Access count of this item: 252

Files in This Item:
File Description SizeFormat 
1348-0421.12193.pdf4.38 MBAdobe PDFView/Open
Title: Heat stress is a potent stimulus for enhancing rescue efficiency of recombinant Borna disease virus.
Authors: Kojima, Shohei
Honda, Tomoyuki
Matsumoto, Yusuke
Tomonaga, Keizo  kyouindb  KAKEN_id  orcid https://orcid.org/0000-0003-0405-7103 (unconfirmed)
Author's alias: 本田, 知之
Keywords: animal RNA virus
Borna disease virus
heat stress
viral vector
Issue Date: 2-Nov-2014
Publisher: wiley
Journal title: Microbiology and immunology
Volume: 58
Issue: 11
Start page: 636
End page: 642
Abstract: Recently developed vector systems based on Borna disease virus (BDV) hold promise as platforms for efficient and stable gene delivery to the central nervous system (CNS). However, because it currently takes several weeks to rescue recombinant BDV (rBDV), an improved rescue procedure would enhance the utility of this system. Heat stress reportedly enhances the rescue efficiency of other recombinant viruses. Here, heat stress was demonstrated to increase the amount of BDV genome in persistently BDV-infected cells without obvious cytotoxicity. Further analyses suggested that the effect of heat stress on BDV infection is not caused by an increase in the activity of BDV polymerase. More cells in which BDV replication occurs were obtained in the initial phase of rBDV rescue by using heat stress than when it was not used. Thus, heat stress is a useful improvement on the published rescue procedure for rBDV. The present findings may accelerate the practical use of BDV vector systems in basic science and the clinic and thus enable broader adoption of this viral vector, which is uniquely suited for gene delivery to the CNS.
Rights: This is the peer reviewed version of the following article: Kojima, S., Honda, T., Matsumoto, Y. and Tomonaga, K. (2014), Heat stress is a potent stimulus for enhancing rescue efficiency of recombinant Borna disease virus. Microbiology and Immunology, 58: 636–642, which has been published in final form at http://dx.doi.org/10.1111/1348-0421.12193. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Self-Archiving.
The full-text file will be made open to the public on 2 NOV 2015 in accordance with publisher's 'Terms and Conditions for Self-Archiving'.
この論文は出版社版でありません。引用の際には出版社版をご確認ご利用ください。
This is not the published version. Please cite only the published version.
URI: http://hdl.handle.net/2433/200269
DOI(Published Version): 10.1111/1348-0421.12193
PubMed ID: 25154584
Appears in Collections:Journal Articles

Show full item record

Export to RefWorks


Export Format: 


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.