Literature detail

PB2 protein of a highly pathogenic avian influenza virus strain A/chicken/Yamaguchi/7/2004 (H5N1) determines its replication potential in pigs.

Rashid Manzoor1 Yoshihiro Sakoda Naoki Nomura Yoshimi Tsuda Hiroichi Ozaki Masatoshi Okamatsu Hiroshi Kida
Affiliations 1 institutions
  1. Department of Disease Control, Graduate School of Veterinary Medicine, Hokkaido University, Sapporo, Japan.
PMID 19052090 2009 J Virol eng ppublish
PubMed DOI Browse context

Article

Publication summary

It has been shown that not all but most of the avian influenza viruses replicate in the upper respiratory tract of pigs (H. Kida et al., J. Gen. Virol. 75:2183-2188, 1994). It was shown that A/chicken/Yamaguchi/7/2004 (H5N1) [Ck/Yamaguchi/04 (H5N1)] did not replicate in pigs (N. Isoda et al., Arch. Virol. 151:1267-1279, 2006). In the present study, the genetic basis for this host range restriction was determined using reassortant viruses generated between Ck/Yamaguchi/04 (H5N1) and A/swine/Hokkaido/2/1981 (H1N1) [Sw/Hokkaido/81 (H1N1)]. Two in vivo-generated single-gene reassortant virus clones of the H5N1 subtype (virus clones 1 and 2), whose PB2 gene was of Sw/Hokkaido/81 (H1N1) origin and whose remaining seven genes were of Ck/Yamaguchi/04 (H5N1) origin, were recovered from the experimentally infected pigs. The replicative potential of virus clones 1 and 2 was further confirmed by using reassortant virus (rg-Ck-Sw/PB2) generated by reverse genetics. Interestingly, the PB2 gene of Ck/Yamaguchi/04 (H5N1) did not restrict the replication of Sw/Hokkaido/81 (H1N1), as determined by using reassortant virus rg-Sw-Ck/PB2. The rg-Sw-Ck/PB2 virus replicated to moderate levels and for a shorter duration than parental Sw/Hokkaido/81 (H1N1). Sequencing of two isolates recovered from the pigs inoculated with rg-Sw-Ck/PB2 revealed either the D256G or the E627K amino acid substitution in the PB2 proteins of the isolates. The D256G and E627K mutations enhanced viral polymerase activity in the mammalian cells, correlating with replication of virus in pigs. These results indicate that the PB2 protein restricts the growth of Ck/Yamaguchi/04 (H5N1) in pigs.

Virus Replication Amino Acid Substitution Animals Cell Line Dogs Influenza A Virus, H1N1 Subtype Influenza A Virus, H5N1 Subtype Mutation, Missense Orthomyxoviridae Infections Reassortant Viruses RNA-Dependent RNA Polymerase Sequence Analysis, DNA Swine Viral Proteins PB2 protein, Influenzavirus A

Structured evidence records

Evidence records

4 total
1 records
Extraction confidence 0.85
Key finding

Avian influenza virus A/chicken/Yamaguchi/7/2004 (H5N1) acquired replication potential in pigs via PB2 reassortment with swine influenza virus A/swine/Hokkaido/2/1981 (H1N1).

Virus
Location
Supporting text

Two in vivo-generated single-gene reassortant virus clones of the H5N1 subtype, whose PB2 gene was of Sw/Hokkaido/81 (H1N1) origin and whose remaining seven genes were of Ck/Yamaguchi/04 (H5N1) origin, were recovered from the experimentally infected pigs.

Method
experimental infection; reassortant virus generation; sequencing
Study design
animal experiment
Transmission direction
animal-to-animal
Geographic raw
Hokkaido, Yamaguchi
Country inferred
Japan
1 records
Extraction confidence 0.95
Key finding

Reassortant H5N1 influenza viruses carrying the PB2 gene from A/swine/Hokkaido/2/1981 (H1N1) replicated in pigs, demonstrating that PB2 determines replication potential in this host.

Virus
Location
Not specified
Supporting text

Two in vivo-generated single-gene reassortant virus clones of the H5N1 subtype, whose PB2 gene was of Sw/Hokkaido/81 (H1N1) origin, were recovered from the experimentally infected pigs. The replicative potential of virus clones 1 and 2 was further confirmed by using reassortant virus generated by reverse genetics.

Method
experimental infection; reverse genetics; virus recovery
Sample type
upper respiratory tract
Experimental system
in vivo animal experiment
1 records
Extraction confidence 0.95
Key finding

D256G and E627K substitutions in the PB2 protein of H5N1 enhanced polymerase activity and supported replication in pigs, indicating molecular adaptation for mammalian replication.

Virus
Host
Not specified
Location
Not specified
Supporting text

Sequencing of two isolates recovered from pigs inoculated with rg-Sw-Ck/PB2 revealed either the D256G or the E627K amino acid substitution in the PB2 proteins of the isolates. The D256G and E627K mutations enhanced viral polymerase activity in mammalian cells, correlating with replication of virus in pigs.

Genes or proteins
PB2
Mutations
D256G; E627K
Mechanism types
polymerase_activity; replication_efficiency
1 records
Extraction confidence 0.90
Key finding

Reassortant H5N1 viruses carrying the PB2 gene from swine H1N1 replicated in pigs, demonstrating that PB2 reassortment can expand avian influenza virus host range to pigs.

Host
Not specified
Location
Not specified
Supporting text

In the present study, the genetic basis for this host range restriction was determined using reassortant viruses generated between Ck/Yamaguchi/04 (H5N1) and A/swine/Hokkaido/2/1981 (H1N1). Two in vivo-generated single-gene reassortant virus clones of the H5N1 subtype, whose PB2 gene was of Sw/Hokkaido/81 (H1N1) origin and whose remaining seven genes were of Ck/Yamaguchi/04 (H5N1) origin, were recovered from the experimentally infected pigs.

Event type
reassortment
Genes or segments
PB2