Influenza A Virus Nucleoprotein Exploits Hsp40 to Inhibit PKR Activation

Background Double-stranded RNA dependent protein kinase (PKR) is a key regulator of the anti-viral innate immune response in mammalian cells. PKR activity is regulated by a 58 kilo Dalton cellular inhibitor (P58IPK), which is present in inactive state as a complex with Hsp40 under normal conditions. In case of influenza A virus (IAV) infection, P58IPK is known to dissociate from Hsp40 and inhibit PKR activation. However the influenza virus component responsible for PKR inhibition through P58IPK activation was hitherto unknown. Principal Findings Human heat shock 40 protein (Hsp40) was identified as an interacting partner of Influenza A virus nucleoprotein (IAV NP) using a yeast two-hybrid screen. This interaction was confirmed by co-immunoprecipitation studies from mammalian cells transfected with IAV NP expressing plasmid. Further, the IAV NP-Hsp40 interaction was validated in mammalian cells infected with various seasonal and pandemic strains of influenza viruses. Cellular localization studies showed that NP and Hsp40 co-localize primarily in the nucleus. During IAV infection in mammalian cells, expression of NP coincided with the dissociation of P58IPK from Hsp40 and decrease PKR phosphorylation. We observed that, plasmid based expression of NP in mammalian cells leads to decrease in PKR phosphorylation. Furthermore, inhibition of NP expression during influenza virus replication led to PKR activation and concomitant increase in eIF2α phosphorylation. Inhibition of NP expression also led to reduced IRF3 phosphorylation, enhanced IFN β production and concomitant reduction of virus replication. Taken together our data suggest that NP is the viral factor responsible for P58IPK activation and subsequent inhibition of PKR-mediated host response during IAV infection. Significance Our findings demonstrate a novel role of IAV NP in inhibiting PKR-mediated anti-viral host response and help us understand P58IPK mediated inhibition of PKR activity during IAV infection.

[1]  J. M. Cameron,et al.  Inhibition of PKR by RNA and DNA viruses. , 2006, Virus research.

[2]  M. Nei,et al.  MEGA4: Molecular Evolutionary Genetics Analysis (MEGA) software version 4.0. , 2007, Molecular biology and evolution.

[3]  Amer A. Beg,et al.  Influenza A Virus NS1 Protein Prevents Activation of NF-κB and Induction of Alpha/Beta Interferon , 2000, Journal of Virology.

[4]  Robert E. O'Neill,et al.  Cellular Splicing Factor RAF-2p48/NPI-5/BAT1/UAP56 Interacts with the Influenza Virus Nucleoprotein and Enhances Viral RNA Synthesis , 2001, Journal of Virology.

[5]  G. Gao,et al.  Interaction of Hsp40 with influenza virus M2 protein: implications for PKR signaling pathway , 2010, Protein & Cell.

[6]  B. Williams,et al.  Protein Kinase R (PKR) Interacts with and Activates Mitogen-activated Protein Kinase Kinase 6 (MKK6) in Response to Double-stranded RNA Stimulation* , 2004, Journal of Biological Chemistry.

[7]  A. Kawaguchi,et al.  Involvement of Hsp90 in Assembly and Nuclear Import of Influenza Virus RNA Polymerase Subunits , 2006, Journal of Virology.

[8]  Jingzhi Li,et al.  Heat shock protein 40: structural studies and their functional implications. , 2009, Protein and peptide letters.

[9]  M. Katze,et al.  Binding of the influenza virus NS1 protein to double-stranded RNA inhibits the activation of the protein kinase that phosphorylates the elF-2 translation initiation factor. , 1995, Virology.

[10]  Michael G. Katze,et al.  The Cellular Protein P58IPK Regulates Influenza Virus mRNA Translation and Replication through a PKR-Mediated Mechanism , 2006, Journal of Virology.

[11]  E. Meurs,et al.  PKR Stimulates NF-κB Irrespective of Its Kinase Function by Interacting with the IκB Kinase Complex , 2000, Molecular and Cellular Biology.

[12]  Adolfo Garcia-Sastre,et al.  Influenza Virus NS1 Protein Counteracts PKR-Mediated Inhibition of Replication , 2000, Journal of Virology.

[13]  服部 浩朋 A stress-inducible 40 kDa protein (hsp40) : purification by modified two-dimensional gel electrophoresis and co-localization with hsc70(p73) in heat-shocked HeLa cells , 1993 .

[14]  Matthew D. Dyer,et al.  P58IPK: A Novel “CIHD” Member of the Host Innate Defense Response against Pathogenic Virus Infection , 2009, PLoS pathogens.

[15]  C. Garrido,et al.  Dual Role of Heat Shock Proteins as Regulators of Apoptosis and Innate Immunity , 2010, Journal of Innate Immunity.

[16]  J. Hiscott,et al.  Multiple signaling pathways leading to the activation of interferon regulatory factor 3. , 2002, Biochemical pharmacology.

[17]  M. Katze,et al.  The molecular chaperone hsp40 regulates the activity of P58IPK, the cellular inhibitor of PKR. , 1997, Proceedings of the National Academy of Sciences of the United States of America.

[18]  P. Shaw,et al.  Structure and sequence analysis of influenza A virus nucleoprotein , 2009, Science in China Series C: Life Sciences.

[19]  M. Cheetham,et al.  Structure, function and evolution of DnaJ: conservation and adaptation of chaperone function. , 1998, Cell stress & chaperones.

[20]  R. Lamb,et al.  Orthomyxoviridae: The Viruses and Their Replication. , 1996 .

[21]  Yoshihiro Kawaoka,et al.  Cellular networks involved in the influenza virus life cycle. , 2010, Cell host & microbe.

[22]  G. Poland,et al.  H5N1 Avian influenza: preventive and therapeutic strategies against a pandemic. , 2010, Annual review of medicine.

[23]  Masaki Hata,et al.  Molecular chaperone function of mammalian Hsp70 and Hsp40-a review , 2000, International journal of hyperthermia : the official journal of European Society for Hyperthermic Oncology, North American Hyperthermia Group.

[24]  M. Katze,et al.  Constitutive expression of human double-stranded RNA-activated p68 kinase in murine cells mediates phosphorylation of eukaryotic initiation factor 2 and partial resistance to encephalomyocarditis virus growth , 1992, Journal of Virology.

[25]  V. Chow,et al.  The nucleocapsid protein of the SARS coronavirus is capable of self-association through a C-terminal 209 amino acid interaction domain , 2004, Biochemical and Biophysical Research Communications.

[26]  A. García-Sastre,et al.  The NS1 Protein of a Human Influenza Virus Inhibits Type I Interferon Production and the Induction of Antiviral Responses in Primary Human Dendritic and Respiratory Epithelial Cells , 2009, Journal of Virology.

[27]  M. Katze,et al.  Double-Stranded RNA-Independent Dimerization of Interferon-Induced Protein Kinase PKR and Inhibition of Dimerization by the Cellular P58IPK Inhibitor , 1998, Molecular and Cellular Biology.

[28]  B. Ahn,et al.  Turnover of hepatitis B virus X protein is facilitated by Hdj1, a human Hsp40/DnaJ protein. , 2006, Biochemical and biophysical research communications.

[29]  T. Fujita,et al.  NS1 protein of influenza A virus inhibits the function of intracytoplasmic pathogen sensor, RIG-I. , 2007, American journal of respiratory cell and molecular biology.

[30]  J. McCauley,et al.  Edinburgh Research Explorer Interaction of the influenza virus nucleoprotein with the cellular CRM1-mediated nuclear export pathway , 2022 .

[31]  M. Katze,et al.  The P58 Cellular Inhibitor Complexes with the Interferon-induced, Double-stranded RNA-dependent Protein Kinase, PKR, to Regulate Its Autophosphorylation and Activity (*) , 1996, The Journal of Biological Chemistry.

[32]  A. Kar-Roy,et al.  The ORF3 protein of hepatitis E virus interacts with hemopexin by means of its 26 amino acid N-terminal hydrophobic domain II. , 2008, Biochemistry.

[33]  R. Krug,et al.  The mechanism by which influenza A virus nucleoprotein forms oligomers and binds RNA , 2006, Nature.

[34]  M. Katze,et al.  Cellular inhibitors of the interferon-induced, dsRNA-activated protein kinase. , 1994, Progress in molecular and subcellular biology.

[35]  M. Katze,et al.  Molecular mechanisms of interferon resistance mediated by viral-directed inhibition of PKR, the interferon-induced protein kinase. , 1998, Pharmacology & therapeutics.

[36]  James M Aramini,et al.  Structures of influenza A proteins and insights into antiviral drug targets , 2010, Nature Structural &Molecular Biology.

[37]  E. Meurs,et al.  The dsRNA protein kinase PKR: virus and cell control. , 2007, Biochimie.

[38]  Manish Kumar,et al.  Heat Shock Protein 40 Is Necessary for Human Immunodeficiency Virus-1 Nef-mediated Enhancement of Viral Gene Expression and Replication* , 2005, Journal of Biological Chemistry.

[39]  D. Levy,et al.  IRF3 and IRF7 Phosphorylation in Virus-infected Cells Does Not Require Double-stranded RNA-dependent Protein Kinase R or IκB Kinase but Is Blocked by Vaccinia Virus E3L Protein* , 2001, The Journal of Biological Chemistry.

[40]  P. Digard,et al.  The influenza virus nucleoprotein: a multifunctional RNA-binding protein pivotal to virus replication. , 2002, The Journal of general virology.

[41]  Michael T. McManus,et al.  RNA interference of influenza virus production by directly targeting mRNA for degradation and indirectly inhibiting all viral RNA transcription , 2003, Proceedings of the National Academy of Sciences of the United States of America.

[42]  G. Kochs,et al.  Inverse interference: how viruses fight the interferon system. , 2004, Viral immunology.

[43]  P. L. Boutz,et al.  Influenza Virus Nucleoprotein Interacts with Influenza Virus Polymerase Proteins , 1998, Journal of Virology.

[44]  M. Katze,et al.  Influenza virus regulates protein synthesis during infection by repressing autophosphorylation and activity of the cellular 68,000-Mr protein kinase , 1988, Journal of virology.

[45]  L. Ratner,et al.  Hsp40 Facilitates Nuclear Import of the Human Immunodeficiency Virus Type 2 Vpx-Mediated Preintegration Complex , 2007, Journal of Virology.

[46]  J. Connor,et al.  Inhibition of Host and Viral Translation during Vesicular Stomatitis Virus Infection , 2005, Journal of Biological Chemistry.

[47]  Wenjun Song,et al.  Nuclear Factor 90 Negatively Regulates Influenza Virus Replication by Interacting with Viral Nucleoprotein , 2009, Journal of Virology.

[48]  S. Miao,et al.  The diversity of the DnaJ/Hsp40 family, the crucial partners for Hsp70 chaperones , 2006, Cellular and Molecular Life Sciences CMLS.

[49]  Etsuko Hirayama,et al.  Heat Shock Protein 70 Is Related to Thermal Inhibition of Nuclear Export of the Influenza Virus Ribonucleoprotein Complex , 2004, Journal of Virology.

[50]  I. Kerr,et al.  Molecular cloning and characterization of the human double-stranded RNA-activated protein kinase induced by interferon , 1990, Cell.

[51]  H. Klenk,et al.  Interaction of Polymerase Subunit PB2 and NP with Importin α1 Is a Determinant of Host Range of Influenza A Virus , 2008, PLoS pathogens.

[52]  P. Ranjan,et al.  Cytoplasmic nucleic acid sensors in antiviral immunity. , 2009, Trends in molecular medicine.

[53]  T. Anthony,et al.  Coping with stress: eIF2 kinases and translational control. , 2006, Biochemical Society transactions.