J Gen Virol Faster Access
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


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
Right arrow Citation Map
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 Schat, K. A.
Right arrow Articles by Koch, G.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Schat, K. A.
Right arrow Articles by Koch, G.
Agricola
Right arrow Articles by Schat, K. A.
Right arrow Articles by Koch, G.

Journal of General Virology, Vol 79, 841-849, Copyright © 1998 by Society for General Microbiology


ARTICLES

Open reading frame L1 of Marek's disease herpesvirus is not essential for in vitro and in vivo virus replication and establishment of latency

KA Schat, BJ Hooft van Iddekinge, H Boerrigter, PH O'Connell and G Koch
Department of Microbiology and Immunology, College of Veterinary Medicine, Cornell University, Ithaca, NY 14853, USA. kas24@Cornell.edu

Two mutant CV1988 Marek's disease virus (MDV) strains were developed in which a part of ORF L1 was replaced by lacZ with the SV40 early promoter. These mutant strains, CVIL1LacZ-A and -B, were inoculated into chickens to test the hypothesis that ORF L1 is involved in the induction and/or maintenance of latency. Mutant virus could be reisolated from lymphocytes obtained from chickens during both the lytic and latent phase of infection, indicating that ORF L1 is not essential for the induction and/or maintenance of latency or the reactivation from latency. Beta-galactosidase-positive lymphocytes were detected during the latent infection demonstrating that the SV40 early promoter can be active in recombinant MDV strains during latent infection. Although the insertion of lacZ was stable in cell culture, recombination within lacZ and the BamHI-L fragment was observed during in vivo infection.


This article has been cited by other articles:


Home page
J. Virol.Home page
Y. Yao, Y. Zhao, H. Xu, L. P. Smith, C. H. Lawrie, M. Watson, and V. Nair
MicroRNA Profile of Marek's Disease Virus-Transformed T-Cell Line MSB-1: Predominance of Virus-Encoded MicroRNAs
J. Virol., April 15, 2008; 82(8): 4007 - 4015.
[Abstract] [Full Text] [PDF]


Home page
J. Virol.Home page
J. Burnside, E. Bernberg, A. Anderson, C. Lu, B. C. Meyers, P. J. Green, N. Jain, G. Isaacs, and R. W. Morgan
Marek's Disease Virus Encodes MicroRNAs That Map to meq and the Latency-Associated Transcript.
J. Virol., September 1, 2006; 80(17): 8778 - 8786.
[Abstract] [Full Text] [PDF]


Home page
J. Virol.Home page
K. W. Jarosinski, N. Osterrieder, V. K. Nair, and K. A. Schat
Attenuation of Marek's Disease Virus by Deletion of Open Reading Frame RLORF4 but Not RLORF5a
J. Virol., September 15, 2005; 79(18): 11647 - 11659.
[Abstract] [Full Text] [PDF]


Home page
J. Virol.Home page
D. Schumacher, B. K. Tischer, W. Fuchs, and N. Osterrieder
Reconstitution of Marek's Disease Virus Serotype 1 (MDV-1) from DNA Cloned as a Bacterial Artificial Chromosome and Characterization of a Glycoprotein B-Negative MDV-1 Mutant
J. Virol., December 1, 2000; 74(23): 11088 - 11098.
[Abstract] [Full Text]


Home page
J. Virol.Home page
T. Yamaguchi, S. L. Kaplan, P. Wakenell, and K. A. Schat
Transactivation of Latent Marek's Disease Herpesvirus Genes in QT35, a Quail Fibroblast Cell Line, by Herpesvirus of Turkeys
J. Virol., November 1, 2000; 74(21): 10176 - 10186.
[Abstract] [Full Text]




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 © 1998 by the Society for General Microbiology.