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


     


J Gen Virol 65 (1984), 2269-2272; DOI 10.1099/0022-1317-65-12-2269
© 1984 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 Landini, M. P.
Right arrow Articles by Rugolo, M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Landini, M. P.
Right arrow Articles by Rugolo, M.
Agricola
Right arrow Articles by Landini, M. P.
Right arrow Articles by Rugolo, M.

Increased Accumulation of a Lipophilic Cation (Tetraphenylphosphonium) in Human Embryo Fibroblasts after Infection with Cytomegalovirus

M. P. Landini and M. Rugolo1

Institute of Microbiology, Medical School, St Orsola General Hospital, Via Massarenti, 9, 40138 Bologna
and1 Institute of Botany, University of Bologna, Bologna, Italy

The distribution of a lipophilic cation, tetraphenylphosphonium (TPP+), has been used to monitor changes in mitochondrial and plasma membrane potentials within human embryo fibroblasts infected with human cytomegalovirus. An increase in TPP+ accumulation was observed throughout the whole viral replication cycle, beginning 6 h after infection. This effect requires an active viral DNA and seems to be dependent on the early transcription of the viral genome. In the early phase of viral replication, the increase in TPP+ accumulation is insensitive to mitochondrial inhibitors and sensitive to ouabain, and could be due to a hyperpolarization of the plasma membrane. Later during the infectious cycle, enhanced accumulation of the lipophilic cation is sensitive to mitochondrial inhibitors.

Keywords: HCMV, early, transcription, membrane potentials, lipophilic cation

Received 29 May 1984; accepted 3 August 1984.


This article has been cited by other articles:


Home page
J. Virol.Home page
A. L. McCormick, V. L. Smith, D. Chow, and E. S. Mocarski
Disruption of Mitochondrial Networks by the Human Cytomegalovirus UL37 Gene Product Viral Mitochondrion-Localized Inhibitor of Apoptosis
J. Virol., December 6, 2002; 77(1): 631 - 641.
[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 © 1984 by the Society for General Microbiology.