J Gen Virol
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


J Gen Virol 70 (1989), 2179-2184; DOI 10.1099/0022-1317-70-8-2179
© 1989 Society for General Microbiology

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 Email this article to a friend
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 arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via CrossRef
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Stannard, L. M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Stannard, L. M.
Agricola
Right arrow Articles by Stannard, L. M.

beta2 Microglobulin Binds to the Tegument of Cytomegalovirus: an Immunogold Study

Linda M. Stannard

Department of Medical Microbiology, University of Cape Town Medical School, Observatory Cape Town, South Africa, 7925

Previous reports have provided evidence for the ability of human cytomegalovirus (HCMV) to bind the host protein beta2 microglobulin (beta2m) from body fluids or culture medium, and thus enhance infectivity of the virus, both by evasion of immune neutralization and the capacity to employ the bound beta2m for attachment to the host cell. Immunocytochemical techniques and negative stain electron microscopy were used to identify the ultrastructural components of HCMV involved in its interaction with beta2m. Probes comprising colloidal gold coupled to beta2m were seen to bind not to the envelope as previously suspected, but to material closely surrounding the nucleocapsids. It is postulated that the tegument proteins of HCMV, via their capacity to bind beta2m, play an important role in the preservation of infectivity of disrupted virions by enabling unenveloped capsids to bind to cells and gain entry by a pathway other than that normally taken by intact virions.

Keywords: CMV, human, microglobulin, tegument

Received 12 December 1988; accepted 10 April 1989.


This article has been cited by other articles:


Home page
J. Virol.Home page
S. M. Varnum, D. N. Streblow, M. E. Monroe, P. Smith, K. J. Auberry, L. Pasa-Tolic, D. Wang, D. G. Camp II, K. Rodland, S. Wiley, et al.
Identification of Proteins in Human Cytomegalovirus (HCMV) Particles: the HCMV Proteome
J. Virol., October 15, 2004; 78(20): 10960 - 10966.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
INT J SYST EVOL MICROBIOL MICROBIOLOGY J GEN VIROL
J MED MICROBIOL ALL SGM JOURNALS
Copyright © 1989 by the Society for General Microbiology.