The emergence of novel H3N8 and H3N3 avian influenza viruses in chickens during multi-province surveillance in China and their potential public health risk.

Xue Wang1,2 Hao Shi2 Peidong Li2 Hao Zhu2 Naijia Zhang2 Qingqing Song2 Shouchuan Liu3 Qingquan Lu4 Abdul Khalique5 Muhammad Kashif Saleemi6 Zhaoyang Li5 Chunguo Liu7 Limin Li8
Affiliations 8 institutions
  1. College of Veterinary Medicine, Hebei Agricultural University, Baoding 071000, Hebei, China
  2. Group Biological Products R & D Center, Shandong Sinder Technology Co., Ltd., Qingdao 266100, Shandong, China.
  3. Shandong Hile Biological Products Co., Ltd., Weifang 262233, Shandong, China.
  4. Shandong Feed and Veterinary Drug Quality Inspection Center, Jinan 250110, Shandong, China.
  5. Shandong Sinder Technology Co., Ltd., Qingdao 266100, Shandong, China.
  6. Department of Pathology, University of Agriculture Faisalabad, Faisalabad 38040, Punjab, Pakistan.
  7. Group Biological Products R & D Center, Shandong Sinder Technology Co., Ltd., Qingdao 266100, Shandong, China. Electronic address: [email protected].
  8. College of Veterinary Medicine, Hebei Agricultural University, Baoding 071000, Hebei, China. Electronic address: [email protected].

Abstract

The H3 subtype avian influenza virus (AIV) poses a substantial global public health threat due to its high host adaptability and ongoing evolution. The recent emergence of novel H3N8 and H3N3 AIVs associated with cross-species transmission underscores the urgent need for enhanced epidemiological surveillance. In this study, we conducted surveillance and characterization of H3 AIVs based on a total of 737 poultry samples collected across 21 Chinese provinces from November 2022 to December 2023. Of these, 69 (9.4%) tested positive for H3 AIV by RT-qPCR, and one H3N8 isolate and ten H3N3 isolates were obtained for whole-genome characterization. We performed whole-genome sequencing, phylogenetic analysis, reassortment inference, and evaluation of key amino acid substitutions, alongside antigenic characterization using hemagglutination inhibition (HI) assays and an in vivo mouse challenge experiment. The H3N8 isolate was identified as a triple-reassortant virus possessing the Eurasian avian H3 gene, the North American avian N8 gene, and H9N2-derived internal genes. The H3N3 isolates represented reassortant viruses that had acquired the HA gene from the novel H3N8 AIV lineage, the NA gene from H10N3 AIV, and internal genes from H9N2 AIV. All isolates exhibited HA cleavage sites characteristic of low pathogenic avian influenza viruses. Additionally, several amino acid substitutions previously associated with enhanced mammalian adaptation were identified, including L89V and I292V in PB2 and H436Y in PB1. In a BALB/c mouse challenge experiment, the representative H3N8 virus established infection without prior adaptation and replicated predominantly in the upper respiratory tract, with detectable viral RNA in respiratory tissues and limited extrapulmonary dissemination. Antigenic analysis revealed no cross-reactivity between the novel H3 AIVs and H5, H7, or H9 AIVs as measured by HI. Based on molecular and phylogenetic characterization, antigenic assessment, and preliminary mammalian infection data, our findings provide evidence suggesting a potential public health risk. We recommend intensified surveillance of H3 AIVs in poultry and accelerated vaccine development to curb viral spread and improve public health preparedness.

Supporting text Virus Host Location
Genetic reassortment 4 H3 AIVs 1 Mammalian adaptation 4 Phylogenetic analysis 66 Virus isolation 7 Whole-genome sequencing 9

Evidence records

9 total
Zoonotic Surveillance
3 records · 3 evidence types
Evidence type
1 records
OVE11622
Key finding

One H3N8 and ten H3N3 avian influenza viruses were isolated from poultry samples in China.

Virus
Host
Location
Not specified
Supporting text

In this study, we conducted surveillance and characterization of H3 AIVs based on a total of 737 poultry samples collected across 21 Chinese provinces from November 2022 to December 2023. Of these, 69 (9.4%) tested positive for H3 AIV by RT-qPCR, and one H3N8 isolate and ten H3N3 isolates were obtained for whole-genome characterization.

Sample type
poultry samples
Evidence type
1 records
OVE11621
Key finding

H3 avian influenza virus was detected in poultry surveillance samples in China, with 69 of 737 (9.4%) testing positive by RT-qPCR across 21 Chinese provinces.

Virus
Host
Location
Supporting text

In this study, we conducted surveillance and characterization of H3 AIVs based on a total of 737 poultry samples collected across 21 Chinese provinces from November 2022 to December 2023. Of these, 69 (9.4%) tested positive for H3 AIV by RT-qPCR

Method
RT-qPCR
Sample type
poultry samples
Geographic raw
China | 21 Chinese provinces
Country inferred
CHN
Evidence type
1 records
OVE11627
Key finding

HI assays showed no cross-reactivity between the novel H3 avian influenza viruses and H5, H7, or H9 avian influenza viruses.

Virus
Host
Location
Not specified
Supporting text

Antigenic analysis revealed no cross-reactivity between the novel H3 AIVs and H5, H7, or H9 AIVs as measured by HI.

Method
hemagglutination inhibition (HI) assay
Sample type
serum (HI assay)
Experimental Infection
1 records · 1 evidence types
Evidence type
1 records
OVE11626
Key finding

A representative H3N8 avian influenza virus infected BALB/c mice without prior adaptation, replicating mainly in the upper respiratory tract with limited extrapulmonary dissemination.

Virus
Host
Location
Not specified
Supporting text

In a BALB/c mouse challenge experiment, the representative H3N8 virus established infection without prior adaptation and replicated predominantly in the upper respiratory tract, with detectable viral RNA in respiratory tissues and limited extrapulmonary dissemination.

Method
in vivo mouse challenge | viral RNA detection (e.g., RT-qPCR) in tissues
Experimental system
BALB/c mouse challenge experiment (in vivo animal model)
Functional Mechanism
1 records · 1 evidence types
Evidence type
1 records
OVE11625
Key finding

H3 avian influenza isolates harbored PB2 L89V, PB2 I292V, and PB1 H436Y substitutions previously linked to enhanced mammalian adaptation.

Virus
Host
Not specified
Location
Not specified
Supporting text

several amino acid substitutions previously associated with enhanced mammalian adaptation were identified, including L89V and I292V in PB2 and H436Y in PB1.

Genes or proteins
PB2 | PB1
Mutations
PB2 L89V | PB2 I292V | PB1 H436Y
Mechanism types
host-range expansion | replication adaptation
Genomic Evolution
4 records · 2 evidence types
Evidence type
2 records
OVE11623
Key finding

An H3N8 isolate was a triple-reassortant with Eurasian avian H3, North American avian N8, and H9N2-derived internal genes.

Virus
Host
Not specified
Location
Not specified
Supporting text

The H3N8 isolate was identified as a triple-reassortant virus possessing the Eurasian avian H3 gene, the North American avian N8 gene, and H9N2-derived internal genes.

Event type
reassortment
Genes or segments
HA (H3) | NA (N8) | internal genes
OVE11624
Key finding

H3N3 isolates were reassortants with HA from the novel H3N8 AIV lineage, NA from H10N3 AIV, and internal genes from H9N2 AIV.

Virus
Host
Not specified
Location
Not specified
Supporting text

The H3N3 isolates represented reassortant viruses that had acquired the HA gene from the novel H3N8 AIV lineage, the NA gene from H10N3 AIV, and internal genes from H9N2 AIV.

Event type
reassortment
Genes or segments
HA | NA | internal genes
Evidence type
2 records
OVE11628
Key finding

Phylogenetic whole‑genome analysis showed the H3N8 isolate is a triple‑reassortant with a Eurasian avian H3 gene, a North American avian N8 gene, and H9N2‑derived internal genes.

Virus
Host
Not specified
Location
Not specified
Supporting text

We performed whole-genome sequencing, phylogenetic analysis, reassortment inference, and evaluation of key amino acid substitutions. The H3N8 isolate was identified as a triple-reassortant virus possessing the Eurasian avian H3 gene, the North American avian N8 gene, and H9N2-derived internal genes.

Genes or proteins
H3 gene | N8 gene | internal genes
Analysis methods
whole-genome sequencing | phylogenetic analysis | reassortment inference
OVE11629
Key finding

Phylogenetic analysis indicated the H3N3 isolates are reassortants with HA derived from the novel H3N8 lineage, NA from H10N3, and internal genes from H9N2.

Virus
Host
Not specified
Location
Not specified
Supporting text

We performed whole-genome sequencing, phylogenetic analysis, reassortment inference, and evaluation of key amino acid substitutions. The H3N3 isolates represented reassortant viruses that had acquired the HA gene from the novel H3N8 AIV lineage, the NA gene from H10N3 AIV, and internal genes from H9N2 AIV.

Genes or proteins
HA gene | NA gene | internal genes
Analysis methods
whole-genome sequencing | phylogenetic analysis | reassortment inference