Enhancement of Borna Disease Virus Transcription in Persistently Infected Cells by Serum Starvation.
- 1 January 1999
- journal article
- Published by Japanese Society of Veterinary Science in The Journal of Veterinary Medical Science
- Vol. 61 (7) , 831-834
- https://doi.org/10.1292/jvms.61.831
Abstract
Transcription of Borna disease virus (BDV) in persistently infected MDCK (MDCK/BDV) cells increased in the fetal bovine serum free media as detected by Northern blot analysis. Especially, the amount of 1.9-kb RNA without cap formation at the 5' end and polyadenylation at the 3' end, increased as compared to other mRNA molecules of BDV. Growth arrest of MDCK/BDV cells observed in the condition of serum starvation might be important for increasing viral transcription. Since N-cadherin is the responsible factor for cell-to-cell contact, MDCK/BDV cells were cultured in calcium free medium which inhibits the interaction of N-cadherin. However, inhibition of cell-to-cell contact by N-cadherin is not effective on up regulation of viral transcription. Our finding in this study indicates that enhancement of BDV transcription by serum starvation is a useful technique for further investigation in understanding of mechanisms of BDV transcription.Keywords
This publication has 10 references indexed in Scilit:
- Inhibition of Borna disease virus replication by ribavirin in persistently infected cells.Archiv für die gesamte Virusforschung, 1998
- Detection of a novel Borna disease virus-encoded 10 kDa protein in infected cells and tissues.Journal of General Virology, 1997
- Detection of Borna Disease Virus Antigen and RNA in Human Autopsy Brain Samples from Neuropsychiatric PatientsVirology, 1996
- The Remarkable Coding Strategy of Borna Disease Virus: A New Member of the Nonsegmented Negative Strand RNA VirusesVirology, 1995
- Natural and Experimental Borna Disease in AnimalsPublished by Springer Nature ,1995
- Initial Teacher Education: the pedagogy is the messageSouth Pacific Journal of Teacher Education, 1995
- Genomic organization of Borna disease virus.Proceedings of the National Academy of Sciences, 1994
- Human infections with Borna disease virus: Seroprevalence in patients with chronic diseases and healthy individualsJournal of Medical Virology, 1992
- Cell-cycle-directed regulation of thymidylate synthase messenger RNA in human diploid fibroblasts stimulated to proliferateJournal of Molecular Biology, 1986
- Replication of Borna disease virus in cell culturesMedical Microbiology and Immunology, 1980