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Table of Contents | March 2009

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Expression of the VP16 promoter following zosteriform spread of herpes simplex virus type 1.

Following infection of mice on the cornea, virus is transported through axons to the trigeminal ganglia, where it can travel through axons back to body surfaces (shown here as blue staining cells in the hair follicles of the mouse whisker pad). VP16 is normally expressed late and packaged into virions, where it initiates viral gene expression in the infected cell. Once latency is established in neurons, the stochastic derepression of VP16 is required to initiate viral reactivation (see Thompson et al.,doi:10.1371/journal.ppat.1000352).

Image Credit: Nancy M. Sawtell, Cincinnati Children's Hospital Medical Center

 
 

Opinion

New Disturbing Trend in Antimicrobial Resistance of Gram-Negative Pathogens

Jung Hun Lee, Seok Hoon Jeong, Sun-Shin Cha, Sang Hee Lee

 

Review

Where Are All the Mycobacterium avium Subspecies paratuberculosis in Patients with Crohn's Disease?

Ellen S. Pierce

 

Research Articles

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De Novo Synthesis of VP16 Coordinates the Exit from HSV Latency In Vivo

Richard L. Thompson, Chris M. Preston, Nancy M. Sawtell

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β-Lactam Resistance Response Triggered by Inactivation of a Nonessential Penicillin-Binding Protein

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