Format

Send to

Choose Destination
Sci Rep. 2016 Mar 18;6:23138. doi: 10.1038/srep23138.

Influenza A viruses escape from MxA restriction at the expense of efficient nuclear vRNP import.

Author information

1
Institute of Virology, University Medical Center Freiburg, D-79104 Freiburg, Germany.
2
Institute of Diagnostic Virology, Friedrich-Loeffler-Institute, 17493 Greifswald-Insel Riems, Germany.
3
Center of Excellence for Poultry Science, University of Arkansas, Fayetteville, AR 72701, USA.
4
Nuclear Signaling Laboratory, Department of Biochemistry and Molecular Biology, Monash University, Melbourne, Victoria, Australia.

Abstract

To establish a new lineage in the human population, avian influenza A viruses (AIV) must overcome the intracellular restriction factor MxA. Partial escape from MxA restriction can be achieved when the viral nucleoprotein (NP) acquires the critical human-adaptive amino acid residues 100I/V, 283P, and 313Y. Here, we show that introduction of these three residues into the NP of an avian H5N1 virus renders it genetically unstable, resulting in viruses harboring additional single mutations, including G16D. These substitutions restored genetic stability yet again yielded viruses with varying degrees of attenuation in mammalian and avian cells. Additionally, most of the mutant viruses lost the capacity to escape MxA restriction, with the exception of the G16D virus. We show that MxA escape is linked to attenuation by demonstrating that the three substitutions promoting MxA escape disturbed intracellular trafficking of incoming viral ribonucleoprotein complexes (vRNPs), thereby resulting in impaired nuclear import, and that the additional acquired mutations only partially compensate for this import block. We conclude that for adaptation to the human host, AIV must not only overcome MxA restriction but also an associated block in nuclear vRNP import. This inherent difficulty may partially explain the frequent failure of AIV to become pandemic.

PMID:
26988202
PMCID:
PMC4796820
DOI:
10.1038/srep23138
[Indexed for MEDLINE]
Free PMC Article

Supplemental Content

Full text links

Icon for Nature Publishing Group Icon for PubMed Central
Loading ...
Support Center