Literature detail

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.
PMID 20862325 2010 PLoS Pathog eng epublish
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Article

Publication summary

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.

Animals Cells, Cultured Dogs Ferrets Hemagglutinin Glycoproteins, Influenza Virus Humans Influenza A Virus, H5N1 Subtype Influenza, Human Interferons Kidney Lung Male Mink Mutation Orthomyxoviridae Infections Viral Nonstructural Proteins Virulence INS1 protein, influenza virus

Structured evidence records

Evidence records

5 total
2 records
Extraction confidence 0.95
Key finding

Amino acid residue 134 in the HA of H5N1 influences receptor-binding properties, contributing to virulence differences in ferrets.

Virus
Host
Not specified
Location
Not specified
Supporting text

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.

Genes or proteins
HA
Receptors
receptor-binding property
Mutations
HA position 134
Mechanism types
receptor_binding; pathogenicity
Extraction confidence 0.95
Key finding

NS1 residues 200 and 205 in H5N1 enhance type I interferon antagonism, associated with increased virulence in ferrets.

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
NS1 position 200; NS1 position 205
Mechanism types
immune_escape; pathogenicity
1 records
Extraction confidence 0.88
Key finding

Experimental infection of ferrets showed that human-origin H5N1 influenza virus strain UT3062 was highly virulent while UT3028 was avirulent; reassortant viruses demonstrated that HA and NS genes govern virulence differences in ferrets.

Virus
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. We then generated a series of reassortant viruses between the two viruses and assessed their virulence in ferrets.

Method
experimental infection; virulence assay; reassortant virus generation
Experimental system
in vivo animal experiment
1 records
Extraction confidence 0.90
Key finding

An amino acid substitution at position 134 of the H5N1 HA protein changed the receptor‑binding property of the virus.

Virus
Location
Not specified
Supporting text

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.

Method
viral elution assay
Receptors
hemagglutinin (HA) receptor-binding property
1 records
Extraction confidence 0.80
Key finding

Reassortant H5N1 viruses containing HA and NS segments from the virulent A/Vietnam/UT3062/04 strain were highly virulent in ferrets, indicating that reassortment of these genes confers increased pathogenicity.

Host
Not specified
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.

Event type
reassortment
Genes or segments
HA; NS