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


     


J Gen Virol 25 (1974), 351-357; DOI 10.1099/0022-1317-25-3-351
© 1974 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 Appleyard, G.
Right arrow Articles by Maber, H. B.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Appleyard, G.
Right arrow Articles by Maber, H. B.
Agricola
Right arrow Articles by Appleyard, G.
Right arrow Articles by Maber, H. B.

Plaque Formation by Influenza Viruses in the Presence of Trypsin

G. Appleyard and H. B. Maber

Microbiological Research Establishment, Porton, Nr Salisbury, Wiltshire, U.K.

Eight strains of influenza virus were titrated as plaque-forming units in both monolayers and suspensions of chick embryo cells. In the absence of trypsin, satisfactory plaques were formed only by the A/WSN strain of virus. When trypsin was included in the overlay medium of cell monolayers, all the influenza virus strains tested produced plaques, and the plaque infectivities of all but one strain were close to the egg infectivities. Using cells suspended in agar in the presence of trypsin, four strains gave plaque infectivities indistinguishable from egg infectivities, two strains formed plaques with rather low efficiency and two strains did not produce plaques. Plaque formation was also enhanced by pronase or subtilisin. A preliminary investigation was made of the mode of action of trypsin.

Received 19 June 1974; accepted 12 August 1974.


This article has been cited by other articles:


Home page
J. Virol.Home page
J. M. Ngunjiri, M. J. Sekellick, and P. I. Marcus
Clonogenic Assay of Type A Influenza Viruses Reveals Noninfectious Cell-Killing (Apoptosis-Inducing) Particles
J. Virol., March 15, 2008; 82(6): 2673 - 2680.
[Abstract] [Full Text] [PDF]


Home page
Antimicrob. Agents Chemother.Home page
C. Sweet, K. J. Jakeman, K. Bush, P. C. Wagaman, L. A. Mckown, A. J. Streeter, D. Desai-Krieger, P. Chand, and Y. S. Babu
Oral Administration of Cyclopentane Neuraminidase Inhibitors Protects Ferrets against Influenza Virus Infection
Antimicrob. Agents Chemother., April 1, 2002; 46(4): 996 - 1004.
[Abstract] [Full Text] [PDF]


Home page
J. Virol.Home page
C. Scholtissek, J. Stech, S. Krauss, and R. G. Webster
Cooperation between the Hemagglutinin of Avian Viruses and the Matrix Protein of Human Influenza A Viruses
J. Virol., February 15, 2002; 76(4): 1781 - 1786.
[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 © 1974 by the Society for General Microbiology.