Genetic evolution and molecular characteristics of avian influenza viruses in Jining from 2018 to 2023.

Mingsheng Zhao1 Huixin Dou2 Yajuan Jiang2 Yongjian Jia2 Ying Yue3 Libo Li3 Shiqing Huang3 Meidi Si1 Jingjing Wang1 Boyan Jiao2 Xiaoyu Wang2
Affiliations 3 institutions
  1. Institute of Immunology and Molecular Medicine, Jining Medical University, Jining, China.
  2. Department of Microbiological Laboratory, Jining Center for Disease Control and Prevention, Jining, China.
  3. Department of Infectious Disease Control, Jining Center for Disease Control and Prevention, Jining, China.

Abstract

This study aimed to analyze the genetic evolution and molecular characteristics of H5, H7, and H9 subtypes of avian influenza viruses in the external environment of poultry in Jining from 2018 to 2023, providing scientific evidence for the prevention and control of avian influenza. Positive samples of H5, H7, and H9 subtypes, collected from the poultry external environment in Jining between 2018 and 2023, were subjected to real-time quantitative PCR. Samples with cycle threshold (CT) values below 30 were selected for influenza virus capture and whole-genome sequencing. Phylogenetic analysis was conducted using bioinformatics software to construct an evolutionary tree, and amino acid mutation sites in the avian influenza virus sequences were analyzed. Whole-genome sequencing was completed for seven H5N1 strains, four H5N6 strains, one H7N9 strain, and 30 H9N2 strains. Homology analysis revealed that the nucleotide and amino acid sequences of the H5N1 subtype exhibited lower homology with those of the H5N6, H7N9, and H9N2 subtypes, indicating a greater genetic distance. Phylogenetic and molecular characteristic analyses showed that the seven H5N1 strains, four H5N6 strains, and one H7N9 strain were highly pathogenic, while all 30 H9N2 strains were low pathogenic. No mutations were identified at most receptor-binding sites, such as Q226L and G228S, in the H5N1, H5N6, and H7N9 strains, indicating limited mutation at these sites. However, some mutations were observed, suggesting that the virus retained some binding affinity for the human receptor α-2,6Gal. In contrast, mutations at receptor-binding sites, including G186V, A190T, and Q226L, were found in most of the H9N2 strains, increasing their likelihood of binding to α-2,6Gal and indicating a higher potential for human infection. The H5, H7, and H9 subtypes of avian influenza viruses are undergoing continuous dynamic evolution and exhibit significant genetic diversity. Enhanced monitoring of viral molecular evolution and research into cross-host transmission are essential.

Supporting text Virus Host Location
avian influenza virus 59 genetic evolution 12 H5N1 82 H5N6 6 H7N9 27 H9N2 27 molecular characteristics 2

Evidence records

3 total
Zoonotic Surveillance
3 records · 1 evidence types
Evidence type
3 records
OVE9038
Key finding

H5 avian influenza virus subtype was detected in poultry external environment samples in Jining between 2018 and 2023 using real-time quantitative PCR.

Virus
Host
Location
Supporting text

Positive samples of H5 subtype, collected from the poultry external environment in Jining between 2018 and 2023, were subjected to real-time quantitative PCR.

Method
real-time quantitative PCR
Sample type
external environment samples
Geographic raw
Jining
Country inferred
CHN
OVE9039
Key finding

H7 avian influenza virus subtype was detected in poultry external environment samples in Jining between 2018 and 2023 using real-time quantitative PCR.

Virus
Host
Location
Supporting text

Positive samples of H7 subtype, collected from the poultry external environment in Jining between 2018 and 2023, were subjected to real-time quantitative PCR.

Method
real-time quantitative PCR
Sample type
external environment samples
Geographic raw
Jining
Country inferred
CHN
OVE9040
Key finding

H9 avian influenza virus subtype was detected in poultry external environment samples in Jining between 2018 and 2023 using real-time quantitative PCR.

Virus
Host
Location
Supporting text

Positive samples of H9 subtype, collected from the poultry external environment in Jining between 2018 and 2023, were subjected to real-time quantitative PCR.

Method
real-time quantitative PCR
Sample type
external environment samples
Geographic raw
Jining
Country inferred
CHN