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


     


J Gen Virol 72 (1991), 1871-1876; DOI 10.1099/0022-1317-72-8-1871
© 1991 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 Aboagye-Mathiesen, G.
Right arrow Articles by Ebbesen, P.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Aboagye-Mathiesen, G.
Right arrow Articles by Ebbesen, P.
Agricola
Right arrow Articles by Aboagye-Mathiesen, G.
Right arrow Articles by Ebbesen, P.

Characterization Of Sendai Virus-Induced Human Placental Trophoblast Interferons

George Aboagye-Mathiesen1, Ferenc D. Tóth1,2,, Claus Juhl1, Niels Nørskov-Lauritsen1, Peter M. Petersen1, Vladimir Zachar1,3, and Peter Ebbesen1

The1 Danish Cancer Society, Department of Virus and Cancer, Gustav Wieds Vej 10, DK-8000 Aarhus C, Denmark
2 Institute of Microbiology, Medical University, H-4012 Debrecen, Hungary
and3 Institute of Virology, Slovak Academy of Sciences, Bratislava, Czechoslovakia

Human placental trophoblast cultures produce a mixture of interferons (IFNs) when challenged with Sendai virus. High-performance dye-ligand and immunoaffinity chromatography of a trophoblast IFN (tro-IFN) preparation enabled the isolation of three antigenically distinct IFNs, {alpha}I, {alpha}II1 and beta, with Mrs of 16K, 22K and 24K respectively, by reducing and non-reducing SDS-PAGE. The major IFN, responsible for 75% of the total antiviral activity, was tro-IFN-beta, with the remaining activity being due to tro-IFN-{alpha}I and tro-IFN-{alpha}II1, as determined by an antiviral neutralization test using specific anti-human IFN antibodies. The antiviral activities of the tro-IFNs were stable at pH 2·0 for 24 h and tro-IFN-{alpha}II1 and -beta were shown to be glycoproteins. The three tro-IFNs showed different antiviral activities when assayed on human and bovine cell species; tro-IFN-{alpha}I and -{alpha}II1 protected both human and bovine (MDBK) cells from virus infection, whereas tro-IFN-beta showed a high degree of species specificity, protecting only the human cell types tested.

Received 7 December 1990; accepted 2 April 1991.





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 © 1991 by the Society for General Microbiology.