Journal article
The pros and cons of autophagic flux among herpesviruses
Autophagy, Vol.11(4), pp.716-717
04/03/2015
DOI: 10.1080/15548627.2015.1017223
PMCID: PMC4502768
PMID: 25905782
Abstract
Autophagy has been intensively studied in herpes simplex virus type 1 (HSV-1), a human alphaherpesvirus. The HSV-1 genome encodes a well-known neurovirulence protein called ICP34.5. When the gene encoding this protein is deleted from the genome, the virus is markedly less virulent when injected into the brains of animal models. Subsequent characterization of ICP34.5 established that the neurovirulence protein interacts with BECN1, thereby inhibiting autophagy and facilitating viral replication in the brain. However, an ortholog of the ICP34.5 gene is lacking in the genomes of other closely related alphaherpesviruses, such as varicella-zoster virus (VZV). Further, autophagosomes are easily identified in the exanthem (rash) that is the hallmark of both VZV diseases-varicella and herpes zoster. Inhibition of autophagy leads to diminished VZV titers. Finally, no block is detected in studies of autophagic flux following VZV infection. Thus autophagy appears to be proviral during VZV infection while antiviral during HSV-1 infection. Because divergence to this degree is extremely unusual for 2 closely related herpesviruses, we postulate that VZV has accommodated its infectious cycle to benefit from autophagic flux, whereas HSV-1 has captured cellular immunomodulatory genes to inhibit autophagy.
Details
- Title: Subtitle
- The pros and cons of autophagic flux among herpesviruses
- Creators
- Charles Grose - Virology Laboratory; Children's Hospital; University of IowaErin M Buckingham - Virology Laboratory; Children's Hospital; University of IowaWallen Jackson - Virology Laboratory; Children's Hospital; University of IowaJohn E Carpenter - Virology Laboratory; Children's Hospital; University of Iowa
- Resource Type
- Journal article
- Publication Details
- Autophagy, Vol.11(4), pp.716-717
- DOI
- 10.1080/15548627.2015.1017223
- PMID
- 25905782
- PMCID
- PMC4502768
- NLM abbreviation
- Autophagy
- ISSN
- 1554-8627
- eISSN
- 1554-8635
- Publisher
- Taylor & Francis
- Language
- English
- Date published
- 04/03/2015
- Academic Unit
- Stead Family Department of Pediatrics; Infectious Disease (Pediatrics)
- Record Identifier
- 9984093216002771
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