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


     


J Gen Virol 78 (1997), 563-566
© 1997 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 Tobita, K.
Right arrow Articles by Hayase, Y.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Tobita, K.
Right arrow Articles by Hayase, Y.
Agricola
Right arrow Articles by Tobita, K.
Right arrow Articles by Hayase, Y.

Journal of General Virology, Vol 78, 563-566, Copyright © 1997 by Society for General Microbiology


ARTICLES

Spontaneous excretion of virus from MDCK cells persistently infected with influenza virus A/PR/8/34

K Tobita, T Tanaka and Y Hayase
Department of Virology, Jichi Medical School, Minami-Kawachi-Machi, Tochigi-Ken, Japan. tobikiyo@jichi.ac.jp

When MDCK cells in a semiconfluent monolayer were infected with 5 p.f.u. per cell of influenza virus A/PR/8/34 (H1N1), a majority of the cells continued to grow stably upon subsequent cultivation with a growth medium containing 50% foetal calf serum. While growing, the cells spontaneously excreted virus, the amount of which declined gradually as the passage number of the cells increased. The extent of virus shedding was significantly increased when the cells were subsequently maintained in a medium containing 0.2% bovine serum albumin. Within the cells, viral messenger RNAs for all eight genes of A/PR/8 were demonstrated by PCR indicating that endogenous viral genes were constitutively transcribed. However, viral proteins as well as viral genes were not demonstrable by radioimmunoprecipitation or ribonuclease protection assays, respectively.


This article has been cited by other articles:


Home page
J. Virol.Home page
M. Krasnitz, A. J. Levine, and R. Rabadan
Anomalies in the Influenza Virus Genome Database: New Biology or Laboratory Errors?
J. Virol., September 1, 2008; 82(17): 8947 - 8950.
[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 © 1997 by the Society for General Microbiology.