A Novel Single Virus Infection System Reveals That Influenza Virus Preferentially Infects Cells in G1 Phase

Background Influenza virus attaches to sialic acid residues on the surface of host cells via the hemagglutinin (HA), a glycoprotein expressed on the viral envelope, and enters into the cytoplasm by receptor-mediated endocytosis. The viral genome is released and transported in to the nucleus, where transcription and replication take place. However, cellular factors affecting the influenza virus infection such as the cell cycle remain uncharacterized. Methods/Results To resolve the influence of cell cycle on influenza virus infection, we performed a single-virus infection analysis using optical tweezers. Using this newly developed single-virus infection system, the fluorescence-labeled influenza virus was trapped on a microchip using a laser (1064 nm) at 0.6 W, transported, and released onto individual H292 human lung epithelial cells. Interestingly, the influenza virus attached selectively to cells in the G1-phase. To clarify the molecular differences between cells in G1- and S/G2/M-phase, we performed several physical and chemical assays. Results indicated that: 1) the membranes of cells in G1-phase contained greater amounts of sialic acids (glycoproteins) than the membranes of cells in S/G2/M-phase; 2) the membrane stiffness of cells in S/G2/M-phase is more rigid than those in G1-phase by measurement using optical tweezers; and 3) S/G2/M-phase cells contained higher content of Gb3, Gb4 and GlcCer than G1-phase cells by an assay for lipid composition. Conclusions A novel single-virus infection system was developed to characterize the difference in influenza virus susceptibility between G1- and S/G2/M-phase cells. Differences in virus binding specificity were associated with alterations in the lipid composition, sialic acid content, and membrane stiffness. This single-virus infection system will be useful for studying the infection mechanisms of other viruses.

[1]  C. Ward,et al.  Structure of the influenza virus hemagglutinin. , 1981, Current topics in microbiology and immunology.

[2]  R. Webster,et al.  Receptor specificity in human, avian, and equine H2 and H3 influenza virus isolates. , 1994, Virology.

[3]  E. Jost,et al.  Molecular cloning of a murine cDNA encoding a novel protein, p38-2G4, which varies with the cell cycle. , 1995, Experimental cell research.

[4]  D E Ingber,et al.  Cell shape, cytoskeletal mechanics, and cell cycle control in angiogenesis. , 1995, Journal of biomechanics.

[5]  Y. Yasukochi,et al.  Cell cycle-dependent regulation of RNA polymerase II basal transcription activity. , 1995, Nucleic acids research.

[6]  S. Ishiwata,et al.  Preparation of bead-tailed actin filaments: estimation of the torque produced by the sliding force in an in vitro motility assay. , 1996, Biophysical journal.

[7]  Michelle D. Wang,et al.  Stretching DNA with optical tweezers. , 1997, Biophysical journal.

[8]  M. Roth,et al.  A point mutation in the transmembrane domain of the hemagglutinin of influenza virus stabilizes a hemifusion intermediate that can transit to fusion. , 2000, Molecular biology of the cell.

[9]  X. W. Wang,et al.  Interaction of the PA2G4 (EBP1) protein with ErbB-3 and regulation of this binding by heregulin , 2000, British Journal of Cancer.

[10]  A. Hamburger,et al.  Ebp1, an ErbB‐3 binding protein, interacts with Rb and affects Rb transcriptional regulation , 2001, Journal of cellular physiology.

[11]  Ayae Honda,et al.  Minimum molecular architectures for transcription and replication of the influenza virus , 2002, Proceedings of the National Academy of Sciences of the United States of America.

[12]  Qianben Wang,et al.  Repression of androgen receptor mediated transcription by the ErbB-3 binding protein, Ebp1 , 2002, Oncogene.

[13]  A. Hamburger,et al.  Repression of E2F1-mediated transcription by the ErbB3 binding protein Ebp1 involves histone deacetylases. , 2003, Nucleic acids research.

[14]  R. Krug,et al.  Crucial role of CA cleavage sites in the cap‐snatching mechanism for initiating viral mRNA synthesis , 2003, The EMBO journal.

[15]  Michael J Rust,et al.  Endocytosis of influenza viruses. , 2004, Microbes and infection.

[16]  Feng Zhang,et al.  Assembly of endocytic machinery around individual influenza viruses during viral entry , 2004, Nature Structural &Molecular Biology.

[17]  N. Cozzarelli,et al.  The Bacterial Condensin MukBEF Compacts DNA into a Repetitive, Stable Structure , 2004, Science.

[18]  A. Hamburger,et al.  The ErbB3-binding protein Ebp1 suppresses androgen receptor-mediated gene transcription and tumorigenesis of prostate cancer cells. , 2005, Proceedings of the National Academy of Sciences of the United States of America.

[19]  Fumihito Arai,et al.  In-situ formation of a gel microbead for laser micromanipulation of microorganisms, DNA and virus , 2006, 2006 IEEE International Symposium on MicroNanoMechanical and Human Science.

[20]  Z. Lv,et al.  Protection of mice from lethal endotoxemia by chimeric human BPI-Fcgamma1 gene delivery. , 2006, Cellular & molecular immunology.

[21]  David J. Stevens,et al.  Haemagglutinin mutations responsible for the binding of H5N1 influenza A viruses to human-type receptors , 2006, Nature.

[22]  A. Ishihama,et al.  Host factor Ebp1: Selective inhibitor of influenza virus transcriptase , 2007, Genes to cells : devoted to molecular & cellular mechanisms.

[23]  Yong Qiang Gu,et al.  Application of optical tweezers in the research of molecular interaction between lymphocyte function associated antigen-1 and its monoclonal antibody. , 2007, Cellular & molecular immunology.

[24]  H. Klenk,et al.  Avian-virus-like receptor specificity of the hemagglutinin impedes influenza virus replication in cultures of human airway epithelium. , 2007, Virology.

[25]  Y. Kawaoka,et al.  The quail and chicken intestine have sialyl-galactose sugar chains responsible for the binding of influenza A viruses to human type receptors. , 2007, Glycobiology.

[26]  Thomas Aabo,et al.  Efficient optical trapping and visualization of silver nanoparticles. , 2008, Nano letters.

[27]  A. Honda Role of host protein Ebp1 in influenza virus growth: intracellular localization of Ebp1 in virus-infected and uninfected cells. , 2008, Journal of biotechnology.

[28]  Kotaro Minato,et al.  Cell Palpation System Based on a Force Measurement by Optical Tweezers for Investigation of Local Mechanical Properties of a Cell Membrane , 2009 .

[29]  S. Whelan,et al.  Vesicular Stomatitis Virus Enters Cells through Vesicles Incompletely Coated with Clathrin That Depend upon Actin for Internalization , 2009, PLoS pathogens.

[30]  Ari Helenius,et al.  Virus entry by endocytosis. , 2010, Annual review of biochemistry.

[31]  Ke Xu,et al.  Influenza A Virus Replication Induces Cell Cycle Arrest in G0/G1 Phase , 2010, Journal of Virology.

[32]  G. Melikyan,et al.  Driving a wedge between viral lipids blocks infection , 2010, Proceedings of the National Academy of Sciences.

[33]  H. Ewers,et al.  Analysis of virus entry and cellular membrane dynamics by single particle tracking. , 2012, Methods in enzymology.

[34]  Helmut Grubmüller,et al.  Influenza virus binds its host cell using multiple dynamic interactions , 2012, Proceedings of the National Academy of Sciences.