The HA and NS genes of human H5N1 influenza A virus contribute to high virulence in ferrets.

Hirotaka Imai1 Kyoko Shinya Ryo Takano Maki Kiso Yukiko Muramoto Saori Sakabe Shin Murakami Mutsumi Ito Shinya Yamada Mai Thi Quynh Le Chairul A Nidom Yuko Sakai-Tagawa Kei Takahashi Yasuyuki Omori Takeshi Noda Masayuki Shimojima Satoshi Kakugawa Hideo Goto Kiyoko Iwatsuki-Horimoto Taisuke Horimoto Yoshihiro Kawaoka
Affiliations 1 institutions
  1. Division of Virology, Department of Microbiology and Immunology, Institute of Medical Science, The University of Tokyo, Tokyo, Japan.

Abstract

Highly pathogenic H5N1 influenza A viruses have spread across Asia, Europe, and Africa. More than 500 cases of H5N1 virus infection in humans, with a high lethality rate, have been reported. To understand the molecular basis for the high virulence of H5N1 viruses in mammals, we tested the virulence in ferrets of several H5N1 viruses isolated from humans and found A/Vietnam/UT3062/04 (UT3062) to be the most virulent and A/Vietnam/UT3028/03 (UT3028) to be avirulent in this animal model. We then generated a series of reassortant viruses between the two viruses and assessed their virulence in ferrets. All of the viruses that possessed both the UT3062 hemagglutinin (HA) and nonstructural protein (NS) genes were highly virulent. By contrast, all those possessing the UT3028 HA or NS genes were attenuated in ferrets. These results demonstrate that the HA and NS genes are responsible for the difference in virulence in ferrets between the two viruses. Amino acid differences were identified at position 134 of HA, at positions 200 and 205 of NS1, and at positions 47 and 51 of NS2. We found that the residue at position 134 of HA alters the receptor-binding property of the virus, as measured by viral elution from erythrocytes. Further, both of the residues at positions 200 and 205 of NS1 contributed to enhanced type I interferon (IFN) antagonistic activity. These findings further our understanding of the determinants of pathogenicity of H5N1 viruses in mammals.

Supporting text Virus Host Location
Animals 1948 Cells, Cultured 26 Dogs 176 Ferrets 79 Hemagglutinin Glycoproteins, Influenza Virus 180 Humans 1440 Influenza A Virus, H5N1 Subtype 300 Influenza, Human 286 Interferons 10 Kidney 8 Lung 65 Male 224 Mink 48 Mutation 209 Orthomyxoviridae Infections 228 Viral Nonstructural Proteins 28 Virulence 108 INS1 protein, influenza virus 7

Evidence records

3 total
Experimental Infection
2 records · 1 evidence types
Evidence type
2 records
OVE861
Key finding

A/Vietnam/UT3062/04 was highly virulent while A/Vietnam/UT3028/03 was avirulent in experimentally infected ferrets.

Virus
Host
Location
Not specified
Supporting text

We tested the virulence in ferrets of several H5N1 viruses isolated from humans and found A/Vietnam/UT3062/04 (UT3062) to be the most virulent and A/Vietnam/UT3028/03 (UT3028) to be avirulent in this animal model.

Method
experimental infection | clinical observation of disease phenotype | assessment of virulence
Experimental system
ferret infection model
OVE862
Key finding

Reassortant H5N1 viruses carrying HA and NS genes from A/Vietnam/UT3062/04 were highly virulent in ferrets, whereas those carrying HA or NS from A/Vietnam/UT3028/03 were attenuated.

Virus
Host
Location
Not specified
Supporting text

We then generated a series of reassortant viruses between the two viruses and assessed their virulence in ferrets. All of the viruses that possessed both the UT3062 hemagglutinin (HA) and nonstructural protein (NS) genes were highly virulent. By contrast, all those possessing the UT3028 HA or NS genes were attenuated in ferrets.

Method
generation of reassortant viruses | experimental infection of ferrets | assessment of virulence based on disease severity and mortality
Experimental system
ferret infection model with reassortant H5N1 viruses
Functional Mechanism
1 records · 1 evidence types
Evidence type
1 records
OVE864
Key finding

Residues 200 and 205 of the NS1 protein in H5N1 influenza A virus enhance type I interferon antagonistic activity, contributing to increased virulence.

Virus
Host
Not specified
Location
Not specified
Supporting text

Both of the residues at positions 200 and 205 of NS1 contributed to enhanced type I interferon (IFN) antagonistic activity.

Genes or proteins
NS1
Host factors
type I interferon
Mutations
residue 200 | residue 205
Mechanism types
immune escape | virulence adaptation