The Cellular Factor NXP2/MORC3 Is a Positive Regulator of Influenza Virus Multiplication

Lorena S Ver1, Laura Marcos-Villar1, Sara Landeras-Bueno1

  • 1Centro Nacional de Biotecnología (CSIC), Darwin 3, Madrid, Spain CIBER de Enfermedades Respiratorias, ISCIII, Madrid, Spain.

Journal of Virology
|July 24, 2015
PubMed
Abstract

Insights

The cellular protein NXP2/MORC3 associates with influenza A virus components, aiding viral transcription. Downregulating NXP2/MORC3 reduces viral RNA and protein production, highlighting its role in the virus life cycle.

Area of Science:

  • Virology
  • Molecular Biology
  • Cell Biology

Background:

  • Influenza A virus (IAV) replication and transcription occur in the host cell nucleus, involving viral ribonucleoproteins (RNPs) and a complex viral polymerase.
  • Host cell factors play a critical role in the IAV life cycle, interacting with viral components.
  • NXP2/MORC3, a nuclear matrix-associated protein with RNA-binding activity, belongs to the Microrchidia (MORC) family.

Purpose of the Study:

  • To investigate the role of the host cell protein NXP2/MORC3 in the influenza A virus infection cycle.
  • To determine the association of NXP2/MORC3 with viral components during infection.
  • To assess the impact of NXP2/MORC3 on viral replication and transcription.

Main Methods:

  • Proteomic analysis to identify polymerase-associated cellular proteins.
  • Coimmunoprecipitation and immunofluorescence to confirm protein-protein interactions and localization.
  • Short hairpin RNA (shRNA)-mediated knockdown to downregulate NXP2/MORC3 expression.
  • Analysis of viral titers, viral RNA (vRNA), and mRNA levels.
  • Use of a recombinant influenza virus CAT minireplicon system.

Main Results:

  • Influenza virus infection caused a slight increase in NXP2/MORC3 expression and partial cytoplasmic relocalization.
  • NXP2/MORC3 was found to associate with the viral polymerase and RNPs in infected cells.
  • Downregulation of NXP2/MORC3 led to reduced virus titers and decreased accumulation of viral RNA and mRNA.
  • In a minireplicon system, NXP2/MORC3 silencing reduced viral mRNA and protein but not vRNA levels.

Conclusions:

  • NXP2/MORC3 is a host factor that associates with influenza A virus polymerase and RNPs.
  • NXP2/MORC3 plays a significant role in influenza virus transcription.
  • NXP2/MORC3 is important for efficient viral replication and production.

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