Literature detail

Investigation of influenza virus polymerase activity in pig cells.

Olivier Moncorgé1 Jason S Long Anna V Cauldwell Hongbo Zhou Samantha J Lycett Wendy S Barclay
Affiliations 1 institutions
  1. Section of Virology, Department of Medicine, Imperial College London, St. Mary's Campus, London, United Kingdom.
PMID 23077313 2013 J Virol eng ppublish
PubMed DOI Browse context

Article

Publication summary

Reassortant influenza viruses with combinations of avian, human, and/or swine genomic segments have been detected frequently in pigs. As a consequence, pigs have been accused of being a "mixing vessel" for influenza viruses. This implies that pig cells support transcription and replication of avian influenza viruses, in contrast to human cells, in which most avian influenza virus polymerases display limited activity. Although influenza virus polymerase activity has been studied in human and avian cells for many years by use of a minigenome assay, similar investigations in pig cells have not been reported. We developed the first minigenome assay for pig cells and compared the activities of polymerases of avian or human influenza virus origin in pig, human, and avian cells. We also investigated in pig cells the consequences of some known mammalian host range determinants that enhance influenza virus polymerase activity in human cells, such as PB2 mutations E627K, D701N, G590S/Q591R, and T271A. The two typical avian influenza virus polymerases used in this study were poorly active in pig cells, similar to what is seen in human cells, and mutations that adapt the avian influenza virus polymerase for human cells also increased activity in pig cells. In contrast, a different pattern was observed in avian cells. Finally, highly pathogenic avian influenza virus H5N1 polymerase activity was tested because this subtype has been reported to replicate only poorly in pigs. H5N1 polymerase was active in swine cells, suggesting that other barriers restrict these viruses from becoming endemic in pigs.

Animals Cells, Cultured Influenza A virus Mutant Proteins Mutation, Missense RNA-Dependent RNA Polymerase Swine Virus Replication

Structured evidence records

Evidence records

3 total
2 records
Extraction confidence 0.90
Key finding

Avian influenza virus polymerase showed limited activity in pig cells, which increased with human-adaptive PB2 mutations indicating restricted but adaptable replication capacity.

Virus
Location
Not specified
Supporting text

We developed the first minigenome assay for pig cells and compared the activities of polymerases of avian or human influenza virus origin in pig, human, and avian cells. The two typical avian influenza virus polymerases used in this study were poorly active in pig cells, similar to what is seen in human cells, and mutations that adapt the avian influenza virus polymerase for human cells also increased activity in pig cells.

Method
minigenome assay; polymerase activity assay
Experimental system
in vitro cell culture
Extraction confidence 0.90
Key finding

H5N1 polymerase exhibited measurable activity in swine cells, indicating pig cells can support replication-associated functions despite other non-polymerase barriers.

Virus
Location
Not specified
Supporting text

Finally, highly pathogenic avian influenza virus H5N1 polymerase activity was tested because this subtype has been reported to replicate only poorly in pigs. H5N1 polymerase was active in swine cells, suggesting that other barriers restrict these viruses from becoming endemic in pigs.

Method
polymerase activity assay
Experimental system
in vitro cell culture
1 records
Extraction confidence 0.95
Key finding

PB2 mutations E627K, D701N, G590S/Q591R, and T271A enhanced avian influenza virus polymerase activity in pig cells, indicating mammalian adaptation of the avian polymerase.

Virus
Host
Not specified
Location
Not specified
Supporting text

Mutations that adapt the avian influenza virus polymerase for human cells, such as PB2 E627K, D701N, G590S/Q591R, and T271A, also increased activity in pig cells.

Genes or proteins
PB2; polymerase
Mutations
PB2 E627K; PB2 D701N; PB2 G590S/Q591R; PB2 T271A
Mechanism types
polymerase_activity; host_adaptation