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Journal of Virology, July 2003, p. 8159-8165, Vol. 77, No. 14
0022-538X/03/$08.00+0     DOI: 10.1128/JVI.77.14.8159-8165.2003
Copyright © 2003, American Society for Microbiology. All Rights Reserved.

Novel Kaposi's Sarcoma-Associated Herpesvirus Homolog in Baboons

Denise Whitby,1 Andrea Stossel,1 Christine Gamache,1 James Papin,2 Marnix Bosch,3 Anne Smith,4 Dean H. Kedes,4 Gary White,5 Ronald Kennedy,6 and Dirk P. Dittmer2*

Viral Epidemiology Section, AIDS Vaccine Program, SAIC-Frederick, National Cancer Institute—Frederick, Frederick, Maryland 21702,1 Department of Microbiology and Immunology,2 Department of Laboratory Animal Science, The University of Oklahoma Health Science Center, Oklahoma City, Oklahoma 73104,5 Northwest Hospital, Seattle, Washington,3 Departments of Microbiology and Internal Medicine, University of Virginia Health Systems, Charlottesville, Virginia,4 Department of Microbiology and Immunology, Texas Tech, Lubbock, Texas6

Received 10 January 2003/ Accepted 21 April 2003

Kaposi's sarcoma (KS) and lymphoproliferative diseases induced by KS-associated herpesvirus (KSHV/human herpesvirus 8) cause substantial morbidity and mortality in human immunodeficiency virus-infected individuals. To understand KSHV biology it is useful to investigate closely related rhadinoviruses naturally occurring in nonhuman primates. Here we report evidence for a novel KSHV homolog in captive baboon species (Papio anubis and other). Using degenerate PCR we identified a novel rhadinovirus, PapRV2, that has substantial sequence identity to two essential KSHV genes, the viral polymerase and thymidylate synthase. A subset of animals exhibited detectable PapRV2 viral load in peripheral blood mononuclear cells. Extensive serological analysis of nearly 200 animals in the colony demonstrated that the majority carried cross-reacting antibodies that recognize KSHV or macaque rhadinovirus antigens. Seroreactivity increased with age, similar to the age-specific prevalence of KSHV in the human population. This establishes baboons as a novel resource to investigate rhadinovirus biology, which can be developed into an animal model system for KSHV-associated human diseases, vaccine development, and therapy evaluation.


* Corresponding author. Mailing address: Department of Microbiology and Immunology, The University of Oklahoma Health Science Center, 940 Stanton L. Young Blvd., Oklahoma City, OK 73104. Phone: (405) 271-2690. Fax: (405) 271-3117. E-mail: dirk-dittmer{at}ouhsc.edu.


Journal of Virology, July 2003, p. 8159-8165, Vol. 77, No. 14
0022-538X/03/$08.00+0     DOI: 10.1128/JVI.77.14.8159-8165.2003
Copyright © 2003, American Society for Microbiology. All Rights Reserved.




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