Host-Specific Restriction of Avian Influenza Virus Caused by Differential Dynamics of ANP32 Family Members

J Infect Dis. 2020 Jan 1;221(1):71-80. doi: 10.1093/infdis/jiz506.

Abstract

Background: Influenza viruses must utilize host factors to complete their lifecycle. Species-specific differences in host factors between birds and mammals mean that avian influenza viruses (AIVs) replicate well in avian hosts but not in human hosts. Acidic nuclear phosphoprotein 32 family member A (ANP32A) has been identified as the host restriction factor for the viral polymerase (vPol) activity of AIVs. The ANP32A belongs to the conserved ANP32 family, the functional roles of which during viral replication remain unclear.

Methods: In this study, we targeted chicken ANP32A using clustered regularly interspaced short palindromic repeats (CRISPR)/Cas9-mediated genome editing to examine the functional roles of ANP32A and other members of the ANP32 family.

Results: We showed that chicken ANP32A only, not ANP32B and ANP32E, plays a pivotal role in supporting vPol activity of AIVs. Furthermore, we found that the human ANP32C, ANP32D, and ANP32E have suppressive effects on vPol activity in contrast to human ANP32A and ANP32B.

Conclusions: Chicken and human ANP32 family members had different effects on vPol activity, suggesting that species-specific vPol activity of AIVs could be caused by the differential functions and overall competency of ANP32 family members.

Keywords: ANP32 family; cellular host factor; host restriction; influenza virus.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Chickens
  • DNA-Directed RNA Polymerases / metabolism*
  • Dogs
  • Gene Knockdown Techniques
  • Influenza A virus / enzymology*
  • Influenza in Birds / enzymology
  • Influenza in Birds / genetics*
  • Intercellular Signaling Peptides and Proteins / genetics
  • Intercellular Signaling Peptides and Proteins / metabolism*
  • Intracellular Signaling Peptides and Proteins
  • Madin Darby Canine Kidney Cells
  • Molecular Chaperones / genetics
  • Molecular Chaperones / metabolism
  • Nuclear Proteins / genetics*
  • Nuclear Proteins / metabolism
  • Phosphoproteins / genetics
  • Phosphoproteins / metabolism
  • RNA-Binding Proteins / genetics*
  • RNA-Binding Proteins / metabolism
  • Sequence Analysis, DNA
  • Virus Replication / genetics*

Substances

  • ANP32A protein, human
  • ANP32B protein, human
  • ANP32C protein, human
  • ANP32D protein, human
  • ANP32E protein, human
  • Intercellular Signaling Peptides and Proteins
  • Intracellular Signaling Peptides and Proteins
  • Molecular Chaperones
  • Nuclear Proteins
  • Phosphoproteins
  • RNA-Binding Proteins
  • DNA-Directed RNA Polymerases