Abstract

Influenza A viruses may cross species barriers and transmit to humans with the potential to cause pandemics. Interplay of human- (PB2 627K) and avian-like (PB2 627E) influenza polymerase complexes with unknown host factors have been postulated to play a key role in interspecies transmission. Here, we have identified human importin-α isoforms (α1 and α7) as positive regulators of human- but not avian-like polymerase activity. Human-like polymerase activity correlated with efficient recruitment of α1 and α7 to viral ribonucleoprotein complexes (vRNPs) without affecting subcellular localization. We also observed that human-like influenza virus growth was impaired in α1 and α7 downregulated human lung cells. Mice lacking α7 were less susceptible to human- but not avian-like influenza virus infection. Thus, α1 and α7 are positive regulators of human-like polymerase activity and pathogenicity beyond their role in nuclear transport.

Highlights

  • Influenza A viruses are able to cross species barriers and transmit to humans leading to disease of various severity

  • Human-like polymerase activity depends on importin-a1 and -a7 in human cells

  • It has been proposed that avian-like polymerase complexes containing PB2 627E are restricted by an unknown host factor which is only present in a mammalian host environment [11]

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Summary

Introduction

Influenza A viruses are able to cross species barriers and transmit to humans leading to disease of various severity. Interspecies transmission of influenza viruses is multigenic involving several viral and cellular factors. Host restriction occurs mainly by two cellular barriers which need to be overcome upon transmission. Upon entry viruses need to cross the cell membrane by interaction of the viral receptor binding protein, the hemagglutinin (HA), to the adequate host cell receptors consisting of sialic acid-containing glycoproteins [1,2]. The adaptive position in the viral polymerase subunit PB2 at position 627 is a well known determinant of host range and pathogenicity [6]. The PB2 E627K mutation has been shown to increase viral polymerase activity [3] and pathogenicity in mammalian hosts [8,9]

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