Human cytomegalovirus latent infection and associated viral gene expression

Author:

Slobedman Barry1,Cao John Z1,Avdic Selmir1,Webster Bradley1,McAllery Samantha1,Cheung Allen KL1,Tan Joanne CG1,Abendroth Allison2

Affiliation:

1. Centre For Virus Research, Westmead Millennium Institute & University of Sydney, Westmead Millennium Institute, PO Box 412, New South Wales 2145, Australia

2. Department of Infectious Diseases & Immunology, University of Sydney, New South Wales 2006, Australia.

Abstract

Human cytomegalovirus (HCMV) is a clinically important and ubiquitous herpesvirus. Following primary productive infection the virus is not completely eliminated from the host, but instead establishes a lifelong latent infection without detectable virus production, from where it can reactivate at a later stage to generate new infectious virus. Reactivated HCMV often results in life-threatening disease in immunocompromised individuals, particularly allogeneic stem cell and solid organ transplant recipients, where it remains one of the most difficult opportunistic pathogens that complicate the care of these patients. The ability of HCMV to establish and reactivate from latency is central to its success as a human pathogen, yet latency remains very poorly understood. This article will cover several aspects of HCMV latency, with a focus on current understanding of viral gene expression and functions during this phase of infection.

Publisher

Future Medicine Ltd

Subject

Microbiology (medical),Microbiology

Reference135 articles.

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2. The Epidemiology and Prevention of Congenital Cytomegalovirus Infection and Disease: Activities of the Centers for Disease Control and Prevention Workgroup

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4. Two clinical isolates and the Toledo strain of cytomegalovirus contain endothelial cell tropic variants that are not present in the AD169, Towne, or Davis strains

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