The Rab11 Pathway Is Required for Influenza A Virus Budding and Filament Formation

ABSTRACT Influenza A virus buds through the apical plasma membrane, forming enveloped virus particles that can take the shape of pleomorphic spheres or vastly elongated filaments. For either type of virion, the factors responsible for separation of viral and cell membranes are not known. We find that cellular Rab11 (a small GTP-binding protein involved in endocytic recycling) and Rab11-family interacting protein 3 ([FIP3] which plays a role in membrane trafficking and regulation of actin dynamics) are both required to support the formation of filamentous virions, while Rab11 is additionally involved in the final budding step of spherical particles. Cells transfected with Rab11 GTP-cycling mutants or depleted of Rab11 or FIP3 content by small interfering RNA treatment lost the ability to form virus filaments. Depletion of Rab11 resulted in up to a 100-fold decrease in titer of spherical virus released from cells. Scanning electron microscopy of Rab11-depleted cells showed high densities of virus particles apparently stalled in the process of budding. Transmission electron microscopy of thin sections confirmed that Rab11 depletion resulted in significant numbers of abnormally formed virus particles that had failed to pinch off from the plasma membrane. Based on these findings, we see a clear role for a Rab11-mediated pathway in influenza virus morphogenesis and budding.

[1]  W. Barclay,et al.  The M1 matrix protein controls the filamentous phenotype of influenza A virus. , 2004, Virology.

[2]  A. García-Sastre,et al.  Reverse genetics studies on the filamentous morphology of influenza A virus. , 2003, The Journal of general virology.

[3]  R. Scheller,et al.  Molecular Characterization of Rab11 Interactions with Members of the Family of Rab11-interacting Proteins* , 2004, Journal of Biological Chemistry.

[4]  J. Crowe,et al.  Apical recycling systems regulate directional budding of respiratory syncytial virus from polarized epithelial cells , 2003, Proceedings of the National Academy of Sciences of the United States of America.

[5]  G. Apodaca,et al.  Differential involvement of endocytic compartments in the biosynthetic traffic of apical proteins , 2007, The EMBO journal.

[6]  R. Lamb,et al.  Influenza Virus Hemagglutinin and Neuraminidase, but Not the Matrix Protein, Are Required for Assembly and Budding of Plasmid-Derived Virus-Like Particles , 2007, Journal of Virology.

[7]  Glenn C. Simon,et al.  Mechanisms regulating targeting of recycling endosomes to the cleavage furrow during cytokinesis. , 2008, Biochemical Society transactions.

[8]  W. Sullivan,et al.  Actin cytoskeleton remodeling during early Drosophila furrow formation requires recycling endosomal components Nuclear-fallout and Rab11 , 2003, The Journal of cell biology.

[9]  E. Medcalf,et al.  Identification of the domains of the influenza A virus M1 matrix protein required for NP binding, oligomerization and incorporation into virions , 2007, The Journal of general virology.

[10]  C. Browning,et al.  Phenanthridine Compounds as Chemotherapeutic Agents in Experimental T. cruzi Infections , 1946, Nature.

[11]  D. Pérez-Caballero,et al.  Divergent retroviral late-budding domains recruit vacuolar protein sorting factors by using alternative adaptor proteins , 2003, Proceedings of the National Academy of Sciences of the United States of America.

[12]  J. Galarza,et al.  Formation of Wild-Type and Chimeric Influenza Virus-Like Particles following Simultaneous Expression of Only Four Structural Proteins , 2001, Journal of Virology.

[13]  D. Ellis,et al.  A functional link between the actin cytoskeleton and lipid rafts during budding of filamentous influenza virions. , 2002, Virology.

[14]  A. Pekosz,et al.  Roles for the recycling endosome, Rab8, and Rab11 in hantavirus release from epithelial cells , 2008, Virology.

[15]  P. Roberts,et al.  Host cell dependence of viral morphology. , 1998, Proceedings of the National Academy of Sciences of the United States of America.

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

[17]  J. Donaldson Multiple Roles for Arf6: Sorting, Structuring, and Signaling at the Plasma Membrane* , 2003, Journal of Biological Chemistry.

[18]  Wesley I. Sundquist,et al.  Tsg101 and the Vacuolar Protein Sorting Pathway Are Essential for HIV-1 Budding , 2001, Cell.

[19]  C. Crump,et al.  Herpes Simplex Virus Type 1 Cytoplasmic Envelopment Requires Functional Vps4 , 2007, Journal of Virology.

[20]  Chadwick M. Hales,et al.  Rab11 Family Interacting Protein 2 Associates with Myosin Vb and Regulates Plasma Membrane Recycling* , 2002, The Journal of Biological Chemistry.

[21]  R. Wyckoff,et al.  Electron Micrography of the Virus of Influenza , 1946, Nature.

[22]  M. Zerial,et al.  Rab11 regulates recycling through the pericentriolar recycling endosome , 1996, The Journal of cell biology.

[23]  Wei Chen,et al.  Rab11 is required for trans-golgi network-to-plasma membrane transport and a preferential target for GDP dissociation inhibitor. , 1998, Molecular biology of the cell.

[24]  R. Lamb,et al.  The M1 and M2 proteins of influenza A virus are important determinants in filamentous particle formation. , 1998, Virology.

[25]  Peter Novick,et al.  Rabs and their effectors: Achieving specificity in membrane traffic , 2006, Proceedings of the National Academy of Sciences.

[26]  S. Inglis,et al.  Complex formation between influenza virus polymerase proteins expressed in Xenopus oocytes , 1989, Virology.

[27]  C. Horgan,et al.  Purification and functional properties of Rab11-FIP3. , 2005, Methods in enzymology.

[28]  P. Gómez-Puertas,et al.  Influenza Virus Matrix Protein Is the Major Driving Force in Virus Budding , 2000, Journal of Virology.

[29]  Marino Zerial,et al.  Rab proteins as membrane organizers , 2001, Nature Reviews Molecular Cell Biology.

[30]  O. Weisz,et al.  Apical trafficking in epithelial cells: signals, clusters and motors , 2009, Journal of Cell Science.

[31]  Z. Zhou,et al.  Influenza virus morphogenesis and budding , 2009, Virus Research.

[32]  Glenn C. Simon,et al.  The FIP3-Rab11 protein complex regulates recycling endosome targeting to the cleavage furrow during late cytokinesis. , 2004, Molecular biology of the cell.

[33]  Nicole A. Ducharme,et al.  Respiratory syncytial virus uses a Vps4-independent budding mechanism controlled by Rab11-FIP2 , 2008, Proceedings of the National Academy of Sciences.

[34]  Chadwick M. Hales,et al.  Identification and Characterization of a Family of Rab11-interacting Proteins* , 2001, The Journal of Biological Chemistry.

[35]  C. Horgan,et al.  The dynamic Rab11-FIPs. , 2009, Biochemical Society transactions.

[36]  G. Stuart,et al.  Direct measurement of specific membrane capacitance in neurons. , 2000, Biophysical journal.

[37]  S. Ferguson,et al.  Regulation of Angiotensin II Type 1A Receptor Intracellular Retention, Degradation, and Recycling by Rab5, Rab7, and Rab11 GTPases* , 2004, Journal of Biological Chemistry.

[38]  G. Spudich,et al.  Optineurin links myosin VI to the Golgi complex and is involved in Golgi organization and exocytosis , 2005, The Journal of cell biology.

[39]  H. Kräusslich,et al.  More than one door – Budding of enveloped viruses through cellular membranes , 2007, FEBS Letters.

[40]  Wendy S. Barclay,et al.  A Complicated Message: Identification of a Novel PB1-Related Protein Translated from Influenza A Virus Segment 2 mRNA , 2009, Journal of Virology.

[41]  O. Krizanova,et al.  Changes in ultrastructure and endogenous ionic channels activity during culture of HEK 293 cell line. , 2007, European journal of pharmacology.

[42]  E. D. Kilbourne,et al.  Genetic studies of influenza viruses. I. Viral morphology and growth capacity as exchangeable genetic traits. Rapid in ovo adaptation of early passage Asian strain isolates by combination with PR8. , 1960 .

[43]  M. Zerial,et al.  Rab11, a small GTPase associated with both constitutive and regulated secretory pathways in PC12 cells , 1993, FEBS letters.

[44]  D. Robinson,et al.  Two GTPase isoforms, Ypt31p and Ypt32p, are essential for Golgi function in yeast. , 1996, The EMBO journal.

[45]  M. Amorim,et al.  Nuclear Export of Influenza A Virus mRNAs Requires Ongoing RNA Polymerase II Activity , 2007, Traffic.

[46]  H. Klenk,et al.  New low-viscosity overlay medium for viral plaque assays , 2006, Virology Journal.

[47]  W. Britt,et al.  HCMV‐Encoded Glycoprotein M (UL100) Interacts with Rab11 Effector Protein FIP4 , 2009, Traffic.

[48]  W. Sundquist,et al.  The Protein Network of HIV Budding , 2003, Cell.

[49]  P. Digard,et al.  Budding of filamentous and non-filamentous influenza A virus occurs via a VPS4 and VPS28-independent pathway. , 2009, Virology.

[50]  P. Bieniasz,et al.  HIV-1 and Ebola virus encode small peptide motifs that recruit Tsg101 to sites of particle assembly to facilitate egress , 2001, Nature Medicine.

[51]  Alexander V. Zhdanov,et al.  Rab11‐FIP3 Is Critical for the Structural Integrity of the Endosomal Recycling Compartment , 2007, Traffic.

[52]  M. Amorim,et al.  Lipid Raft‐Dependent Targeting of the Influenza A Virus Nucleoprotein to the Apical Plasma Membrane , 2004, Traffic.

[53]  R. Lamb,et al.  Mechanisms for enveloped virus budding: can some viruses do without an ESCRT? , 2008, Virology.

[54]  A. Osterhaus,et al.  Efficient generation and growth of influenza virus A/PR/8/34 from eight cDNA fragments. , 2004, Virus research.

[55]  J. Gog,et al.  Mutational Analysis of cis-Acting RNA Signals in Segment 7 of Influenza A Virus , 2008, Journal of Virology.

[56]  P. H. Anborgh,et al.  beta 2-adrenergic receptor internalization, endosomal sorting, and plasma membrane recycling are regulated by rab GTPases. , 2000, The Journal of biological chemistry.

[57]  R. Compans,et al.  An electron microscopic study of single-cycle infection of chick embryo fibroblasts by influenza virus. , 1969, Virology.

[58]  R. Prekeris,et al.  Rab11-FIP3 is a Rab11-binding protein that regulates breast cancer cell motility by modulating the actin cytoskeleton. , 2009, European journal of cell biology.