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.

Abstract

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.

Supporting text Virus Host Location
Virus Replication 191 Amino Acid Substitution 81 Animals 1948 Cell Line 158 Dogs 176 Influenza A Virus, H1N1 Subtype 74 Influenza A Virus, H5N1 Subtype 300 Mutation, Missense 26 Orthomyxoviridae Infections 228 Reassortant Viruses 103 RNA-Dependent RNA Polymerase 49 Sequence Analysis, DNA 113 Swine 258 Viral Proteins 152 PB2 protein, Influenzavirus A 27

Evidence records

2 total
Zoonotic Surveillance
1 records · 1 evidence types
Evidence type
1 records
OVE632
Key finding

Two infectious reassortant H5N1 virus clones were recovered from experimentally infected pigs, demonstrating successful virus isolation after infection.

Virus
Host
Location
Not specified
Supporting text

Two in vivo-generated single-gene reassortant virus clones of the H5N1 subtype (virus clones 1 and 2)... were recovered from the experimentally infected pigs.

Sample type
respiratory tract samples | animal tissues (experimentally infected pigs)
Functional Mechanism
1 records · 1 evidence types
Evidence type
1 records
OVE633
Key finding

PB2 mutations D256G and E627K in the reassortant H5N1 virus rg-Sw-Ck/PB2 enhance viral polymerase activity and replication in pigs, indicating mammalian adaptation.

Virus
Host
Not specified
Location
Not specified
Supporting text

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.

Genes or proteins
PB2
Mutations
D256G | E627K
Mechanism types
replication adaptation | host-range expansion