liu, Yaqian Guo, Yuru Pei, Xia Chen, Xiaolong Lu, Ruyi Gao, Yu Chen, Min Gu, Jiao Hu and 5 more

Open access · goldAbstract read
In one paragraph

Article in Emerging microbes & infections, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.4field-weighted citation impact, top 11% of its field
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

11 citing papers in PubMed, 11 citations in OpenAlex.

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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

15 authors at 1 institution in 1 country.

Xiyue WangCollege of Veterinary Medicine, Yangzhou University, Yangzhou, People's Republic of China.
Kaituo LiuCollege of Veterinary Medicine, Yangzhou University, Yangzhou, People's Republic of China.
Yaqian GuoCollege of Veterinary Medicine, Yangzhou University, Yangzhou, People's Republic of China.
Yuru PeiCollege of Veterinary Medicine, Yangzhou University, Yangzhou, People's Republic of China.
Xia ChenCollege of Veterinary Medicine, Yangzhou University, Yangzhou, People's Republic of China.
Xiaolong LuCollege of Veterinary Medicine, Yangzhou University, Yangzhou, People's Republic of China.
Ruyi GaoCollege of Veterinary Medicine, Yangzhou University, Yangzhou, People's Republic of China.
Yu ChenCollege of Veterinary Medicine, Yangzhou University, Yangzhou, People's Republic of China.
Min GuCollege of Veterinary Medicine, Yangzhou University, Yangzhou, People's Republic of China.
Jiao HuCollege of Veterinary Medicine, Yangzhou University, Yangzhou, People's Republic of China.
Xiaowen LiuCollege of Veterinary Medicine, Yangzhou University, Yangzhou, People's Republic of China.
Shunlin HuCollege of Veterinary Medicine, Yangzhou University, Yangzhou, People's Republic of China.
Xin-An JiaoJoint International Research Laboratory of Agriculture and Agri-Product Safety, The Ministry of Education of China, Yangzhou University, Yangzhou, People's Republic of China.
Xiufan LiuCollege of Veterinary Medicine, Yangzhou University, Yangzhou, People's Republic of China.
Xiaoquan WangCollege of Veterinary Medicine, Yangzhou University, Yangzhou, People's Republic of China.
Yangzhou University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

H9N2 avian influenza viruses (AIVs) pose an increasing threat to the poultry industry worldwide and have pandemic potential. Vaccination has been principal prevention strategy to control H9N2 in China since 1998, but vaccine effectiveness is persistently challenged by the emergence of the genetic and/or antigenic variants. Here, we analysed the genetic and antigenic characteristics of H9N2 viruses in China, including 70 HA sequences of H9N2 isolates from poultry, 7358 from online databases during 2010-2020, and 15 from the early reference strains. Bayesian analyses based on hemagglutinin (HA) gene revealed that a new designated clade16 emerged in April 2012, and was prevalent and co-circulated with clade 15 since 2013 in China. Clade 16 viruses exhibited decreased cross-reactivity with those from clade 15. Antigenic Cartography analyses showed represent strains were classified into three antigenic groups named as Group1, Group2 and Group3, and most of the strains in Group 3 (15/17, 88.2%) were from Clade 16 while most of the strains in Group2 (26/29, 89.7%) were from Clade 15. The mean distance between Group 3 and Group 2 was 4.079 (95%CI 3.605-4.554), revealing that major switches to antigenic properties were observed over the emergence of clade 16. Genetic analysis indicated that 11 coevolving amino acid substitutions primarily at antigenic sites were associated with the antigenic differences between clade 15 and clade 16. These data highlight complexities of the genetic evolution and provide a framework for the genetic basis and antigenic characterization of emerging clade 16 of H9N2 subtype avian influenza virus.

Indexed as

Influenza A Virus, H9N2 SubtypeInfluenza in BirdsAnimalsAntigenic Drift and ShiftBayes TheoremChickensChinaHemagglutinin Glycoproteins, Influenza VirusHemagglutininsPhylogenyPoultryHemagglutinin Glycoproteins, Influenza VirusHemagglutininsantigenicgenetic evolutionH9N2HA genenew designated clade

Identifiers

PMID37585307
PMCPMC10467529
OpenAlexW4385872119

What OpenQuestion holds

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LicenceCC BY
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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.