College of Veterinary Medicine, Shandong Agricultural University, 61 Daizong Street, Tai'an, 271018, Shandong, China. [email protected].
Shandong Provincial Key Laboratory of Animal Biotechnology and Disease Control and Prevention, Shandong Agricultural University, Tai'an, 271018, Shandong, China. [email protected].
College of Veterinary Medicine, Shandong Agricultural University, 61 Daizong Street, Tai'an, 271018, Shandong, China.
Shandong Provincial Key Laboratory of Animal Biotechnology and Disease Control and Prevention, Shandong Agricultural University, Tai'an, 271018, Shandong, China.
College of Veterinary Medicine, Shandong Agricultural University, 61 Daizong Street, Tai'an, 271018, Shandong, China. [email protected].
Shandong Provincial Key Laboratory of Animal Biotechnology and Disease Control and Prevention, Shandong Agricultural University, Tai'an, 271018, Shandong, China. [email protected].
College of Veterinary Medicine, Shandong Agricultural University, 61 Daizong Street, Tai'an, 271018, Shandong, China. [email protected].
Shandong Provincial Key Laboratory of Animal Biotechnology and Disease Control and Prevention, Shandong Agricultural University, Tai'an, 271018, Shandong, China. [email protected].
H9N2 avian influenza virus (AIV) has been circulating in poultry in China for decades and are undergoing adaptation to mammals, posing potential pandemic risks. To investigate the prevalence of H9N2 AIVs in swine, we conducted surveillance in Shandong Province from 2021 to 2023. Two H9N2 influenza virus strains, A/swine/Shandong/417/2021(Sw/SD/417/21) and A/swine/Shandong/662/2022 (Sw/SD/662/22), were successfully isolated from swine and genetically characterized. Phylogenetic analyses showed that both isolates were reassortants containing gene segments from multiple H9N2 AIV lineages and closely related to currently circulating H9N2 AIV. Key molecular marker analysis revealed that both isolates carried mammalian-adaptive residues in the HA receptor-binding sites (183 N, 190 V, 226 L), a novel HA cleavage site variant (PSKSSRGL), PB2 mutations (A588V, E627V), and the M2 S31N substitution, suggesting potential adaptation to mammalian hosts and resistance to adamantane antivirals. Mice infection experiments demonstrated efficient viral replication in the respiratory tract, particularly in the lungs, but only mild histopathological changes were observed, with no significant weight loss or mortality, indicating low pathogenicity in mice. Serological surveillance of 3,172 swine serum samples showed a low prevalence of H9N2 influenza virus infection (0.44%), with positive samples sporadically distributed across regions and years. In summary, although H9N2 AIV infection in swine is rare and generally mild, the presence of mammalian-adaptive markers and reassortant genomes highlights the potential risk of cross-species transmission and subclinical adaptation. Continuous avian-swine-human influenza surveillance is therefore essential to mitigate the potential threat posed by H9N2 AIV.
Two H9N2 influenza virus strains, A/swine/Shandong/417/2021 and A/swine/Shandong/662/2022, were successfully isolated from swine and genetically characterized.
Mice infection experiments demonstrated efficient viral replication in the respiratory tract, particularly in the lungs, but only mild histopathological changes were observed, with no significant weight loss or mortality.
Method
infection experiment
Study design
animal experiment
Transmission direction
host-range experiment
Event type
mouse infection model
Molecular Adaptation1 records
Molecular AdaptationExtraction confidence 0.95
Key finding
H9N2 swine isolates carried mammalian-adaptive residues in HA and PB2 and an antiviral resistance mutation in M2, suggesting adaptation to mammalian hosts.
Key molecular marker analysis revealed that both isolates carried mammalian-adaptive residues in the HA receptor-binding sites (183 N, 190 V, 226 L), a novel HA cleavage site variant (PSKSSRGL), PB2 mutations (A588V, E627V), and the M2 S31N substitution, suggesting potential adaptation to mammalian hosts and resistance to adamantane antivirals.
Method
molecular marker analysis
Study design
comparative genomics
Transmission direction
molecular mechanism only
Event type
mammalian-adaptive mutations
Geographic raw
China
Country inferred
CHN
Genes or proteins
HA | PB2 | M2
Mutations
HA 183N | HA 190V | HA 226L | HA cleavage site PSKSSRGL | PB2 A588V | PB2 E627V | M2 S31N
Mechanism types
mammalian adaptation | antiviral resistance
Recombination Or Reassortment1 records
Recombination Or ReassortmentExtraction confidence 0.90
Key finding
The H9N2 swine isolates were reassortants containing gene segments from multiple H9N2 lineages.
Phylogenetic analyses showed that both isolates were reassortants containing gene segments from multiple H9N2 AIV lineages and closely related to currently circulating H9N2 AIV.
Method
genome sequencing | phylogenetic comparison
Study design
phylogenetic analysis
Transmission direction
molecular mechanism only
Event type
reassortant genome structure
Geographic raw
China
Country inferred
CHN
Genes or proteins
multiple gene segments
Mechanism types
reassortment
Zoonotic Surveillance1 records
Zoonotic SurveillanceExtraction confidence 0.88
Key finding
Serological testing of 3,172 swine samples detected 0.44% H9N2 antibody prevalence, indicating low-level exposure in pigs.
Serological surveillance of 3,172 swine serum samples showed a low prevalence of H9N2 influenza virus infection (0.44%), with positive samples sporadically distributed across regions and years.