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


     


J Gen Virol 35 (1977), 361-368; DOI 10.1099/0022-1317-35-2-361
© 1977 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 CrossRef
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Rasmussen, L.
Right arrow Articles by Merigan, T. C.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Rasmussen, L.
Right arrow Articles by Merigan, T. C.
Agricola
Right arrow Articles by Rasmussen, L.
Right arrow Articles by Merigan, T. C.

Multiplicity-dependent Replication of Varicella-zoster Virus in Interferon-treated Cells

Lucy Rasmussen, Ann R. Holmes, Barbara Hofmeister and Thomas C. Merigan

Division of Infectious Diseases, Department of Medicine, Stanford University School of Medicine, Stanford, California, 94305, U.S.A.

The inhibitory effects of interferon (IF) on the replication of varicella-zoster (VZ) virus in human foreskin fibroblast (HFF) cultures inoculated with infected cells or with cell-free virus were assayed by measuring (1) yields of infected cells, (2) plaques, (3) microfoci and (4) cytopathic effects. More If was needed to reduce yields of infected cells at high input multiplicities of challenge than at low input multiplicities, and still more IF was needed to prevent cytopathology due to VZ virus. A cell-free virus inoculum was more sensitive to the inhibitory effects of IF than an inoculum of infected cells. With the latter, but not with cell-free virus, the continuous presence of IF in the medium was necessary for it to express its maximum antiviral activity. To explain these results, it is suggested that some herpesviruses may establish ‘reservoirs’ of infectivity and thus provide a prolonged challenge to IF-treated cells which are not uniformly resistant to infection.

Received 21 September 1976; accepted 31 December 1976.





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 © 1977 by the Society for General Microbiology.