This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Supplemental material
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
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 arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Google Scholar
Right arrow Articles by Wang, F.
Right arrow Articles by McFadden, G.
PubMed
Right arrow PubMed Citation
Right arrow Articles by Wang, F.
Right arrow Articles by McFadden, G.

 Previous Article  |  Next Article 

Journal of Virology, June 2009, p. 5928-5932, Vol. 83, No. 11
0022-538X/09/$08.00+0     doi:10.1128/JVI.02587-08
Copyright © 2009, American Society for Microbiology. All Rights Reserved.

Induction of Alpha/Beta Interferon by Myxoma Virus Is Selectively Abrogated When Primary Mouse Embryo Fibroblasts Become Immortalized{triangledown} ,§

Fuan Wang,1,2,{dagger} John W. Barrett,1,2,{dagger} Yiyue Ma,1,2 Gregory A. Dekaban,1,2,{ddagger} and Grant McFadden1,3*

BioTherapeutics Research Group, Robarts Research Institute,1 Department of Microbiology and Immunology, The University of Western Ontario, London, Ontario, Canada,2 Department of Molecular Genetics and Microbiology, University of Florida, Gainesville, Florida3

Received 15 December 2008/ Accepted 13 March 2009

Mouse embryo fibroblasts (MEFs) are a widely used cell culture system in life sciences, including virology. Here, we show that although primary MEFs are nonpermissive to myxoma virus replication, the corresponding immortalized MEFs support a highly productive myxoma virus infection. We further demonstrate that this permissive phenotype for myxoma virus in immortalized MEFs is due to the immortalization-associated selective block to the cellular alpha/beta interferon induction machinery involved in responding to myxoma virus challenge. Thus, our report presents a clear example, illustrating that a drastic phenotypic alteration can occur with respect to virus infection between primary cells and their immortalized counterparts.


* Corresponding author. Mailing address: Department of Molecular Genetics and Microbiology, College of Medicine, University of Florida, 1600 SW Archer Rd., Academic Research Building, Room R4-295, P.O. Box 100266, Gainesville, FL 32610. Phone: (352) 273-6852. Fax: (352) 273-6849. E-mail: grantmcf{at}ufl.edu

{triangledown} Published ahead of print on 18 March 2009.

§ Supplemental material for this article may be found at http://jvi.asm.org/.

{dagger} These authors contributed equally to the work.

{ddagger} Co-senior author.


Journal of Virology, June 2009, p. 5928-5932, Vol. 83, No. 11
0022-538X/09/$08.00+0     doi:10.1128/JVI.02587-08
Copyright © 2009, American Society for Microbiology. All Rights Reserved.