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Journal of Virology, June 2007, p. 6106-6110, Vol. 81, No. 11
0022-538X/07/$08.00+0 doi:10.1128/JVI.00070-07
Copyright © 2007, American Society for Microbiology. All Rights Reserved.

Department of Ophthalmology (LSU Eye Center of Excellence),1 LSUHSC Neuroscience Center,2 Departments of Pharmacology and Microbiology, Louisiana State University Health Sciences Center at New Orleans, New Orleans, Louisiana3
Received 10 January 2007/ Accepted 2 March 2007
Recent studies have explored the chromatin structures associated with the herpes simplex virus type 1 (HSV-1) genome during latency, particularly with regard to specific histone tail modifications such as acetylation and dimethylation. The objective of our present study was to develop a rapid systemic method of in vivo HSV-1 reactivation to further explore the changes that occur in the chromatin structures associated with HSV-1 at early time points after the initiation of HSV reactivation. We present a uniform, rapid, and reliable method of in vivo HSV-1 reactivation in mice that yields high reactivation frequencies (75 to 100%) by using sodium butyrate, a histone deacetylase inhibitor, and demonstrate that the reactivating virus can be detected at the original site of infection.
Published ahead of print on 14 March 2007.
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