This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Sandoval, I. V.
Right arrow Articles by Carrasco, L.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Sandoval, I. V.
Right arrow Articles by Carrasco, L.

 Previous Article  |  Next Article 

J. Virol., 06 1997, 4679-4693, Vol 71, No. 6
Copyright © 1997, American Society for Microbiology

Poliovirus infection and expression of the poliovirus protein 2B provoke the disassembly of the Golgi complex, the organelle target for the antipoliovirus drug Ro-090179

IV Sandoval and L Carrasco
Centro de Biologia Molecular, Facultad de Ciencias, Universidad Autonoma de Madrid, Cantoblanco, Spain.

Infection of Vero cells with poliovirus results in complete disassembly of the Golgi complex. Milestones of the process of disassembly are the release to the cytosol of the beta-COP bound to Golgi membranes, the disruption of the cis-Golgi network into fragments scattered throughout the cytoplasm, and the disassembly of the stacked cisternae by a process mediated by long tubular structures. Transient expression of the viral protein 2B in COS-7 cells also causes the disassembly of the Golgi complex by a process preceded by the accumulation of the protein in the Golgi area. Vero cells infected for 3 h show no recognizable Golgi complexes at the ultrastructural level and display an enormously swollen endoplasmic reticulum (ER) with extensive areas of its surface heavily coated. Ro-090179 (Ro), a flavonoid isolated from the herb Agastache rugosa, provokes the specific swelling and disruption of the Golgi complex and strongly inhibits poliovirus infection. Ro provokes the swelling and the disruption of the stacked cisternae and trans- Golgi elements without affecting the cis-most Golgi cisternae much. Moreover, Ro inhibits the fusion of the Golgi complex with the ER in cells treated with brefeldin A and provokes the accumulation of the intermediate compartment membrane protein p58 into ERD2-positive Golgi elements but has no effect on the anterograde transport involved in protein secretion. Our results indicate that the secretory pathway and specifically the Golgi complex are preferential targets of poliovirus.


This article has been cited by other articles:

  • Oh, H. S., Pathak, H. B., Goodfellow, I. G., Arnold, J. J., Cameron, C. E. (2009). Insight into Poliovirus Genome Replication and Encapsidation Obtained from Studies of 3B-3C Cleavage Site Mutants. J. Virol. 83: 9370-9387 [Abstract] [Full Text]  
  • Piccone, M. E., Feng, Y., Chang, A. C. Y., Mosseri, R., Lu, Q., Kutish, G. F., Lu, Z., Burrage, T. G., Gooch, C., Rock, D. L., Cohen, S. N. (2009). Identification of Cellular Genes Affecting the Infectivity of Foot-and-Mouth Disease Virus. J. Virol. 83: 6681-6688 [Abstract] [Full Text]  
  • Armer, H., Moffat, K., Wileman, T., Belsham, G. J., Jackson, T., Duprex, W. P., Ryan, M., Monaghan, P. (2008). Foot-and-Mouth Disease Virus, but Not Bovine Enterovirus, Targets the Host Cell Cytoskeleton via the Nonstructural Protein 3Cpro. J. Virol. 82: 10556-10566 [Abstract] [Full Text]  
  • de Jong, A. S., de Mattia, F., Van Dommelen, M. M., Lanke, K., Melchers, W. J. G., Willems, P. H. G. M., van Kuppeveld, F. J. M. (2008). Functional Analysis of Picornavirus 2B Proteins: Effects on Calcium Homeostasis and Intracellular Protein Trafficking. J. Virol. 82: 3782-3790 [Abstract] [Full Text]  
  • Beske, O., Reichelt, M., Taylor, M. P., Kirkegaard, K., Andino, R. (2007). Poliovirus infection blocks ERGIC-to-Golgi trafficking and induces microtubule-dependent disruption of the Golgi complex. J. Cell Sci. 120: 3207-3218 [Abstract] [Full Text]  
  • Yin, J., Liu, Y., Wimmer, E., Paul, A. V. (2007). Complete protein linkage map between the P2 and P3 non-structural proteins of poliovirus. J. Gen. Virol. 88: 2259-2267 [Abstract] [Full Text]  
  • de Jong, A. S., Visch, H.-J., de Mattia, F., van Dommelen, M. M., Swarts, H. G., Luyten, T., Callewaert, G., Melchers, W. J., Willems, P. H., van Kuppeveld, F. J. (2006). The Coxsackievirus 2B Protein Increases Efflux of Ions from the Endoplasmic Reticulum and Golgi, thereby Inhibiting Protein Trafficking through the Golgi. J. Biol. Chem. 281: 14144-14150 [Abstract] [Full Text]  
  • Belov, G. A., Fogg, M. H., Ehrenfeld, E. (2005). Poliovirus Proteins Induce Membrane Association of GTPase ADP-Ribosylation Factor. J. Virol. 79: 7207-7216 [Abstract] [Full Text]  
  • Harris, J. R., Racaniello, V. R. (2005). Amino Acid Changes in Proteins 2B and 3A Mediate Rhinovirus Type 39 Growth in Mouse Cells. J. Virol. 79: 5363-5373 [Abstract] [Full Text]  
  • Knox, C., Moffat, K., Ali, S., Ryan, M., Wileman, T. (2005). Foot-and-mouth disease virus replication sites form next to the nucleus and close to the Golgi apparatus, but exclude marker proteins associated with host membrane compartments. J. Gen. Virol. 86: 687-696 [Abstract] [Full Text]  
  • de Jong, A. S., Melchers, W. J. G., Glaudemans, D. H. R. F., Willems, P. H. G. M., van Kuppeveld, F. J. M. (2004). Mutational Analysis of Different Regions in the Coxsackievirus 2B Protein: REQUIREMENTS FOR HOMO-MULTIMERIZATION, MEMBRANE PERMEABILIZATION, SUBCELLULAR LOCALIZATION, AND VIRUS REPLICATION. J. Biol. Chem. 279: 19924-19935 [Abstract] [Full Text]  
  • Fernandez-Vega, V., Sosnovtsev, S. V., Belliot, G., King, A. D., Mitra, T., Gorbalenya, A., Green, K. Y. (2004). Norwalk Virus N-Terminal Nonstructural Protein Is Associated with Disassembly of the Golgi Complex in Transfected Cells. J. Virol. 78: 4827-4837 [Abstract] [Full Text]  
  • Monaghan, P., Cook, H., Jackson, T., Ryan, M., Wileman, T. (2004). The ultrastructure of the developing replication site in foot-and-mouth disease virus-infected BHK-38 cells. J. Gen. Virol. 85: 933-946 [Abstract] [Full Text]  
  • Crotty, S., Saleh, M.-C., Gitlin, L., Beske, O., Andino, R. (2004). The Poliovirus Replication Machinery Can Escape Inhibition by an Antiviral Drug That Targets a Host Cell Protein. J. Virol. 78: 3378-3386 [Abstract] [Full Text]  
  • de Jong, A. S., Wessels, E., Dijkman, H. B. P. M., Galama, J. M. D., Melchers, W. J. G., Willems, P. H. G. M., van Kuppeveld, F. J. M. (2003). Determinants for Membrane Association and Permeabilization of the Coxsackievirus 2B Protein and the Identification of the Golgi Complex as the Target Organelle. J. Biol. Chem. 278: 1012-1021 [Abstract] [Full Text]  
  • Agirre, A., Barco, A., Carrasco, L., Nieva, J. L. (2002). Viroporin-mediated Membrane Permeabilization. PORE FORMATION BY NONSTRUCTURAL POLIOVIRUS 2B PROTEIN. J. Biol. Chem. 277: 40434-40441 [Abstract] [Full Text]  
  • van Kuppeveld, F. J. M., Melchers, W. J. G., Willems, P. H. G. M., Gadella, T. W. J. Jr. (2002). Homomultimerization of the Coxsackievirus 2B Protein in Living Cells Visualized by Fluorescence Resonance Energy Transfer Microscopy. J. Virol. 76: 9446-9456 [Abstract] [Full Text]  
  • Sosnovtsev, S. V., Garfield, M., Green, K. Y. (2002). Processing Map and Essential Cleavage Sites of the Nonstructural Polyprotein Encoded by ORF1 of the Feline Calicivirus Genome. J. Virol. 76: 7060-7072 [Abstract] [Full Text]  
  • de Jong, A. S., Schrama, I. W. J., Willems, P. H. G. M., Galama, J. M. D., Melchers, W. J. G., van Kuppeveld, F. J. M. (2002). Multimerization reactions of coxsackievirus proteins 2B, 2C and 2BC: a mammalian two-hybrid analysis. J. Gen. Virol. 83: 783-793 [Abstract] [Full Text]  
  • van Kuppeveld, F. J. M., van den Hurk, P. J. J. C., Schrama, I. W. J., Galama, J. M. D., Melchers, W. J. G. (2002). Trans-complementation of a genetic defect in the coxsackie B3 virus 2B protein. J. Gen. Virol. 83: 341-350 [Abstract] [Full Text]  
  • Neznanov, N., Kondratova, A., Chumakov, K. M., Angres, B., Zhumabayeva, B., Agol, V. I., Gudkov, A. V. (2001). Poliovirus Protein 3A Inhibits Tumor Necrosis Factor (TNF)-Induced Apoptosis by Eliminating the TNF Receptor from the Cell Surface. J. Virol. 75: 10409-10420 [Abstract] [Full Text]  
  • Rust, R. C., Landmann, L., Gosert, R., Tang, B. L., Hong, W., Hauri, H.-P., Egger, D., Bienz, K. (2001). Cellular COPII Proteins Are Involved in Production of the Vesicles That Form the Poliovirus Replication Complex. J. Virol. 75: 9808-9818 [Abstract] [Full Text]  
  • Teterina, N. L., Egger, D., Bienz, K., Brown, D. M., Semler, B. L., Ehrenfeld, E. (2001). Requirements for Assembly of Poliovirus Replication Complexes and Negative-Strand RNA Synthesis. J. Virol. 75: 3841-3850 [Abstract] [Full Text]  
  • Suhy, D. A., Giddings, T. H. Jr., Kirkegaard, K. (2000). Remodeling the Endoplasmic Reticulum by Poliovirus Infection and by Individual Viral Proteins: an Autophagy-Like Origin for Virus-Induced Vesicles. J. Virol. 74: 8953-8965 [Abstract] [Full Text]  
  • Carette, J. E., Stuiver, M., Van Lent, J., Wellink, J., Van Kammen, A. (2000). Cowpea Mosaic Virus Infection Induces a Massive Proliferation of Endoplasmic Reticulum but Not Golgi Membranes and Is Dependent on De Novo Membrane Synthesis. J. Virol. 74: 6556-6563 [Abstract] [Full Text]  
  • Egger, D., Teterina, N., Ehrenfeld, E., Bienz, K. (2000). Formation of the Poliovirus Replication Complex Requires Coupled Viral Translation, Vesicle Production, and Viral RNA Synthesis. J. Virol. 74: 6570-6580 [Abstract] [Full Text]  
  • Rojo, M, Emery, G, Marjomaki, V, McDowall, A., Parton, R., Gruenberg, J (2000). The transmembrane protein p23 contributes to the organization of the Golgi apparatus. J. Cell Sci. 113: 1043-1057 [Abstract]  
  • Hauri, H., Kappeler, F, Andersson, H, Appenzeller, C (2000). ERGIC-53 and traffic in the secretory pathway. J. Cell Sci. 113: 587-596 [Abstract]  
  • del Valle, M, Robledo, Y, Sandoval, I. (1999). Membrane flow through the Golgi apparatus: specific disassembly of the cis-Golgi network by ATP depletion. J. Cell Sci. 112: 4017-4029 [Abstract]  
  • Bolten, R., Egger, D., Gosert, R., Schaub, G., Landmann, L., Bienz, K. (1998). Intracellular Localization of Poliovirus Plus- and Minus-Strand RNA Visualized by Strand-Specific Fluorescent In Situ Hybridization. J. Virol. 72: 8578-8585 [Abstract] [Full Text]  
  • Cuconati, A., Molla, A., Wimmer, E. (1998). Brefeldin A Inhibits Cell-Free, De Novo Synthesis of Poliovirus. J. Virol. 72: 6456-6464 [Abstract] [Full Text]  
  • Barco, A., Carrasco, L. (1998). Identification of Regions of Poliovirus 2BC Protein That Are Involved in Cytotoxicity. J. Virol. 72: 3560-3570 [Abstract] [Full Text]  
  • Cuconati, A., Xiang, W., Lahser, F., Pfister, T., Wimmer, E. (1998). A Protein Linkage Map of the P2 Nonstructural Proteins of Poliovirus. J. Virol. 72: 1297-1307 [Abstract] [Full Text]