Epstein-Barr virus (EBV) and Kaposi's sarcoma herpesvirus (KSHV) are related human gammaherpesvirus and important pathogens in immunocompetent and immunosuppressed hosts. Oral transmission is the primary mechanism for EBV infection, and oral EBV infection is associated with nasopharyngeal carcinoma and oral hairy leukoplakia. The importance of oral transmission for KSHV infection remains to be determined, but persistent oral infection and oral virus shedding are common features for EBV and KSHV infections. However, in both instances oral viral infection is poorly understood including the cell types infected in the oral cavity, the viral genes important for oral transmission, primary infection and viral persistence, the role of oral epithelial cell versus lymphocyte infection, and the mucosal immune responses important for controlling oral infection. This program will combine virology, immunology, and pathology expertise to address fundamental issues in the oral biology of gammaherpesvirus infection in immunocompetent and immunosuppressed hosts. The recent discovery, cloning and sequencing of two gammaherpesviruses closely related to EBV and KSHV and naturally infecting rhesus macaques provide new experimental animal models wand will serve as a starting point to define the biology of oral gammaherpesvirus infection and to experimentally test the role of specific viral genes in vivo. Advances in defining KSHV-specific immune responses, mucosal immune responses to other viral antigens, and immune responses in the macaque animal model will be applied to better understand the immunology of oral gammaherpesvirus infections. An antibody core will develop new antibody reagents for these studies, and a pathology core will coordinate, develop, and apply innovative pathologic methods to study and detect oral viral infections. Translation of results from animal models to human studies is an important and intrinsic component of the program. This program will combine the comparative powers of studying closely related gammaherpesviruses with the synergy of clinicians, virologists, pathologist, and immunologist to better understand the oral pathogenesis of gammaherpesvirus infections in immunocompetent and immunosuppressed hosts.

Agency
National Institute of Health (NIH)
Institute
National Institute of Dental & Craniofacial Research (NIDCR)
Type
Research Program Projects (P01)
Project #
5P01DE014388-05
Application #
6934620
Study Section
Special Emphasis Panel (ZDE1-GH (46))
Program Officer
Nokta, Mostafa A
Project Start
2001-09-15
Project End
2007-08-31
Budget Start
2005-09-01
Budget End
2007-08-31
Support Year
5
Fiscal Year
2005
Total Cost
$1,342,294
Indirect Cost
Name
Brigham and Women's Hospital
Department
Type
DUNS #
030811269
City
Boston
State
MA
Country
United States
Zip Code
02115
Kawabata, Thomas; Weaver, James; Thomas, Dolca et al. (2012) Summary of roundtable discussion meeting: non-human primates to assess risk for EBV-related lymphomas in humans. J Immunotoxicol 9:121-7
Bilello, John P; Morgan, Jennifer S; Desrosiers, Ronald C (2008) Extreme dependence of gH and gL expression on ORF57 and association with highly unusual codon usage in rhesus monkey rhadinovirus. J Virol 82:7231-7
Cai, Xuezhong; Schafer, Alexandra; Lu, Shihua et al. (2006) Epstein-Barr virus microRNAs are evolutionarily conserved and differentially expressed. PLoS Pathog 2:e23
Bilello, John P; Lang, Sabine M; Wang, Fred et al. (2006) Infection and persistence of rhesus monkey rhadinovirus in immortalized B-cell lines. J Virol 80:3644-9
Fogg, Mark H; Garry, Deirdre; Awad, Amany et al. (2006) The BZLF1 homolog of an Epstein-Barr-related gamma-herpesvirus is a frequent target of the CTL response in persistently infected rhesus macaques. J Immunol 176:3391-401
Bilello, John P; Morgan, Jennifer S; Damania, Blossom et al. (2006) A genetic system for rhesus monkey rhadinovirus: use of recombinant virus to quantitate antibody-mediated neutralization. J Virol 80:1549-62
Chen, Adrienne; Divisconte, Matthew; Jiang, Xiaoqun et al. (2005) Epstein-Barr virus with the latent infection nuclear antigen 3B completely deleted is still competent for B-cell growth transformation in vitro. J Virol 79:4506-9
Fogg, Mark H; Kaur, Amitinder; Cho, Young-Gyu et al. (2005) The CD8+ T-cell response to an Epstein-Barr virus-related gammaherpesvirus infecting rhesus macaques provides evidence for immune evasion by the EBNA-1 homologue. J Virol 79:12681-91
Kutok, Jeffery L; Klumpp, Sherry; Simon, Meredith et al. (2004) Molecular evidence for rhesus lymphocryptovirus infection of epithelial cells in immunosuppressed rhesus macaques. J Virol 78:3455-61
Rivailler, Pierre; Carville, Angela; Kaur, Amitinder et al. (2004) Experimental rhesus lymphocryptovirus infection in immunosuppressed macaques: an animal model for Epstein-Barr virus pathogenesis in the immunosuppressed host. Blood 104:1482-9