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

被引:1
作者
Wen, Feng [1 ,2 ]
Yan, Zhanfei [1 ]
Chen, Gaojie [1 ]
Chen, Yao [1 ]
Wang, Nina [1 ]
Li, Zhili [1 ]
Guo, Jinyue [1 ]
Yu, Hai [3 ]
Liu, Quan [1 ]
Huang, Shujian [1 ]
机构
[1] Foshan Univ, Coll Life Sci & Engn, Foshan, Guangdong, Peoples R China
[2] Foshan Univ, Coll Life Sci & Engn, Guangdong Prov Key Lab Anim Mol Design & Precise B, Foshan, Guangdong, Peoples R China
[3] Chinese Acad Agr Sci, Shanghai Vet Res Inst, Shanghai, Peoples R China
基金
中国国家自然科学基金;
关键词
avian influenza virus; hemagglutination activity; haemagglutinin; mutation; thermostability; surveillance; poultry; MOLECULAR CHARACTERIZATION; INTERNAL GENES; CHICKENS; CHINA; IDENTIFICATION; SPECIFICITY; POULTRY; LENGTH; ASSAY;
D O I
10.1128/jvi.00248-24
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
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 degrees 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 alpha,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. The 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.
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