Abstract

Influenza A virus nucleoprotein, is a multifunctional RNA-binding protein, encoded by segment-5 of the negative sense RNA genome. It serves as a key connector between the virus and the host during virus replication. It continuously shuttles between the cytoplasm and the nucleus interacting with various host cellular factors. In the current study, host proteins interacting with nucleoprotein of Influenza A virus of H1N1 2009 pandemic strain were identified by co-immunoprecipitation studies followed by MALDI-TOF/MS analysis. Here we report the host nucleolin, a major RNA-binding protein of the nucleolus as a novel interacting partner to influenza A virus nucleoprotein. We thus, explored the implications of this interaction in virus life cycle and our studies have shown that these two proteins interact early during infection in the cytoplasm of infected cells. Depletion of nucleolin in A549 cells by siRNA targeting endogenous nucleolin followed by influenza A virus infection, disrupted its interaction with viral nucleoprotein, resulting in increased expression of gene transcripts encoding late viral proteins; matrix (M1) and hemagglutinin (HA) in infected cells. On the contrary, over expression of nucleolin in cells transiently transfected with pEGFP-NCL construct followed by virus infection significantly reduced the late viral gene transcripts, and consequently the viral titer. Altered expression of late viral genes and titers following manipulation of host cellular nucleolin, proposes the functional importance of its interaction with nucleoprotein during influenza A virus infection.

Highlights

  • Influenza A virus is a public health threat worldwide and contributes to a high-level of mortality during pandemics

  • Our results demonstrate that the host nucleolin interaction with viral NP reduces the viral titer by limiting the transcription of late viral genes

  • Identification of host cellular proteins interacting with influenza A virus nucleoprotein

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Summary

Introduction

Influenza A virus is a public health threat worldwide and contributes to a high-level of mortality during pandemics. Host Nucleolin and Virus Nucleoprotein Interaction influenza A virus encode for 10 proteins. 7 more novel proteins; PB1-F2 [1], PB1-N40 [2], PA-N155, PA-N182 [3], PA-X [4], M42 [5] and NS3 [6] were discovered 40years after the genome mapping of influenza A virus was done. NP determines whether complementary RNA, synthesized from genomic RNA, is to be used for protein translation or to serve as a template for synthesis of genomic strand during the replication [9]. Besides its active role in the replication of virus, NP contributes to host adaptation when avian strains change their host to mammalian species. Mutations in NP together with subunits of RNA polymerase contribute to increased polymerase activity of avian strains [10]. All the above reports together signify the indispensable role of NP in influenza A virus life cycle

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