Genetic and biological characterization of a reassortant H3N2 swine influenza virus isolated in China with internal genes from the 2009 pandemic H1N1.

Xuan Zhou1 Lili Sun1 Jingjing Yang1 Chenlu Xia2,3 Yuzhong Zhao4,5,6
Affiliations 6 institutions
  1. Jining Polytechnic, Jining, Shandong, 272007, China.
  2. College of Veterinary Medicine, Shandong Agricultural University, Tai'an, Shandong, 271018, China.
  3. Shandong Provincial Key Laboratory of Animal Biotechnology and Disease Control and Prevention, Shandong Agricultural University, Tai'an, Shandong, 271018, China.
  4. Jining Polytechnic, Jining, Shandong, 272007, China. [email protected].
  5. College of Veterinary Medicine, Shandong Agricultural University, Tai'an, Shandong, 271018, China. [email protected].
  6. Shandong Provincial Key Laboratory of Animal Biotechnology and Disease Control and Prevention, Shandong Agricultural University, Tai'an, Shandong, 271018, China. [email protected].

Abstract

Swine influenza virus (SIV) not only causes significant losses to the pig industry but also poses a potential threat to human health due to its ability for cross-species transmission and zoonotic characteristics. In this study, 600 nasal swab samples were collected from pigs in Shandong Province and tested for SIV using RT-qPCR. One sample tested positive, and the virus was successfully isolated in 10-day-old specific-pathogen-free (SPF) embryonated chicken eggs. Subtype-specific RT-PCR and sequencing identified the isolate as H3N2, designated A/swine/Shandong/116/2022 (H3N2). Whole-genome sequencing and similarity analysis showed that PB2, PB1, PA, NP, and M genes were most similar to H1N1 viruses (97.71-99.67%), while HA, NA, and NS genes were closest to H3N2 viruses (96.06-97.85%), suggesting this isolate is a reassortant between H1N1 and H3N2 viruses. Phylogenetic analysis indicated that PB2, PB1, PA, NP, and M genes belong to the 2009 pandemic H1N1 (pdm/09 H1N1) lineage, HA and NA genes belong to the human-like H3N2 (HL H3N2) lineage, and the NS gene belongs to the triple-reassortant (TR) H1N2 lineage. Key amino acid analysis showed a monobasic HA cleavage site (PEKQTR/G), consistent with low pathogenicity, and residues 190V, 226I, and 228S, which may affect receptor binding. PB2 residues 271A, 590S, and 591R may influence viral replication and host adaptation. Compared with the human influenza vaccine strain A/Darwin/9/2021 (H3N2), several amino acid changes were found in HA antigenic sites A, B, C, and E, suggesting possible antigenic drift. In addition, clear differences were found in N-linked glycosylation sites between the isolate and vaccine strain, including loss of several glycosylation sites and the appearance of a new site at position 499, which may change virus antigenicity and immune recognition. Functional studies demonstrated that the isolate efficiently infected MDCK cells and replicated in the respiratory tissues of BALB/c mice, causing mild to moderate lung lesions without mortality or significant weight loss. In summary, the isolated is a multi-source reassortant virus with low pathogenicity, providing valuable insights into the genetic characteristics and epidemiology of H3N2 SIV circulating in pigs in China.

Supporting text Virus Host Location
H3N2 7 Pathogenicity 54 Phylogenetic analysis 66 Reassortant virus 3 Swine influenza virus 6

Evidence records

10 total
Zoonotic Surveillance
2 records · 2 evidence types
Evidence type
1 records
OVE11792
Key finding

An H3N2 swine influenza virus, designated A/swine/Shandong/116/2022 (H3N2), was successfully isolated from a positive pig sample using 10-day-old SPF embryonated chicken eggs.

Virus
Host
Natural host
Location
Not specified
Supporting text

One sample tested positive, and the virus was successfully isolated in 10-day-old specific-pathogen-free (SPF) embryonated chicken eggs. ... identified the isolate as H3N2, designated A/swine/Shandong/116/2022 (H3N2).

Sample type
nasal swab
Evidence type
1 records
OVE11791
Key finding

RT-qPCR detected swine influenza virus in 1 of 600 pig nasal swabs collected in Shandong Province.

Virus
Host
Location
Supporting text

In this study, 600 nasal swab samples were collected from pigs in Shandong Province and tested for SIV using RT-qPCR. One sample tested positive

Method
RT-qPCR | Subtype-specific RT-PCR | sequencing
Sample type
nasal swab samples
Geographic raw
Shandong Province
Country inferred
CHN
Experimental Infection
3 records · 2 evidence types
Evidence type
1 records
OVE11800
Key finding

A/swine/Shandong/116/2022 (H3N2) caused mild to moderate lung lesions in BALB/c mice without mortality or significant weight loss while replicating in respiratory tissues.

Virus
Host
Location
Not specified
Supporting text

Subtype-specific RT-PCR and sequencing identified the isolate as H3N2, designated A/swine/Shandong/116/2022 (H3N2). Functional studies demonstrated that the isolate efficiently infected MDCK cells and replicated in the respiratory tissues of BALB/c mice, causing mild to moderate lung lesions without mortality or significant weight loss.

Method
in vivo infection of BALB/c mice | assessment of lung lesions (pathology/histopathology implied) | monitoring of mortality | monitoring of body weight | virus replication assessment in respiratory tissues
Experimental system
In vivo mouse infection model (BALB/c mice)
Evidence type
2 records
OVE11799
Key finding

A/swine/Shandong/116/2022 (H3N2) replicated in the respiratory tissues of BALB/c mice and caused mild to moderate lung lesions without mortality or significant weight loss.

Virus
Host
Location
Not specified
Supporting text

Functional studies demonstrated that the isolate efficiently infected MDCK cells and replicated in the respiratory tissues of BALB/c mice, causing mild to moderate lung lesions without mortality or significant weight loss.

Method
animal infection | tissue replication assessment | pathology/histopathology
Sample type
respiratory tissues | lung
Experimental system
animal challenge model (BALB/c mice)
Functional Mechanism
3 records · 1 evidence types
Evidence type
3 records
OVE11794
Key finding

In A/swine/Shandong/116/2022 (H3N2), HA residues 190V, 226I, and 228S are noted as potentially affecting receptor binding.

Virus
Host
Not specified
Location
Not specified
Supporting text

Subtype-specific RT-PCR and sequencing identified the isolate as H3N2, designated A/swine/Shandong/116/2022 (H3N2). Key amino acid analysis showed a monobasic HA cleavage site (PEKQTR/G), consistent with low pathogenicity, and residues 190V, 226I, and 228S, which may affect receptor binding.

Genes or proteins
HA
Mutations
190V | 226I | 228S
Mechanism types
receptor binding
OVE11795
Key finding

PB2 residues 271A, 590S, and 591R in A/swine/Shandong/116/2022 (H3N2) are associated with viral replication and host adaptation.

Virus
Host
Not specified
Location
Not specified
Supporting text

Subtype-specific RT-PCR and sequencing identified the isolate as H3N2, designated A/swine/Shandong/116/2022 (H3N2). PB2 residues 271A, 590S, and 591R may influence viral replication and host adaptation.

Genes or proteins
PB2
Mutations
271A | 590S | 591R
Mechanism types
replication adaptation | host-range expansion
OVE11796
Key finding

Relative to A/Darwin/9/2021 (H3N2), HA antigenic-site substitutions and altered N-linked glycosylation, including a new site at 499, in A/swine/Shandong/116/2022 (H3N2) suggest antigenic drift that may change immune recognition.

Virus
Host
Not specified
Location
Not specified
Supporting text

Compared with the human influenza vaccine strain A/Darwin/9/2021 (H3N2), several amino acid changes were found in HA antigenic sites A, B, C, and E, suggesting possible antigenic drift. In addition, clear differences were found in N-linked glycosylation sites between the isolate and vaccine strain, including loss of several glycosylation sites and the appearance of a new site at position 499, which may change virus antigenicity and immune recognition.

Genes or proteins
HA
Mutations
new N-linked glycosylation site at 499
Mechanism types
immune escape
Genomic Evolution
2 records · 2 evidence types
Evidence type
1 records
OVE11793
Key finding

An H3N2 swine influenza virus (A/swine/Shandong/116/2022) is a multi-source reassortant carrying internal genes from pdm/09 H1N1, HA/NA from human-like H3N2, and NS from triple‑reassortant H1N2.

Virus
Host
Not specified
Location
Not specified
Supporting text

PB2, PB1, PA, NP, and M genes were most similar to H1N1 viruses ... HA, NA, and NS genes were closest to H3N2 viruses ... suggesting this isolate is a reassortant between H1N1 and H3N2 viruses. Phylogenetic analysis indicated that PB2, PB1, PA, NP, and M genes belong to the 2009 pandemic H1N1 (pdm/09 H1N1) lineage, HA and NA genes belong to the human-like H3N2 (HL H3N2) lineage, and the NS gene belongs to the triple-reassortant (TR) H1N2 lineage.

Event type
reassortment
Genes or segments
PB2 | PB1 | PA | NP | M | HA | NA | NS
Evidence type
1 records
OVE11797
Key finding

Phylogenetic analysis of A/swine/Shandong/116/2022 (H3N2) shows internal genes PB2, PB1, PA, NP, and M from the 2009 pandemic H1N1 lineage, HA and NA from a human-like H3N2 lineage, and NS from a triple-reassortant H1N2 lineage.

Virus
Host
Location
Not specified
Supporting text

Subtype-specific RT-PCR and sequencing identified the isolate as H3N2, designated A/swine/Shandong/116/2022 (H3N2). Phylogenetic analysis indicated that PB2, PB1, PA, NP, and M genes belong to the 2009 pandemic H1N1 (pdm/09 H1N1) lineage, HA and NA genes belong to the human-like H3N2 (HL H3N2) lineage, and the NS gene belongs to the triple-reassortant (TR) H1N2 lineage.

Genes or proteins
PB2 | PB1 | PA | NP | M | HA | NA | NS
Analysis methods
phylogenetic analysis