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


     


J Gen Virol 73 (1992), 1739-1744; DOI 10.1099/0022-1317-73-7-1739
© 1992 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 Kronenberger, P.
Right arrow Articles by Boeyé, A.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Kronenberger, P.
Right arrow Articles by Boeyé, A.
Agricola
Right arrow Articles by Kronenberger, P.
Right arrow Articles by Boeyé, A.

Compartmentalization of subviral particles during poliovirus eclipse in HeLa cells

Peter Kronenberger, Raf Vrijsen and Albert Boeyé

Department of Microbiology and Hygiene, Vrije Universiteit Brussel, Laarbeeklaan 103, B-1090 Brussels, Belgium

HeLa cells were preincubated with radiolabelled poliovirus type 1 at 26 °C, such that the 160S virions were internalized, but not altered structurally. The temperature was then shifted to 37 °C to study the intracellular redistribution of the virions and the modifications they undergo at that temperature. Using subcellular fractionation in isoosmotic Nycodenz gradients, we obtained evidence for the rapid loss of virions from the plasma membrane and from a vesicular fraction, as well as for the formation of two populations of intracellular 135S particles. The first population was associated with lysosomes and was slowly converted to (RNA-containing) 110S particles. In the presence of the lysosomotropic agent chloroquine, the lysosomal 135S population was converted to 80S empty capsids. The second 135S population, which was not associated with any organelle, was converted to 80S empty capsids. Similar observations were made during unsynchronized infection at 37 °C. We propose a model for infection in which 135S particles cross a membrane barrier, and are uncoated in the cytosol.

Received 30 January 1991; accepted 17 March 1992.


This article has been cited by other articles:


Home page
J. Virol.Home page
V. Marjomaki, V. Pietiainen, H. Matilainen, P. Upla, J. Ivaska, L. Nissinen, H. Reunanen, P. Huttunen, T. Hyypia, and J. Heino
Internalization of Echovirus 1 in Caveolae
J. Virol., February 15, 2002; 76(4): 1856 - 1865.
[Abstract] [Full Text] [PDF]


Home page
J. Virol.Home page
D. Schober, P. Kronenberger, E. Prchla, D. Blaas, and R. Fuchs
Major and Minor Receptor Group Human Rhinoviruses Penetrate from Endosomes by Different Mechanisms
J. Virol., February 1, 1998; 72(2): 1354 - 1364.
[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 © 1992 by the Society for General Microbiology.