Evidence map›Paper›PMID 38466094›Full record

ArticleJournal of virology2024

Recent H9N2 avian influenza virus lost hemagglutination activity due to a K141N substitution in hemagglutinin.

Feng Wen, Zhanfei Yan, Gaojie Chen, Yao Chen, Nina Wang, Zhili Li, Jinyue Guo, Hai Yu, Quan Liu, Shujian Huang

Open access · greenAbstract read
In one paragraph

Article in Journal of virology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

6 citing papers in PubMed, 7 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

10 authors at 2 institutions in 1 country.

Feng Wen *College of Life Science and Engineering, Foshan University, Foshan, Guangdong, China.ORCID 0000-0001-8790-1503
Zhanfei Yan *College of Life Science and Engineering, Foshan University, Foshan, Guangdong, China.
Gaojie ChenCollege of Life Science and Engineering, Foshan University, Foshan, Guangdong, China.
Yao ChenCollege of Life Science and Engineering, Foshan University, Foshan, Guangdong, China.
Nina WangCollege of Life Science and Engineering, Foshan University, Foshan, Guangdong, China.
Zhili LiCollege of Life Science and Engineering, Foshan University, Foshan, Guangdong, China.
Jinyue GuoCollege of Life Science and Engineering, Foshan University, Foshan, Guangdong, China.
Hai YuShanghai Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Shanghai, China.
Quan LiuCollege of Life Science and Engineering, Foshan University, Foshan, Guangdong, China.
Shujian HuangCollege of Life Science and Engineering, Foshan University, Foshan, Guangdong, China.ORCID 0000-0001-6561-5047
Foshan University · CNShanghai Veterinary Research Institute · CN

Funding

GDSTC | Basic and Applied Basic Research Foundation of Guangdong Province () 2022A1515012462MOST | National Natural Science Foundation of China (NSFC) 32002320
6 · The paper itself

Abstract

The H9N2 avian influenza virus (AIV) represents a significant risk to both the poultry industry and public health. Our surveillance efforts in China have revealed a growing trend of recent H9N2 AIV strains exhibiting a loss of hemagglutination activity at 37°C, posing challenges to detection and monitoring protocols. This study identified a single K141N substitution in the hemagglutinin (HA) glycoprotein as the culprit behind this diminished hemagglutination activity. The study evaluated the evolutionary dynamics of residue HA141 and studied the impact of the N141K substitution on aspects such as virus growth, thermostability, receptor-binding properties, and antigenic properties. Our findings indicate a polymorphism at residue 141, with the N variant becoming increasingly prevalent in recent Chinese H9N2 isolates. Although both wild-type and N141K mutant strains exclusively target α,2-6 sialic acid receptors, the N141K mutation notably impedes the virus's ability to bind to these receptors. Despite the mutation exerting minimal influence on viral titers, antigenicity, and pathogenicity in chicken embryos, it significantly enhances viral thermostability and reduces plaque size on Madin-Darby canine kidney (MDCK) cells. Additionally, the N141K mutation leads to decreased expression levels of HA protein in both MDCK cells and eggs. These findings highlight the critical role of the K141N substitution in altering the hemagglutination characteristics of recent H9N2 AIV strains under elevated temperatures. This emphasizes the need for ongoing surveillance and genetic analysis of circulating H9N2 AIV strains to develop effective control and prevention measures.IMPORTANCEThe H9N2 subtype of avian influenza virus (AIV) is currently the most prevalent low-pathogenicity AIV circulating in domestic poultry globally. Recently, there has been an emerging trend of H9N2 AIV strains acquiring increased affinity for human-type receptors and even losing their ability to bind to avian-type receptors, which raises concerns about their pandemic potential. In China, there has been a growing number of H9N2 AIV strains that have lost their ability to agglutinate chicken red blood cells, leading to false-negative results during surveillance efforts. In this study, we identified a K141N mutation in the HA protein of H9N2 AIV to be responsible for the loss of hemagglutination activity. This finding provides insight into the development of effective surveillance, prevention, and control strategies to mitigate the threat posed by H9N2 AIV to both animal and human health.

Indexed as

Amino Acid SubstitutionHemagglutinationHemagglutinin Glycoproteins, Influenza VirusInfluenza A Virus, H9N2 SubtypeInfluenza in BirdsMutationAnimalsCell LineChick EmbryoChickensDogsEvolution, MolecularFemaleHumansMicePoultryHemagglutinin Glycoproteins, Influenza VirusReceptors, Virusavian influenza virusH9N2haemagglutininhemagglutination activitymutationpoultrysurveillancethermostability

Identifiers

PMID38466094
PMCPMC11019909
OpenAlexW4392643963

What OpenQuestion holds

Textmetadata
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.