This Article
Right arrow Full Text
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 Arita, M.
Right arrow Articles by Nomoto, A.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Arita, M.
Right arrow Articles by Nomoto, A.

 Previous Article  |  Next Article 

Journal of Virology, February 1999, p. 1066-1074, Vol. 73, No. 2
0022-538X/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.

Interaction of Poliovirus with Its Receptor Affords a High Level of Infectivity to the Virion in Poliovirus Infections Mediated by the Fc Receptor

Minetaro Arita,1 Hitoshi Horie,2 Mineo Arita,3 and Akio Nomoto1,*

Department of Microbiology, The Institute of Medical Science, The University of Tokyo, Minato-ku, Tokyo 108-8639,1 Japan Poliomyelitis Research Institute, Higashimurayama, Tokyo 189-0003,2 and Department of Viral Disease and Vaccine Control, National Institute of Health, Musashimurayama, Tokyo 208-0011,3 Japan

Received 17 August 1998/Accepted 21 October 1998

Poliovirus infects susceptible cells through the poliovirus receptor (PVR), which functions to bind virus and to change its conformation. These two activities are thought to be necessary for efficient poliovirus infection. How binding and conformation conversion activities contribute to the establishment of poliovirus infection was investigated. Mouse L cells expressing mouse high-affinity Fcgamma receptor molecules were established and used to study poliovirus infection mediated by mouse antipoliovirus monoclonal antibodies (MAbs) (immunoglobulin G2a [IgG2a] subtypes) or PVR-IgG2a, a chimeric molecule consisting of the extracellular moiety of PVR and the hinge and Fc portion of mouse IgG2a. The antibodies and PVR-IgG2a showed the same degree of affinity for poliovirus, but the infectivities mediated by these molecules were different. Among the molecules tested, PVR-IgG2a mediated the infection most efficiently, showing 50- to 100-fold-higher efficiency than that attained with the different MAbs. A conformational change of poliovirus was induced only by PVR-IgG2a. These results strongly suggested that some specific interaction(s) between poliovirus and the PVR is required for high-level infectivity of poliovirus in this system.


* Corresponding author. Mailing address: Department of Microbiology, The Institute of Medical Science, The University of Tokyo, 4-6-1 Shiroganedai, Minato-ku, Tokyo 108-8639, Japan. Phone: 81-3-5449-5501. Fax: 81-3-5449-5408. E-mail: anomoto{at}ims.u-tokyo.ac.jp.


Journal of Virology, February 1999, p. 1066-1074, Vol. 73, No. 2
0022-538X/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.



This article has been cited by other articles:

  • Arita, M., Ami, Y., Wakita, T., Shimizu, H. (2008). Cooperative Effect of the Attenuation Determinants Derived from Poliovirus Sabin 1 Strain Is Essential for Attenuation of Enterovirus 71 in the NOD/SCID Mouse Infection Model. J. Virol. 82: 1787-1797 [Abstract] [Full Text]  
  • Arita, M., Nagata, N., Iwata, N., Ami, Y., Suzaki, Y., Mizuta, K., Iwasaki, T., Sata, T., Wakita, T., Shimizu, H. (2007). An Attenuated Strain of Enterovirus 71 Belonging to Genotype A Showed a Broad Spectrum of Antigenicity with Attenuated Neurovirulence in Cynomolgus Monkeys. J. Virol. 81: 9386-9395 [Abstract] [Full Text]  
  • Arita, M., Nagata, N., Sata, T., Miyamura, T., Shimizu, H. (2006). Quantitative analysis of poliomyelitis-like paralysis in mice induced by a poliovirus replicon.. J. Gen. Virol. 87: 3317-3327 [Abstract] [Full Text]  
  • Baravalle, G., Brabec, M., Snyers, L., Blaas, D., Fuchs, R. (2004). Human Rhinovirus Type 2-Antibody Complexes Enter and Infect Cells via Fc-{gamma} Receptor IIB1. J. Virol. 78: 2729-2737 [Abstract] [Full Text]  
  • Mueller, S., Wimmer, E. (2003). Recruitment of Nectin-3 to Cell-Cell Junctions through trans-Heterophilic Interaction with CD155, a Vitronectin and Poliovirus Receptor That Localizes to {alpha}v{beta}3 Integrin-containing Membrane Microdomains. J. Biol. Chem. 278: 31251-31260 [Abstract] [Full Text]  
  • Silberstein, E., Dveksler, G., Kaplan, G. G. (2001). Neutralization of Hepatitis A Virus (HAV) by an Immunoadhesin Containing the Cysteine-Rich Region of HAV Cellular Receptor-1. J. Virol. 75: 717-725 [Abstract] [Full Text]  
  • Dotzauer, A., Gebhardt, U., Bieback, K., Göttke, U., Kracke, A., Mages, J., Lemon, S. M., Vallbracht, A. (2000). Hepatitis A Virus-Specific Immunoglobulin A Mediates Infection of Hepatocytes with Hepatitis A Virus via the Asialoglycoprotein Receptor. J. Virol. 74: 10950-10957 [Abstract] [Full Text]  
  • Huang, Y., Hogle, J. M., Chow, M. (2000). Is the 135S Poliovirus Particle an Intermediate during Cell Entry?. J. Virol. 74: 8757-8761 [Abstract] [Full Text]  
  • Belnap, D. M., Filman, D. J., Trus, B. L., Cheng, N., Booy, F. P., Conway, J. F., Curry, S., Hiremath, C. N., Tsang, S. K., Steven, A. C., Hogle, J. M. (2000). Molecular Tectonic Model of Virus Structural Transitions: the Putative Cell Entry States of Poliovirus. J. Virol. 74: 1342-1354 [Abstract] [Full Text]