Evidence map›Paper›PMID 41327480›Full record

ArticleVeterinary research2025

Adaptive mutations in HA of avian H9N2 influenza viruses facilitate their transmission to swine.

Jia Wang, Peiwen Chen, Qiwei Liu, Sixia Huang, Maocai Wu, Dan'er Wei, Wenshan Hong, Tommy Tsan-Yuk Lam, Huachen Zhu, Yi Guan

Abstract read
In one paragraph

Article in Veterinary research, 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.

Jia WangGuangdong-Hong Kong Joint Laboratory of Emerging Infectious Diseases/Joint Laboratory for International Collaboration in Virology and Emerging Infectious Diseases, Joint Institute of Virology (STU/HKU), Shantou University, Daxue Road 243, Jinping District, Shantou, Guangdong, People's Republic of China. jwang123@stu.edu.cn.
Peiwen ChenGuangdong-Hong Kong Joint Laboratory of Emerging Infectious Diseases/Joint Laboratory for International Collaboration in Virology and Emerging Infectious Diseases, Joint Institute of Virology (STU/HKU), Shantou University, Daxue Road 243, Jinping District, Shantou, Guangdong, People's Republic of China.
Qiwei LiuGuangdong-Hong Kong Joint Laboratory of Emerging Infectious Diseases/Joint Laboratory for International Collaboration in Virology and Emerging Infectious Diseases, Joint Institute of Virology (STU/HKU), Shantou University, Daxue Road 243, Jinping District, Shantou, Guangdong, People's Republic of China.
Sixia HuangGuangdong-Hong Kong Joint Laboratory of Emerging Infectious Diseases/Joint Laboratory for International Collaboration in Virology and Emerging Infectious Diseases, Joint Institute of Virology (STU/HKU), Shantou University, Daxue Road 243, Jinping District, Shantou, Guangdong, People's Republic of China.
Maocai WuGuangdong-Hong Kong Joint Laboratory of Emerging Infectious Diseases/Joint Laboratory for International Collaboration in Virology and Emerging Infectious Diseases, Joint Institute of Virology (STU/HKU), Shantou University, Daxue Road 243, Jinping District, Shantou, Guangdong, People's Republic of China.
Dan'er WeiGuangdong-Hong Kong Joint Laboratory of Emerging Infectious Diseases/Joint Laboratory for International Collaboration in Virology and Emerging Infectious Diseases, Joint Institute of Virology (STU/HKU), Shantou University, Daxue Road 243, Jinping District, Shantou, Guangdong, People's Republic of China.
Wenshan HongGuangdong-Hong Kong Joint Laboratory of Emerging Infectious Diseases/Joint Laboratory for International Collaboration in Virology and Emerging Infectious Diseases, Joint Institute of Virology (STU/HKU), Shantou University, Daxue Road 243, Jinping District, Shantou, Guangdong, People's Republic of China.
Tommy Tsan-Yuk LamGuangdong-Hong Kong Joint Laboratory of Emerging Infectious Diseases/Joint Laboratory for International Collaboration in Virology and Emerging Infectious Diseases, Joint Institute of Virology (STU/HKU), Shantou University, Daxue Road 243, Jinping District, Shantou, Guangdong, People's Republic of China.
Huachen ZhuGuangdong-Hong Kong Joint Laboratory of Emerging Infectious Diseases/Joint Laboratory for International Collaboration in Virology and Emerging Infectious Diseases, Joint Institute of Virology (STU/HKU), Shantou University, Daxue Road 243, Jinping District, Shantou, Guangdong, People's Republic of China.
Yi GuanGuangdong-Hong Kong Joint Laboratory of Emerging Infectious Diseases/Joint Laboratory for International Collaboration in Virology and Emerging Infectious Diseases, Joint Institute of Virology (STU/HKU), Shantou University, Daxue Road 243, Jinping District, Shantou, Guangdong, People's Republic of China. yguan@hku.hk.

Funding

Excellent Young Scientists Fund, National Natural Science Foundation of China 31922087Guangdong Provincial Department of Science and Technology 2015A020213008,190824215544727, 2019B121205009, 190830095586328, and 200109155890863,National Natural Science Foundation of China 31200948Shenzhen-Hong Kong Science and Technology Cooperation Zone-Shenzhen Programme HZQB-KCZYZ-2021014
6 · The paper itself

Abstract

The cross-species transmission of avian H9N2 influenza viruses to swine increases the risk of viral adaptation to mammalian hosts. However, the mechanisms by which these H9 viruses can overcome the barriers posed by swine hosts have not yet been fully elucidated. In previous studies, we identified avian H9 strains exhibiting either infective or noninfective phenotypes in swine. Here, we investigated the role of surface genes in cross-species transmission by replacing the surface genes of noninfective strains with those of their infective counterparts. We demonstrated that the surface genes of the infective strains, particularly the hemagglutinin (HA) gene, restored infectivity in pigs for two previously noninfective strains. Surface genes from infective strains significantly increased viral replication efficiency in both CEF and PK15 cells, and recombinant viruses carrying these genes presented superior thermal stability. Amino acid sequence analysis of HA identified six critical residues (30T, 39A, 327R, 373K, 465K, and 490R) associated with infectivity in pigs. Avian H9 viruses bearing these swine-adaptive molecular signatures began emerging in terrestrial poultry before the 2000s and subsequently achieved dominance through widespread dissemination. These findings suggest that molecular changes in HA accumulated during the adaptation of avian H9 viruses in terrestrial poultry may drive the emergence of swine-infective strains. This study elucidates key molecular determinants that enable avian H9 viruses to infect swine and highlights the public health implications of prolonged H9N2 circulation in terrestrial poultry, which facilitates mammalian adaptation. These insights underscore the need for intensified surveillance of avian-to-swine influenza transmission dynamics.

Indexed as

Hemagglutinin Glycoproteins, Influenza VirusInfluenza A Virus, H9N2 SubtypeInfluenza in BirdsOrthomyxoviridae InfectionsSwine DiseasesAnimalsMutationSwineHemagglutinin Glycoproteins, Influenza Viruscross-species transmissionH9N2 avian influenza virushemagglutinin (HA) mutationsswine infectivityviral adaptation

Identifiers

PMID41327480
PMCPMC12777327

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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.